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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Activity‐based probes for the ubiquitin conjugation–deconjugation machinery: new chemistries, new tools, and new insights</title>
<author><name sortKey="Hewings, David S" sort="Hewings, David S" uniqKey="Hewings D" first="David S." last="Hewings">David S. Hewings</name>
<affiliation><nlm:aff id="febs14039-aff-0001"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-aff-0002"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-aff-0003"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-aff-0004"></nlm:aff>
</affiliation>
</author>
<author><name sortKey="Flygare, John A" sort="Flygare, John A" uniqKey="Flygare J" first="John A." last="Flygare">John A. Flygare</name>
<affiliation><nlm:aff id="febs14039-aff-0001"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-curr-0001"></nlm:aff>
</affiliation>
</author>
<author><name sortKey="Bogyo, Matthew" sort="Bogyo, Matthew" uniqKey="Bogyo M" first="Matthew" last="Bogyo">Matthew Bogyo</name>
<affiliation><nlm:aff id="febs14039-aff-0004"></nlm:aff>
</affiliation>
</author>
<author><name sortKey="Wertz, Ingrid E" sort="Wertz, Ingrid E" uniqKey="Wertz I" first="Ingrid E." last="Wertz">Ingrid E. Wertz</name>
<affiliation><nlm:aff id="febs14039-aff-0002"></nlm:aff>
</affiliation>
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</affiliation>
</author>
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<idno type="pmid">28196299</idno>
<idno type="pmc">7163952</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7163952</idno>
<idno type="RBID">PMC:7163952</idno>
<idno type="doi">10.1111/febs.14039</idno>
<date when="2017">2017</date>
<idno type="wicri:Area/Pmc/Corpus">000914</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Activity‐based probes for the ubiquitin conjugation–deconjugation machinery: new chemistries, new tools, and new insights</title>
<author><name sortKey="Hewings, David S" sort="Hewings, David S" uniqKey="Hewings D" first="David S." last="Hewings">David S. Hewings</name>
<affiliation><nlm:aff id="febs14039-aff-0001"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-aff-0002"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-aff-0003"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-aff-0004"></nlm:aff>
</affiliation>
</author>
<author><name sortKey="Flygare, John A" sort="Flygare, John A" uniqKey="Flygare J" first="John A." last="Flygare">John A. Flygare</name>
<affiliation><nlm:aff id="febs14039-aff-0001"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-curr-0001"></nlm:aff>
</affiliation>
</author>
<author><name sortKey="Bogyo, Matthew" sort="Bogyo, Matthew" uniqKey="Bogyo M" first="Matthew" last="Bogyo">Matthew Bogyo</name>
<affiliation><nlm:aff id="febs14039-aff-0004"></nlm:aff>
</affiliation>
</author>
<author><name sortKey="Wertz, Ingrid E" sort="Wertz, Ingrid E" uniqKey="Wertz I" first="Ingrid E." last="Wertz">Ingrid E. Wertz</name>
<affiliation><nlm:aff id="febs14039-aff-0002"></nlm:aff>
</affiliation>
<affiliation><nlm:aff id="febs14039-aff-0003"></nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">The Febs Journal</title>
<idno type="ISSN">1742-464X</idno>
<idno type="eISSN">1742-4658</idno>
<imprint><date when="2017">2017</date>
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<front><div type="abstract" xml:lang="en"><p>The reversible post‐translational modification of proteins by ubiquitin and ubiquitin‐like proteins regulates almost all cellular processes, by affecting protein degradation, localization, and complex formation. Deubiquitinases (<styled-content style="fixed-case" toggle="no">DUB</styled-content>
s) are proteases that remove ubiquitin modifications or cleave ubiquitin chains. Most <styled-content style="fixed-case" toggle="no">DUB</styled-content>
s are cysteine proteases, which makes them well suited for study by activity‐based probes. These <styled-content style="fixed-case" toggle="no">DUB</styled-content>
probes report on deubiquitinase activity by reacting covalently with the active site in an enzyme‐catalyzed manner. They have proven to be important tools to study <styled-content style="fixed-case" toggle="no">DUB</styled-content>
selectivity and proteolytic activity in different settings, to identify novel <styled-content style="fixed-case" toggle="no">DUB</styled-content>
s, and to characterize deubiquitinase inhibitors. Inspired by the efficacy of activity‐based probes for <styled-content style="fixed-case" toggle="no">DUB</styled-content>
s, several groups have recently reported probes for the ubiquitin conjugation machinery (E1, E2, and E3 enzymes). Many of these enzymes, while not proteases, also posses active site cysteine residues and can be targeted by covalent probes. In this review, we will discuss how features of the probe (cysteine‐reactive group, recognition element, and reporter tag) affect reactivity and suitability for certain experimental applications. We will also review the diverse applications of the current probes, and discuss the need for new probe types to study emerging aspects of ubiquitin biology.</p>
</div>
</front>
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<biblStruct><analytic><author><name sortKey="Lawton, G" uniqKey="Lawton G">G Lawton</name>
</author>
</analytic>
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<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">FEBS J</journal-id>
<journal-id journal-id-type="iso-abbrev">FEBS J</journal-id>
<journal-id journal-id-type="doi">10.1111/(ISSN)1742-4658</journal-id>
<journal-id journal-id-type="publisher-id">FEBS</journal-id>
<journal-title-group><journal-title>The Febs Journal</journal-title>
</journal-title-group>
<issn pub-type="ppub">1742-464X</issn>
<issn pub-type="epub">1742-4658</issn>
<publisher><publisher-name>John Wiley and Sons Inc.</publisher-name>
<publisher-loc>Hoboken</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">28196299</article-id>
<article-id pub-id-type="pmc">7163952</article-id>
<article-id pub-id-type="doi">10.1111/febs.14039</article-id>
<article-id pub-id-type="publisher-id">FEBS14039</article-id>
<article-categories><subj-group subj-group-type="overline"><subject>Review Article</subject>
</subj-group>
<subj-group subj-group-type="heading"><subject>Special Issue: Proteases</subject>
<subj-group subj-group-type="heading"><subject>Review Articles</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group><article-title>Activity‐based probes for the ubiquitin conjugation–deconjugation machinery: new chemistries, new tools, and new insights</article-title>
<alt-title alt-title-type="left-running-head">D. S. Hewings <italic>et al</italic>
.</alt-title>
</title-group>
<contrib-group><contrib id="febs14039-cr-0001" contrib-type="author" corresp="yes"><name><surname>Hewings</surname>
<given-names>David S.</given-names>
</name>
<contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0001-9451-8959</contrib-id>
<xref ref-type="aff" rid="febs14039-aff-0001"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="febs14039-aff-0002"><sup>2</sup>
</xref>
<xref ref-type="aff" rid="febs14039-aff-0003"><sup>3</sup>
</xref>
<xref ref-type="aff" rid="febs14039-aff-0004"><sup>4</sup>
</xref>
<address><email>hewingsd@gene.com</email>
</address>
</contrib>
<contrib id="febs14039-cr-0002" contrib-type="author"><name><surname>Flygare</surname>
<given-names>John A.</given-names>
</name>
<xref ref-type="aff" rid="febs14039-aff-0001"><sup>1</sup>
</xref>
<xref ref-type="aff" rid="febs14039-curr-0001"><sup>5</sup>
</xref>
</contrib>
<contrib id="febs14039-cr-0003" contrib-type="author" corresp="yes"><name><surname>Bogyo</surname>
<given-names>Matthew</given-names>
</name>
<xref ref-type="aff" rid="febs14039-aff-0004"><sup>4</sup>
</xref>
<address><email>mbogyo@stanford.edu</email>
</address>
</contrib>
<contrib id="febs14039-cr-0004" contrib-type="author" corresp="yes"><name><surname>Wertz</surname>
<given-names>Ingrid E.</given-names>
</name>
<xref ref-type="aff" rid="febs14039-aff-0002"><sup>2</sup>
</xref>
<xref ref-type="aff" rid="febs14039-aff-0003"><sup>3</sup>
</xref>
<address><email>ingrid@gene.com</email>
</address>
</contrib>
</contrib-group>
<aff id="febs14039-aff-0001"><label><sup>1</sup>
</label>
<named-content content-type="organisation-division">Discovery Chemistry</named-content>
<institution>Genentech</institution>
<city>South San Francisco</city>
<named-content content-type="country-part">CA</named-content>
<country country="US">USA</country>
</aff>
<aff id="febs14039-aff-0002"><label><sup>2</sup>
</label>
<named-content content-type="organisation-division">Early Discovery Biochemistry</named-content>
<institution>Genentech</institution>
<city>South San Francisco</city>
<named-content content-type="country-part">CA</named-content>
<country country="US">USA</country>
</aff>
<aff id="febs14039-aff-0003"><label><sup>3</sup>
</label>
<named-content content-type="organisation-division">Discovery Oncology</named-content>
<institution>Genentech</institution>
<city>South San Francisco</city>
<named-content content-type="country-part">CA</named-content>
<country country="US">USA</country>
</aff>
<aff id="febs14039-aff-0004"><label><sup>4</sup>
</label>
<named-content content-type="organisation-division">Department of Pathology</named-content>
<institution>Stanford University School of Medicine</institution>
<named-content content-type="country-part">CA</named-content>
<country country="US">USA</country>
</aff>
<aff id="febs14039-curr-0001"><label><sup>5</sup>
</label>
Present address:<institution>Merck</institution>
<named-content content-type="street">630 Gateway Blvd</named-content>
<city>South San Francisco</city>
<named-content content-type="country-part">CA</named-content>
<postal-code>94080</postal-code>
<country country="US">USA</country>
</aff>
<author-notes><corresp id="correspondenceTo"><label>*</label>
<bold>Correspondence</bold>
<break></break>
D. S. Hewings, Discovery Chemistry, Genentech, South San Francisco, CA 94080, USA<break></break>
Tel: +1 650 225 3652<break></break>
E‐mail: <email>hewingsd@gene.com</email>
<break></break>
and<break></break>
I. E. Wertz, Discovery Oncology, Genentech, South San Francisco, CA 94080, USA<break></break>
Tel: +1 650 225 6222<break></break>
E‐mail: <email>ingrid@gene.com</email>
<break></break>
and<break></break>
M. Bogyo, Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA<break></break>
Fax: +1 650 725 7424<break></break>
Tel: +1 650 725 4132<break></break>
E‐mail: <email>mbogyo@stanford.edu</email>
<break></break>
</corresp>
</author-notes>
<pub-date pub-type="epub"><day>10</day>
<month>3</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="ppub"><month>5</month>
<year>2017</year>
</pub-date>
<volume>284</volume>
<issue>10</issue>
<issue-id pub-id-type="doi">10.1111/febs.2017.284.issue-10</issue-id>
<issue-title content-type="special-issue-title">Proteases and Proteolysis in Health and Disease</issue-title>
<fpage>1555</fpage>
<lpage>1576</lpage>
<history><date date-type="received"><day>09</day>
<month>11</month>
<year>2016</year>
</date>
<date date-type="rev-recd"><day>21</day>
<month>1</month>
<year>2017</year>
</date>
<date date-type="accepted"><day>10</day>
<month>2</month>
<year>2017</year>
</date>
</history>
<permissions><pmc-comment> Copyright © 2017 Federation of European Biochemical Societies </pmc-comment>
<copyright-statement content-type="article-copyright">© 2017 Federation of European Biochemical Societies</copyright-statement>
<license><license-p>This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="file:FEBS-284-1555.pdf"></self-uri>
<abstract id="febs14039-abs-0001"><p>The reversible post‐translational modification of proteins by ubiquitin and ubiquitin‐like proteins regulates almost all cellular processes, by affecting protein degradation, localization, and complex formation. Deubiquitinases (<styled-content style="fixed-case" toggle="no">DUB</styled-content>
s) are proteases that remove ubiquitin modifications or cleave ubiquitin chains. Most <styled-content style="fixed-case" toggle="no">DUB</styled-content>
s are cysteine proteases, which makes them well suited for study by activity‐based probes. These <styled-content style="fixed-case" toggle="no">DUB</styled-content>
probes report on deubiquitinase activity by reacting covalently with the active site in an enzyme‐catalyzed manner. They have proven to be important tools to study <styled-content style="fixed-case" toggle="no">DUB</styled-content>
selectivity and proteolytic activity in different settings, to identify novel <styled-content style="fixed-case" toggle="no">DUB</styled-content>
s, and to characterize deubiquitinase inhibitors. Inspired by the efficacy of activity‐based probes for <styled-content style="fixed-case" toggle="no">DUB</styled-content>
s, several groups have recently reported probes for the ubiquitin conjugation machinery (E1, E2, and E3 enzymes). Many of these enzymes, while not proteases, also posses active site cysteine residues and can be targeted by covalent probes. In this review, we will discuss how features of the probe (cysteine‐reactive group, recognition element, and reporter tag) affect reactivity and suitability for certain experimental applications. We will also review the diverse applications of the current probes, and discuss the need for new probe types to study emerging aspects of ubiquitin biology.</p>
</abstract>
<abstract abstract-type="graphical" id="febs14039-abs-0002"><p>E1, E2, E3, and deubiquitinating enzymes regulate protein ubiquitination, with profound consequences for protein stability and function. Therefore, there is considerable interest in developing approaches to study their activity. Activity‐based probes are valuable tools to understand the biochemical mechanisms and cellular functions of these enzymes.
<boxed-text position="anchor" content-type="graphic" id="febs14039-blkfxd-0001" orientation="portrait"><graphic xlink:href="FEBS-284-1555-g029.jpg" position="anchor" id="nlm-graphic-1" orientation="portrait"></graphic>
</boxed-text>
</p>
</abstract>
<kwd-group kwd-group-type="author-generated"><kwd id="febs14039-kwd-0001">activity‐based probe</kwd>
<kwd id="febs14039-kwd-0002">activity‐based protein profiling</kwd>
<kwd id="febs14039-kwd-0003">chemoproteomics</kwd>
<kwd id="febs14039-kwd-0004">deubiquitinase</kwd>
<kwd id="febs14039-kwd-0005">E1</kwd>
<kwd id="febs14039-kwd-0006">E3</kwd>
<kwd id="febs14039-kwd-0007">protease</kwd>
<kwd id="febs14039-kwd-0008">ubiquitin</kwd>
<kwd id="febs14039-kwd-0009">ubiquitin–proteasome system</kwd>
</kwd-group>
<counts><fig-count count="4"></fig-count>
<table-count count="2"></table-count>
<page-count count="22"></page-count>
<word-count count="13428"></word-count>
</counts>
<custom-meta-group><custom-meta><meta-name>source-schema-version-number</meta-name>
<meta-value>2.0</meta-value>
</custom-meta>
<custom-meta><meta-name>cover-date</meta-name>
<meta-value>May 2017</meta-value>
</custom-meta>
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<meta-value>Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.0 mode:remove_FC converted:15.04.2020</meta-value>
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</front>
<body id="febs14039-body-0001"><def-list list-content="abbreviations" id="febs14039-dl-0001"><title>Abbreviations</title>
<def-item><term>ABP</term>
<def><p>activity‐based probe</p>
</def>
</def-item>
<def-item><term>ABPP</term>
<def><p>activity‐based protein profiling</p>
</def>
</def-item>
<def-item><term>AOMK</term>
<def><p>acyloxymethyl ketone</p>
</def>
</def-item>
<def-item><term>Dha</term>
<def><p>dehydroalanine</p>
</def>
</def-item>
<def-item><term>DUB</term>
<def><p>deubiquitinase</p>
</def>
</def-item>
<def-item><term>HECT</term>
<def><p>homologous to the E6‐AP carboxyl terminus</p>
</def>
</def-item>
<def-item><term>MS</term>
<def><p>mass spectrometry</p>
</def>
</def-item>
<def-item><term>NEDD8</term>
<def><p>neural precursor cell expressed, developmentally down‐regulated 8</p>
</def>
</def-item>
<def-item><term>OTU</term>
<def><p>ovarian tumor domain protease</p>
</def>
</def-item>
<def-item><term>RBR</term>
<def><p>RING‐between‐RING</p>
</def>
</def-item>
<def-item><term>RING</term>
<def><p>really interesting new gene</p>
</def>
</def-item>
<def-item><term>SENP</term>
<def><p>SUMO‐specific protease</p>
</def>
</def-item>
<def-item><term>SUMO</term>
<def><p>small ubiquitin‐like modifier</p>
</def>
</def-item>
<def-item><term>Ubl</term>
<def><p>ubiquitin‐like protein</p>
</def>
</def-item>
<def-item><term>Ub</term>
<def><p>ubiquitin</p>
</def>
</def-item>
<def-item><term>UCH</term>
<def><p>ubiquitin C‐terminal hydrolase</p>
</def>
</def-item>
<def-item><term>ULP</term>
<def><p>Ubl protease</p>
</def>
</def-item>
<def-item><term>UPS</term>
<def><p>ubiquitin–proteasome system</p>
</def>
</def-item>
<def-item><term>USP</term>
<def><p>ubiquitin‐specific protease</p>
</def>
</def-item>
<def-item><term>VME</term>
<def><p>vinyl methyl ester</p>
</def>
</def-item>
<def-item><term>VS</term>
<def><p>vinyl sulfone</p>
</def>
</def-item>
</def-list>
<sec id="febs14039-sec-0001"><title>Ubiquitination: a dynamic multipurpose post‐translational modification</title>
<p>Since the discovery in the late 1970s and early 1980s that modification by ubiquitin targets proteins for degradation by the proteasome, the ubiquitin–proteasome system (UPS) has emerged as an essential regulator of almost all cellular processes in eukaryotes. Aside from maintaining proteostasis by degrading damaged or unwanted proteins, ubiquitination and subsequent degradation regulates the activity of many short‐lived proteins, including cell cycle regulators and transcription factors, and produces antigenic peptides for presentation on the cell surface <xref rid="febs14039-bib-0001" ref-type="ref">1</xref>
, <xref rid="febs14039-bib-0002" ref-type="ref">2</xref>
. Ubiquitination also has many proteasome‐independent roles, including regulating DNA damage repair, receptor endocytosis, and inflammation <xref rid="febs14039-bib-0003" ref-type="ref">3</xref>
. Not surprisingly, dysregulation of the UPS contributes to many illnesses, including cancer, neurodegenerative diseases, and immunological disorders.</p>
<p>Ubiquitin (Ub) is a small (8.5 kDa) globular protein of 76 amino acids that adopts a beta‐grasp fold (Fig. <xref rid="febs14039-fig-0001" ref-type="fig">1</xref>
A). It is highly conserved and found in all eukaryotes. Ub is attached to substrates through its terminal glycine residue, a process referred to as ubiquitination (or ubiquitylation) <xref rid="febs14039-bib-0004" ref-type="ref">4</xref>
. Typically, Ub is attached to proteins via an isopeptide bond to a lysine side chain, but proteins may also be ubiquitinated on their N terminus via a peptide bond. Ub itself can be ubiquitinated (polyubiquitination), giving rise to Ub chains <xref rid="febs14039-bib-0005" ref-type="ref">5</xref>
. This can occur through one of seven Lys residues (K6, K11, K27, K29, K33, K48, and K63) or the N‐terminal Met residue (M1). K48‐linked polyubiquitination is the best‐known and most‐studied modification, as it targets proteins to the proteasome for degradation <xref rid="febs14039-bib-0006" ref-type="ref">6</xref>
. Other chain types typically have signaling roles: for example, M1‐linked (also called linear) chains are important in several immune signaling pathways <xref rid="febs14039-bib-0007" ref-type="ref">7</xref>
, <xref rid="febs14039-bib-0008" ref-type="ref">8</xref>
.</p>
<fig fig-type="Figure" xml:lang="en" id="febs14039-fig-0001" orientation="portrait" position="float"><label>Figure 1</label>
<caption><p>Ubiquitin conjugation and deconjugation machinery. (A) X‐ray crystal structure of human ubiquitin (<styled-content style="fixed-case" toggle="no">PDB</styled-content>
: <ext-link ext-link-type="uri" xlink:href="http://www.rcsb.org/pdb/search/structidSearch.do?structureId=1UBI">http://www.rcsb.org/pdb/search/structidSearch.do?structureId=1UBI</ext-link>
). Lysine side chains are shown in magenta, N‐terminal methionine (M1) shown in cyan, and C‐terminal di‐Gly shown in blue; (B) overview of enzymes involved in Ub conjugation and deconjugation, with catalytic Cys residues indicated; (C) the ‘three Rs’ of an activity‐based probe (<styled-content style="fixed-case" toggle="no">ABP</styled-content>
)—reactive group, recognition element, and reporter tag—and the reaction of an <styled-content style="fixed-case" toggle="no">ABP</styled-content>
with an enzyme containing an active site Cys residue, such as a Cys protease.</p>
</caption>
<graphic id="nlm-graphic-3" xlink:href="FEBS-284-1555-g001"></graphic>
</fig>
<p>Ubiquitin is the archetypal example of a group of beta‐grasp proteins, referred to as ubiquitin‐like proteins (UBLs). In humans, these include the SUMO (small ubiquitin‐like modifier) family of proteins, NEDD8 (neural precursor cell expressed, developmentally down‐regulated 8), and several homologs of yeast Atg8 (autophagy‐related protein 8). Different conjugation and deconjugation machineries exist for the UBLs although there appears to be considerable overlap, with some enzymes functioning on several classes of UBL <xref rid="febs14039-bib-0009" ref-type="ref">9</xref>
, <xref rid="febs14039-bib-0010" ref-type="ref">10</xref>
. Prokaryotes do not encode for Ub, but do produce Ub‐like small protein modifiers that can be attached enzymatically to target proteins. The function of these modifiers is not fully understood <xref rid="febs14039-bib-0011" ref-type="ref">11</xref>
, but in some instances, such as the prokaryotic ubiquitin‐like protein (Pup) of <italic>Mycobacterium tuberculosis</italic>
, they can direct proteins for proteasomal degradation <xref rid="febs14039-bib-0012" ref-type="ref">12</xref>
.</p>
<p>Ubiquitination is a dynamic modification, with a dedicated system of enzymes responsible for transferring Ub to substrates, and proteases responsible for removing it. Ub conjugation requires the sequential action of three classes of enzymes (Fig. <xref rid="febs14039-fig-0001" ref-type="fig">1</xref>
B). E1 enzymes initially activate free ubiquitin in a two‐step mechanism. In the first step, the E1 enzyme binds Ub and ATP, and catalyzes Ub C‐terminal acyl‐adenylation to form E1:Ub~AMP. (The tilde [~] is used to indicate a reactive covalent bond, while the colon [:] indicates a noncovalent complex.) In the second step, Ub is transferred onto a Cys residue to form a thioether linkage (E1~Ub). Activated Ub is next transferred to the Cys residue of a Ub‐conjugating (sometimes referred to as Ub‐carrier) enzyme, E2, to give E2~Ub. E2s, together with Ub ligases (E3), then transfer Ub to the substrate. E3s confer substrate specify to the E2 enzymes. The cullin‐RING ligases, which are the largest group of E3s, do not form a covalent bond to Ub. However, two smaller groups, the HECT ligases (~ 30 members) and RBR ligases (~ 12 members) accept Ub from E2s to form a Ub‐thioester (E3~Ub), which then transfers Ub to a substrate <xref rid="febs14039-bib-0013" ref-type="ref">13</xref>
, <xref rid="febs14039-bib-0014" ref-type="ref">14</xref>
.</p>
<p>Deubiquitinases (DUBs) are proteases that hydrolyze the amide bond between the C‐terminal Gly residue of Ub and ubiquitinated proteins, thereby antagonizing the Ub conjugation machinery <xref rid="febs14039-bib-0015" ref-type="ref">15</xref>
. As well as rescuing proteins from degradation and reversing signaling events induced by ubiquitination, certain DUBs cleave Ub gene products into individual Ub monomers prior to activation by E1s <xref rid="febs14039-bib-0016" ref-type="ref">16</xref>
. The proteasome 19S regulatory particle also contains three DUBs (POH1, USP14, and UCHL5), which ‘recycle’ Ub by removing it from proteins prior to degradation. POH1 (PSMD14, RPN11) is located close to the entrance to the 20S core, and promotes substrate degradation by cleaving entire Ub chains from substrates, allowing the protein to enter the pore for degradation. By contrast, USP14 and UCHL5 are located further from the 20S core and antagonize degradation by removing Ub in a stepwise manner from the distal end, promoting substrate dissociation from the proteasome <xref rid="febs14039-bib-0017" ref-type="ref">17</xref>
.</p>
<p>The human genome encodes for approximately 90 DUBs, which fall into six classes <xref rid="febs14039-bib-0018" ref-type="ref">18</xref>
, <xref rid="febs14039-bib-0019" ref-type="ref">19</xref>
. Five classes are papain‐type Cys proteases: the ubiquitin‐specific proteases (USPs), ubiquitin C‐terminal hydrolases (UCHs), ovarian tumor domain proteases (OTUs), Machado–Joseph disease domain proteases (MJDs or Josephins), and motif interacting with ubiquitin‐containing novel DUB family (MINDY) DUBs. The sixth class of DUBs, JAB1/MPN/MOV34 (JAMMs, also known as MPN+), are zinc‐dependent metalloproteases.</p>
<p>Enzymes that attach and remove Ub have attracted significant interest as therapeutic targets. The NEDD8 E1 inhibitor MLN4924 (pevonedistat) is in Phase II trials for leukemia (ClinicalTrials.gov identifier: NCT02610777), and Ub E1 inhibitor MLN7243 has also recently entered clinical trials (ClinicalTrials.gov identifier: NCT02045095). Immunomodulatory imide drugs (IMiDs) such as thalidomide are known to target the cullin‐RING E3 cereblon, and are approved in hematological malignancies <xref rid="febs14039-bib-0020" ref-type="ref">20</xref>
. Several classes of compound that target the Ub ligase MDM2 are now in clinical trials <xref rid="febs14039-bib-0021" ref-type="ref">21</xref>
. These compounds antagonize the interaction of MDM2 with its substrate, the tumor suppressor p53, thereby increasing p53 stability. Antagonists of the inhibitor of apoptosis (IAP) family of E3 proteins have also entered clinical trials <xref rid="febs14039-bib-0022" ref-type="ref">22</xref>
. Recently, a DUB inhibitor (VLX1570) has entered Phase I trials for multiple myeloma (ClinicalTrials.gov identifier: NCT02372240). Tools to study the activity of the Ub conjugation and deconjugation machinery are therefore valuable not only to better understand the functions of these enzymes but also to identify and characterize new inhibitors.</p>
</sec>
<sec id="febs14039-sec-0002"><title>Activity‐based probes</title>
<p>Enzyme activity is tightly controlled at a post‐translational level. This allows cells to respond rapidly to stimuli, and to avoid unwanted activation of enzymatic activity. Many proteases are secreted in inactive forms and must undergo activation, either irreversibly (e.g., by proteolysis) or reversibly (e.g., by phosphorylation, formation of complexes with other proteins, pH change, or change in localization). Protein expression, as indicated by western blot or proteomics techniques, cannot therefore be used reliably to infer enzyme activity. Turnover of the natural substrate provides a direct measurement of activity but requires detection of the reaction products, which may be challenging in a complex cellular environment. Additionally, different enzymes often process the same substrate, making it difficult to assign activity to a particular enzyme. Activity‐based probes (ABPs) mimic substrate, but rather than being processed by the enzyme, they become covalently attached to the active site in an enzyme‐catalyzed reaction. As ABPs do not react with inactive enzymes, the extent of probe labeling is an indirect measure of enzyme activity. ABPs are particularly well suited for studying enzymes with nucleophilic catalytic residues, as a reactive electrophile can be incorporated into the probe to react covalently with the nucleophile. Consequently, cysteine, threonine, and serine proteases have been extensively studied with ABPs <xref rid="febs14039-bib-0023" ref-type="ref">23</xref>
.</p>
<p>An ABP consists of three components—‘three Rs’ (Fig. <xref rid="febs14039-fig-0001" ref-type="fig">1</xref>
C):</p>
<p><list list-type="bullet" id="febs14039-list-0001"><list-item><p>A reactive group. For enzymes with active site nucleophiles, this is an electrophile, often referred to as a ‘warhead’. The choice of reactive group will affect both the reactivity and selectivity of the probe.</p>
</list-item>
<list-item><p>A recognition element (targeting group). This confers selectivity toward the target of interest, and may be a small‐molecule inhibitor, a short peptide, or a full‐length protein.</p>
</list-item>
<list-item><p>A reporter tag (also referred to as a handle or label), for detection of probe‐labeled proteins. Fluorophores facilitate rapid and sensitive detection, while affinity labels (such as biotin or a peptide epitope) also allow for isolation and enrichment of labeled proteins. Alternatively, a small bioorthogonal group <xref rid="febs14039-bib-0024" ref-type="ref">24</xref>
such as an alkyne or azide may be included in the probe to allow subsequent attachment of a reporter. This is often referred to as ‘two‐step’ labeling, and may be particularly advantageous when larger tags interfere with reactivity, selectivity, or physiochemical properties of the probe. Some large ABPs, particularly the DUB probes described below, substantially increase the molecular weight of the target protein, so a mass shift on an SDS/PAGE gel can be used as an indication of probe labeling.</p>
</list-item>
</list>
</p>
<p>Activity‐based probes differ from substrate‐based probes, which lack the reactive group that becomes covalently attached to the active site. Fluorogenic substrates are frequently used as protease probes, and as they are turned over by the enzyme, they are very useful for kinetic studies. However, it is difficult to assign substrate turnover to the activity of a particular protease. ABPs overcome this limitation by forming a covalent bond to the target enzyme, and are therefore a powerful tool to identify and isolate the labeled protease. This is a major advantage when studying enzyme families with overlapping substrate selectivity, such as DUBs. A more detailed comparison of substrate‐based and activity‐based probes has been presented in a recent review <xref rid="febs14039-bib-0023" ref-type="ref">23</xref>
. Broad‐spectrum ABPs can be used to study activity of many members of a protein class simultaneously, a technique referred to as activity‐based protein profiling (ABPP) <xref rid="febs14039-bib-0025" ref-type="ref">25</xref>
.</p>
<p>The Ub conjugation and deconjugation machinery is uniquely suited for study using ABPs, due to the prevalence of enzymes with active site nucleophiles. Most DUBs are Cys proteases, and ABPs bearing Cys‐targeting electrophiles have proven to be powerful tools to identify DUBs, study the activity and selectivity of DUB inhibitors, characterize DUB enzymatic activity, and determine the physiological roles of this protease family. Additionally, E1, E2, and some E3 enzymes employ catalytic Cys residues to transfer Ub, which has recently been exploited to develop ABPs. In this review, we will focus on the design and application of ABPs for DUBs. We will also discuss the recent development of ABPs for the ubiquitin‐conjugating machinery (E1, E2, and E3 enzymes). Although these enzymes are not proteases, their probes share many similar features to the DUB ABPs.</p>
</sec>
<sec id="febs14039-sec-0003"><title>Deubiquitinases</title>
<p>In the 15 years since the development of the first covalent DUB ABP <xref rid="febs14039-bib-0026" ref-type="ref">26</xref>
, many different probe designs have been reported, differing in reporter tag and reactive group, but typically using one or more full‐length ubiquitin moieties as the recognition element. Four configurations of recognition element, electrophile, and label have been described (Fig. <xref rid="febs14039-fig-0002" ref-type="fig">2</xref>
A). The development of ABPs with such a variety of structures has occurred concurrently with the development of new techniques to synthesize modified ubiquitin, which have been the subject of several excellent reviews <xref rid="febs14039-bib-0027" ref-type="ref">27</xref>
, <xref rid="febs14039-bib-0028" ref-type="ref">28</xref>
, <xref rid="febs14039-bib-0029" ref-type="ref">29</xref>
, <xref rid="febs14039-bib-0030" ref-type="ref">30</xref>
. Recently, a DUB ABP employing a small molecule as a recognition element has been described, and is discussed in more detail below <xref rid="febs14039-bib-0031" ref-type="ref">31</xref>
.</p>
<fig fig-type="Figure" xml:lang="en" id="febs14039-fig-0002" orientation="portrait" position="float"><label>Figure 2</label>
<caption><p>(A) <styled-content style="fixed-case" toggle="no">DUB</styled-content>
probe designs. Almost all <styled-content style="fixed-case" toggle="no">DUB ABP</styled-content>
s contain one (designs i and ii) or two (designs iii and iv) full‐length Ub proteins, with an electrophile (E) positioned at the site of the scissile bond. The reporter tag is typically at the N terminus (designs i, iii, and iv) but may be located at the C terminus, attached to the electrophile (design ii); (B) reaction between a <styled-content style="fixed-case" toggle="no">DUB</styled-content>
active site Cys and probe electrophiles. Mechanistically, the reactions can be classified as direct addition (e.g., Ub‐<styled-content style="fixed-case" toggle="no">PA</styled-content>
), conjugate addition (e.g., Ub‐<styled-content style="fixed-case" toggle="no">VS</styled-content>
), or nucleophilic displacement (e.g., Ub‐Br2).</p>
</caption>
<graphic id="nlm-graphic-5" xlink:href="FEBS-284-1555-g002"></graphic>
</fig>
<sec id="febs14039-sec-0004"><title>Mono‐ubiquitin probes</title>
<sec id="febs14039-sec-0005"><title>Reactive group</title>
<p>The first ABPs to be developed for DUBs contain a single full‐length ubiquitin with an electrophile in place of the C‐terminal Gly residue (G76) <xref rid="febs14039-bib-0026" ref-type="ref">26</xref>
, <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
. Ubiquitin‐aldehyde (Ubal) and ubiquitin‐nitrile (Ub‐CN) were important tools in early mechanistic studies of DUBs <xref rid="febs14039-bib-0033" ref-type="ref">33</xref>
, notably being used to demonstrate that ubiquitin C‐terminal hydrolases form a covalent intermediate during catalysis <xref rid="febs14039-bib-0034" ref-type="ref">34</xref>
, <xref rid="febs14039-bib-0035" ref-type="ref">35</xref>
. Ubal was also used to solve the first structure of a DUB in complex with Ub <xref rid="febs14039-bib-0036" ref-type="ref">36</xref>
, revealing the conformational changes associated with Ub binding. However, the modification of DUBs by Ubal and Ub‐CN is reversible, and is not compatible with the strongly reducing conditions of SDS/PAGE <xref rid="febs14039-bib-0033" ref-type="ref">33</xref>
.</p>
<p>To overcome the limitations of these probes, Borodovsky <italic>et al</italic>
. developed the first irreversible DUB ABPs by introducing a C‐terminal vinyl methyl sulfone (VS). The probe labeled DUBs in cell lysates, and could be detected following SDS/PAGE due to the presence of an HA tag on the probe <xref rid="febs14039-bib-0026" ref-type="ref">26</xref>
. Related Ubl‐VS probes for NEDD8, ISG‐15, SUMO‐1, GATE‐16, GABARAP, MAP1‐LC3, and Apg8L were reported shortly thereafter <xref rid="febs14039-bib-0010" ref-type="ref">10</xref>
, <xref rid="febs14039-bib-0037" ref-type="ref">37</xref>
. A wide range of C‐terminal electrophiles have since been investigated, as summarized in Table <xref rid="febs14039-tbl-0001" ref-type="table">1</xref>
. Electrophiles are classified according to the nature of the reaction with the catalytic Cys (Fig. <xref rid="febs14039-fig-0002" ref-type="fig">2</xref>
B). Vinyl methyl sulfones and vinyl methyl esters (VME) have been widely employed, with Ub‐VME showing slightly greater reactivity <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
. Propargyl amides also react with DUB active site Cys residues, forming a vinyl thioether <xref rid="febs14039-bib-0038" ref-type="ref">38</xref>
, <xref rid="febs14039-bib-0039" ref-type="ref">39</xref>
. This surprising reaction appears to proceed via direct nucleophilic attack on the internal alkyne carbon, facilitated by stabilization of the developing carbanion by the ‘oxyanion hole’ of the active site <xref rid="febs14039-bib-0040" ref-type="ref">40</xref>
. The resulting adduct was stable to denaturing and reducing conditions, but could be cleaved in acid, which is useful for proteomic studies. (An acid‐cleavable conjugate formed between an E1 and an ABP is discussed below <xref rid="febs14039-bib-0041" ref-type="ref">41</xref>
.) Note that conjugate addition to electrophiles such as VS or VME is in principle reversible under basic conditions, but this does not appear to occur under the conditions in which these probes are used.</p>
<table-wrap id="febs14039-tbl-0001" xml:lang="en" orientation="portrait" position="float"><label>Table 1</label>
<caption><p>Cysteine‐reactive electrophiles employed in mono‐Ub/Ubl ABPs. Widely employed, commercially available probes are highlighted in red. Ub implies Ub<sub>1–75</sub>
(i.e., without the C‐terminal Gly), unless otherwise indicated. Note that two probes have been referred to as ‘Ub‐CN’. For some SUMO probes, only short peptides have been used, rather than full‐length protein: <sup>i</sup>
: QTGG; <sup>ii</sup>
: FQQQTGG</p>
</caption>
<table frame="hsides" rules="groups"><col style="border-right:solid 1px #000000" span="1"></col>
<col style="border-right:solid 1px #000000" span="1"></col>
<col style="border-right:solid 1px #000000" span="1"></col>
<col style="border-right:solid 1px #000000" span="1"></col>
<col style="border-right:solid 1px #000000" span="1"></col>
<thead valign="top"><tr style="border-bottom:solid 1px #000000"><th align="left" colspan="5" valign="top" rowspan="1"><italic>Native ubiquitin conjugate</italic>
<inline-graphic xlink:href="FEBS-284-1555-g005.jpg" xlink:title="image"></inline-graphic>
</th>
</tr>
<tr style="border-bottom:solid 1px #000000"><th align="left" valign="top" rowspan="1" colspan="1">Reaction type</th>
<th align="left" valign="top" rowspan="1" colspan="1">Cys‐reactive electrophile</th>
<th align="left" valign="top" rowspan="1" colspan="1">Structure</th>
<th align="left" valign="top" rowspan="1" colspan="1">Abbreviation</th>
<th align="left" valign="top" rowspan="1" colspan="1">References</th>
</tr>
</thead>
<tbody><tr><td align="left" rowspan="3" colspan="1">Direct (1,2) addition</td>
<td align="left" rowspan="1" colspan="1">Aldehyde</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g006.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ubal</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0033" ref-type="ref">33</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Nitrile</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g007.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐CN</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0033" ref-type="ref">33</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Propargyl amide</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g008.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐Prg/Ub‐PA</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0038" ref-type="ref">38</xref>
, <xref rid="febs14039-bib-0039" ref-type="ref">39</xref>
</td>
</tr>
<tr><td align="left" rowspan="7" colspan="1">Conjugate (1,4) addition</td>
<td align="left" rowspan="1" colspan="1">Vinyl methyl sulfone</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g009.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐VS</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0026" ref-type="ref">26</xref>
, <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Vinyl phenyl sulfone</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g010.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐VSPh</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Vinyl ethylsulfonate</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g011.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐OEtVS</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0042" ref-type="ref">42</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Vinyl methyl ester</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g012.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐VME</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Vinyl cyanide</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g013.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐VCN</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Thioacrylonitrile</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g014.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐CN</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0114" ref-type="ref">114</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Dehydroalanine</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g015.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐Dha‐<italic>N</italic>
‐methylamide</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0123" ref-type="ref">123</xref>
</td>
</tr>
<tr><td align="left" rowspan="7" colspan="1">Nucleophilic substitution</td>
<td align="left" rowspan="1" colspan="1">Chloroethylamine</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g016.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐Cl</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Bromoethylamine</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g017.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐Br2</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Bromopropylamine</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g018.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐Br3</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Acyloxymethyl ketone (AOMK)</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g019.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐TF<sub>3</sub>
BOK, VEA505<sup>i</sup>
</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0042" ref-type="ref">42</xref>
, <xref rid="febs14039-bib-0043" ref-type="ref">43</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Fluoromethyl ketone</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g020.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">SUMO‐FMK<sup>ii</sup>
</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0044" ref-type="ref">44</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">α‐Amino‐β‐lactone</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g021.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">Ub‐Lac</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0042" ref-type="ref">42</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Chloromethyl ketone</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g022.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">–</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0031" ref-type="ref">31</xref>
</td>
</tr>
</tbody>
</table>
<permissions><copyright-holder>John Wiley & Sons, Ltd</copyright-holder>
<license><license-p>This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.</license-p>
</license>
</permissions>
</table-wrap>
<p>Probes that react with the catalytic Cys by nucleophilic substitution have not been used widely, although a variety of leaving groups have been investigated <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
, <xref rid="febs14039-bib-0042" ref-type="ref">42</xref>
, <xref rid="febs14039-bib-0043" ref-type="ref">43</xref>
, <xref rid="febs14039-bib-0044" ref-type="ref">44</xref>
. Alkyl halides label a distinct, though more restricted, subset of DUBs compared to VS/VME electrophiles, and were important in the identification of OTU DUBs (discussed below) <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
. Acyloxymethyl ketones (AOMKs) are more reactive than VS/VME electrophiles, but show similar activity in lysate, perhaps due to their instability <xref rid="febs14039-bib-0042" ref-type="ref">42</xref>
, <xref rid="febs14039-bib-0043" ref-type="ref">43</xref>
. Consistent with its high reactivity toward Cys nucleophiles, the AOMK HA‐UbTF<sub>3</sub>
BOK labeled many E1, E2, and E3 enzymes in addition to DUBs <xref rid="febs14039-bib-0042" ref-type="ref">42</xref>
.</p>
<p>As Ub‐electrophile conjugates react with Cys residues on many non‐DUB proteins, should these molecules truly be regarded as ABPs? That is to say, do they target only active DUBs, or will they label DUBs regardless of whether the enzyme is in a catalytically active form? In several instances, DUB reactivity toward a probe has been shown to change after a stimulus without a change in DUB expression, suggesting the probe does indeed target only the active subpopulation of the enzyme. For example, treating cells with hydrogen peroxide reduces the labeling of some DUBs by Ub‐VS or Ub‐VME, due to oxidation of the catalytic Cys residue <xref rid="febs14039-bib-0045" ref-type="ref">45</xref>
, <xref rid="febs14039-bib-0046" ref-type="ref">46</xref>
. More revealingly, a study by Naik and Dixit showed that the catalytic activity of USP9X is activated by phosphorylation upon T‐cell receptor activation. Brief stimulation of T cells increased the labeling of USP9X by HA‐Ub‐VS without an increase in USP9X levels, while the phospho‐site mutant, which still possess a potentially reactive active site Cys residue, was much less reactive toward the probe following stimulation. Hence, the probe can distinguish between active and inactive forms of USP9X <xref rid="febs14039-bib-0047" ref-type="ref">47</xref>
.</p>
<p>Probe labeling could also give a misleading indication of activity if the reaction occurs on noncatalytic residues. In the case of OTUB1, HA‐Ub‐VS reacts preferentially at a noncatalytic Cys, so probe labeling does not indicate deubiquitinating activity <xref rid="febs14039-bib-0048" ref-type="ref">48</xref>
, but it is not clear if this is a more widespread phenomenon. Therefore, when interpreting experiments using Ub‐electrophile conjugates, researchers should be aware of the possibility of activity‐independent labeling arising from the electrophilic nature of the probe. As such, the proteins labeled with Ub‐electrophile conjugates are perhaps best referred to as ‘probe‐reactive’ rather than ‘active’.</p>
</sec>
<sec id="febs14039-sec-0006"><title>Reporter tag</title>
<p>Radioiodination <xref rid="febs14039-bib-0026" ref-type="ref">26</xref>
or nonspecific biotinylation <xref rid="febs14039-bib-0049" ref-type="ref">49</xref>
of a probe was initially used to detect probe‐reactive proteins. However, preparing the labeled probe is technically challenging and gives inhomogeneous labeling. Furthermore, radiolabeling does not allow for retrieval and identification of probe‐reactive proteins. These techniques have been supplanted by the use of N‐terminal epitope tags. The HA tag is widely used and has little effect on Ub recognition <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
, but other epitope tags have been used successfully: for example, FLAG‐NEDD8‐VS was used as an ABP to identify deneddylases, as HA‐NEDD8‐VS was insoluble <xref rid="febs14039-bib-0050" ref-type="ref">50</xref>
.</p>
<p>Epitope tags facilitate both detection and isolation of labeled proteins. For analysis of DUBs in lysates, detection of the tag by western blot allows rapid visualization of DUB activity. However, to relate the patterns seen in these blots to the activity of individual DUBs, proteins labeled in specific bands must be identified, usually by tandem MS. Additionally, the resolution of proteins by this technique is poor, and one apparent labeled protein in a gel may contain many labeled DUBs. To study the activity of specific DUBs, investigators frequently take advantage of the ~ 10 kDa increase in MW on probe labeling: by blotting for an individual DUB, and comparing the intensities of the larger (labeled) band to the smaller (unlabeled) band, the reactivity of the DUB toward the probe can be inferred. Affinity purification employing the epitope tag can be used to enrich labeled proteins, facilitating detection and identification of DUBs. The purified DUBs can be digested in solution and identified by tandem MS <xref rid="febs14039-bib-0051" ref-type="ref">51</xref>
, or initially resolved by SDS/PAGE followed by in‐gel digestion and MS identification <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
. In‐solution digestion procedures have the advantage of improved quantitation and detection of low‐abundance proteins, but require more complex analysis. A review of MS proteomic techniques in UPS research has been published recently <xref rid="febs14039-bib-0052" ref-type="ref">52</xref>
.</p>
<p>Developments in peptide synthesis and protein chemistry have allowed the incorporation of a range of labels at both the C and N termini. McGouran <italic>et al</italic>
. introduced probes containing a fluorophore (Cy5 or fluorescein) at the C terminus. In‐gel fluorescence gave better resolution of labeled proteins than anti‐HA immunoblotting, particularly for high MW proteins, as no transfer step is necessary prior to visualization, but the probe was somewhat less reactive than unmodified HA‐Ub‐VME. This was attributed to the size and charge of the fluorophore, which is positioned close to the DUB active site <xref rid="febs14039-bib-0053" ref-type="ref">53</xref>
. By contrast, probes with an N‐terminal fluorophore, as reported by de Jong <italic>et al</italic>
. <xref rid="febs14039-bib-0054" ref-type="ref">54</xref>
, showed the same activity toward DUBs as unmodified HA‐Ub‐VME. These N‐terminal conjugates were prepared by total chemical synthesis, allowing great flexibility in the choice of modification: a variety of dyes (Cy5 and TMR), affinity tags (HA, His<sub>6</sub>
, and biotin), and linkers (aminohexanoic acid, lysine, and photocleavable linker) could be incorporated by this method. Additionally, dual‐function probes were prepared, for example, containing both a biotin (for affinity purification of labeled DUBs) and a Cy5 (for fluorescence imaging). Claessen <italic>et al</italic>
. devised an alternative strategy for N‐terminal functionalization, which used ‘sortagging’ (i.e., sortase‐mediated ligation between appropriately tagged protein/peptide fragments) to introduce a biotin label. Additionally, they incorporated a chemically cleavable linker between biotin and the Ub N terminus. These linkers allowed elution and MS identification of probe‐reactive proteins after streptavidin–biotin affinity purification <xref rid="febs14039-bib-0055" ref-type="ref">55</xref>
.</p>
</sec>
<sec id="febs14039-sec-0007"><title>Recognition element</title>
<p>All DUBs must bind Ub close to the catalytic active site. Therefore, mono‐Ub can be employed as the recognition element in ABPs to target many DUBs, even those DUBs for which mono‐Ub is not the preferred substrate <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
. Full‐length ubiquitin is necessary for an effective reaction between probe and DUBs. This is in contrast to ABPs for many proteases, where only short peptide recognition elements are required. The requirement for full‐length ubiquitin results from several factors:</p>
<p><list list-type="bullet" id="febs14039-list-0002"><list-item><p>The catalytic domains of DUBs contain large Ub‐binding surfaces <xref rid="febs14039-bib-0056" ref-type="ref">56</xref>
. Many interactions therefore contribute to the affinity of DUBs for Ub, which are difficult to mimic with a small recognition element;</p>
</list-item>
<list-item><p>There is a short channel leading from the Ub‐binding surface to the active site. This provides selectivity for the C‐terminal tail of Ub and Ubls, but contributes only weakly to binding. For USP2, both the Ub ‘core’ and tail are required for binding: Ub C‐terminal peptides or Ub truncation mutants lacking any more than the C‐terminal Gly‐Gly motif showed negligible binding to the catalytic domain <xref rid="febs14039-bib-0057" ref-type="ref">57</xref>
;</p>
</list-item>
<list-item><p>Structural rearrangements in the DUB catalytic domain occur upon Ub binding. Many apo DUB catalytic domains are in catalytically inactive conformations <xref rid="febs14039-bib-0018" ref-type="ref">18</xref>
, and would be unreactive toward ABPs. Ub binding can bring active site residues into the correct alignment for catalysis, as occurs for USP7 <xref rid="febs14039-bib-0058" ref-type="ref">58</xref>
, or cause the translocation of surface loops that otherwise block the active site, as seem for USP14 <xref rid="febs14039-bib-0059" ref-type="ref">59</xref>
.</p>
</list-item>
</list>
</p>
<p>Borodovsky <italic>et al</italic>
. have investigated Ub and Ubl C‐terminal peptides as recognition elements for ABPs. They synthesized a range of VS‐containing peptides of varying lengths, based on the C termini of Ubls. Labeling in lysate by [<sup>125</sup>
I]‐Ub‐VS could only be inhibited by preincubation with high concentrations (> 50 μ<sc>m</sc>
) of a 12‐mer peptide based on the Ub C terminus, but shorter sequences were ineffective. By contrast, short recognition elements may be suitable for probes of SENP proteases that remove the ubiquitin‐like molecule SUMO from proteins <xref rid="febs14039-bib-0060" ref-type="ref">60</xref>
. It is not immediately apparent why SENP probes would require a much shorter recognition element than DUB probes. Borodovsky <italic>et al</italic>
. <xref rid="febs14039-bib-0060" ref-type="ref">60</xref>
note that SENPs recognize a smaller surface area of their substrate in the catalytic site compared to DUBs, and hence may be able to bind to shorter peptide sequences.</p>
</sec>
<sec id="febs14039-sec-0008"><title>Cellular permeability</title>
<p>Deubiquitinase/Ubl protease (ULP) ABPs are generally not cell‐permeable, due to their large recognition elements. Probe treatment must therefore be carried out on cell lysates. Preferably, DUBs would be labeled in their native cellular environment, so as not to disrupt subcellular localization, weak protein–protein interactions, and other factors that may affect DUB activity. Both pore‐forming toxins <xref rid="febs14039-bib-0055" ref-type="ref">55</xref>
and electroporation <xref rid="febs14039-bib-0061" ref-type="ref">61</xref>
have been used to deliver Ub‐containing probes to cells. Subsequent ABPP experiments were successful in both cases, but it is not clear whether this technique is more sensitive than labeling in lysates. Shorter recognition elements may improve cell permeability, but disappointingly small peptidic AOMK‐based inhibitors for SENPs did not appear to be cell‐permeable <xref rid="febs14039-bib-0043" ref-type="ref">43</xref>
.</p>
<p>Ward <italic>et al</italic>
. <xref rid="febs14039-bib-0031" ref-type="ref">31</xref>
recently described the first cell‐permeable DUB ABP. A high‐throughput screen for DUB inhibitors identified a chloromethylketone‐containing inhibitor of USP activity. To convert this into an ABP, the authors prepared an alkyne‐tagged analog (Table <xref rid="febs14039-tbl-0001" ref-type="table">1</xref>
). Competitive ABPP, in which intact U2OS cells were pretreated with varying concentrations of the untagged inhibitor followed by labeling with 125 n<sc>m</sc>
of probe, was used to identify specific probe targets. Twelve USPs were identified, of which nine could be competed away by excess unlabeled probe. The probe also labeled several recombinant USPs that are not expressed in U2OS cells. However, the probe targets many non‐DUB proteins, presumably through nonspecific reaction with reactive Cys residues.</p>
</sec>
</sec>
<sec id="febs14039-sec-0009"><title>Diubiquitin probes</title>
<p>The mono‐Ub ABPs described above rely solely on the interaction between Ub and the S1 site (which binds the Ub distal to the scissile bond) for affinity and specificity. While some DUBs, notably those of the UCH family, prefer to process Ub with only short C‐terminal extensions, most DUBs cleave Ub from ubiquitinated substrates. These substrates may be ubiquitin itself, or other proteins. DUBs can display specificity for position in the Ub chain (<italic>exo</italic>
,<italic> endo</italic>
, or base cleavage) or linkage type using additional Ub‐binding sites, which can recognize Ub on the distal side (S1, S2 sites) or proximal side (in S1′ sites) (Fig. <xref rid="febs14039-fig-0003" ref-type="fig">3</xref>
). Di‐Ub APBs have therefore been developed in order to study activity and linkage specify for such DUBs. Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
summarizes the di‐Ub probes reported to date, along with the linkage types that were studied with each probe type.</p>
<fig fig-type="Figure" xml:lang="en" id="febs14039-fig-0003" orientation="portrait" position="float"><label>Figure 3</label>
<caption><p>Deubiquitinases specificity. Ub‐binding sites in the <styled-content style="fixed-case" toggle="no">DUB</styled-content>
can convey specificity for: a particular linkage type such as K63‐ or K48‐linked chains (A); or position within the Ub chain (B) <xref rid="febs14039-bib-0018" ref-type="ref">18</xref>
.</p>
</caption>
<graphic id="nlm-graphic-7" xlink:href="FEBS-284-1555-g003"></graphic>
</fig>
<table-wrap id="febs14039-tbl-0002" xml:lang="en" orientation="portrait" position="float"><label>Table 2</label>
<caption><p>Designs of di‐Ub‐based ABPs</p>
</caption>
<table frame="hsides" rules="groups"><col style="border-right:solid 1px #000000" span="1"></col>
<col style="border-right:solid 1px #000000" span="1"></col>
<col style="border-right:solid 1px #000000" span="1"></col>
<col style="border-right:solid 1px #000000" span="1"></col>
<thead valign="top"><tr style="border-bottom:solid 1px #000000"><th align="left" valign="top" rowspan="1" colspan="1"></th>
<th align="left" valign="top" rowspan="1" colspan="1">Electrophile structure</th>
<th align="left" valign="top" rowspan="1" colspan="1">Linkages</th>
<th align="left" valign="top" rowspan="1" colspan="1">Reference</th>
</tr>
</thead>
<tbody><tr><td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g023.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">K48, K63</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0062" ref-type="ref">62</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g024.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">K48, K63</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0064" ref-type="ref">64</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">3</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g025.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">M1<xref ref-type="fn" rid="febs14039-note-0001">a</xref>
, K6, K11, K27, K29, K33, K48, K63</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0065" ref-type="ref">65</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">4</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g026.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">M1<xref ref-type="fn" rid="febs14039-note-0001">a</xref>
, K48, K63</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0066" ref-type="ref">66</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">5</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g027.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">K6, K11, K27, K29, K33, K48, K63</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0068" ref-type="ref">68</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">6</td>
<td align="left" rowspan="1" colspan="1"><inline-graphic xlink:href="FEBS-284-1555-g028.jpg" xlink:title="image"></inline-graphic>
</td>
<td align="left" rowspan="1" colspan="1">K6, K11, K27, K29, K33, K48, K63</td>
<td align="left" rowspan="1" colspan="1"><xref rid="febs14039-bib-0067" ref-type="ref">67</xref>
</td>
</tr>
</tbody>
</table>
<table-wrap-foot id="febs14039-ntgp-0001"><fn id="febs14039-note-0001"><label>a</label>
<p>Not an effective mimic of linear M1 linkage for DUBs (see discussion in text).</p>
</fn>
</table-wrap-foot>
<permissions><copyright-holder>John Wiley & Sons, Ltd</copyright-holder>
<license><license-p>This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.</license-p>
</license>
</permissions>
</table-wrap>
<p>The first di‐Ub ABPs were reported by Iphöfer <italic>et al</italic>
., who used short peptides conjugated through Lys isopeptide bonds to mimic the proximal Ub (structure 1, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) <xref rid="febs14039-bib-0062" ref-type="ref">62</xref>
. Probes mimicking K48‐ and K63‐linked di‐Ub showed the expected reactivity toward a small number of recombinant DUBs, and labeled different sets of DUBs in lysate, as determined by gel‐ and MS‐based ABPP experiments. It is apparent from structural studies, however, that some DUBs can make extensive contacts with proximal Ub in the S1′ site <xref rid="febs14039-bib-0063" ref-type="ref">63</xref>
; probes containing short peptides are therefore unlikely to recapitulate the reactivity and selectivity of full‐length di‐Ub. Subsequent efforts have therefore focused on making di‐Ub probes containing two intact Ub monomers.</p>
<p>Several groups have recently reported strategies to make full‐length di‐Ub probes, either by intein‐based semisynthesis using recombinant protein (structure 2, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) <xref rid="febs14039-bib-0064" ref-type="ref">64</xref>
or total chemical synthesis (structures 4–6, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) <xref rid="febs14039-bib-0065" ref-type="ref">65</xref>
, <xref rid="febs14039-bib-0066" ref-type="ref">66</xref>
, <xref rid="febs14039-bib-0067" ref-type="ref">67</xref>
. Generally, these probes show the expected reactivity toward DUBs with known linkage selectivity: for example, the generally unselective USP DUBs react with most probes, while the K48‐selective DUB OTUB1 reacts preferentially with K48‐mimicking probes. The activity of most probes was verified in lysate <xref rid="febs14039-bib-0062" ref-type="ref">62</xref>
, <xref rid="febs14039-bib-0064" ref-type="ref">64</xref>
, <xref rid="febs14039-bib-0065" ref-type="ref">65</xref>
, <xref rid="febs14039-bib-0067" ref-type="ref">67</xref>
, <xref rid="febs14039-bib-0068" ref-type="ref">68</xref>
.</p>
<p>While it appears these probes can effectively mimic chains linked via Ub Lys residues, it has proved challenging to develop probes mimicking M1 linear Ub. The triazole‐containing linkage employed by McGouran <italic>et al</italic>
. (structure 3, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) was designed to mimic an isopeptide linkage and is significantly longer and more flexible than the native M1 peptide linkage. It did not react with known M1‐specific DUB OTULIN, but did react with USP13, USP25, and USP40, which show little activity toward the M1 chains <italic>in vitro</italic>
<xref rid="febs14039-bib-0065" ref-type="ref">65</xref>
. The dehydroalanine‐containing M1 probe reported by Haj‐Yahya <italic>et al</italic>
. (structure 4, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) was cleaved by the M1‐specific DUBs OTULIN and USP2, rather than reacting covalently with the electrophile. The dehydroalanine was in the P1′ site, and it appears to be inaccessible to the catalytic Cys <xref rid="febs14039-bib-0066" ref-type="ref">66</xref>
.</p>
</sec>
<sec id="febs14039-sec-0010"><title>Uses of DUB ABPs</title>
<p>Deubiquitinase and ULP APBs have found extensive use in a wide variety of studies, but a comprehensive analysis of all the reported uses of such probes is beyond the scope of this review. Instead, we summarize the principal applications of these probes, highlighting some key publications and recent developments. In addition to the uses described below, covalent DUB inhibitors such as Ubal and Ub‐VME have been used in crystallographic studies to determine the structures of DUBs bound to their substrate <xref rid="febs14039-bib-0036" ref-type="ref">36</xref>
, <xref rid="febs14039-bib-0058" ref-type="ref">58</xref>
, <xref rid="febs14039-bib-0069" ref-type="ref">69</xref>
. However, only the recognition element and warhead are needed for this application. As a label is not required, these tools are not considered ABPs and will not be discussed further here.</p>
<sec id="febs14039-sec-0011"><title>Identification of novel DUBs</title>
<p>Activity‐based probes have proven to be invaluable tools to identify new DUBs and ULPs in a variety of organisms. In one of the earliest applications of ABPs to identify DUBs, Borodovsky <italic>et al</italic>
. used [<sup>125</sup>
I]‐Ubal to label DUBs in yeast and human cell lysates. The authors compared labeling in mutants lacking putative DUBs to identify labeled proteases. Comparison with labeling in human cells led to the identification of USP14 (the homolog of yeast Ubp6p) as a proteasome‐associated DUB <xref rid="febs14039-bib-0026" ref-type="ref">26</xref>
. However, this approach to identifying DUBs is cumbersome and requires prior knowledge of candidate proteins. The combination of tandem mass spectrometry (LC‐MS/MS) for protein identification, and tagged probes for enrichment of labeled proteins, has allowed DUBs to be identified with high sensitivity in an unbiased manner. Notably, ABPs were used to identify the OTU family of DUBs <xref rid="febs14039-bib-0032" ref-type="ref">32</xref>
, <xref rid="febs14039-bib-0070" ref-type="ref">70</xref>
.</p>
<p>Mono‐Ub ABPs have also been widely used to identify DUBs in pathogenic organisms, including viruses (<italic>Adenoviridae</italic>
<xref rid="febs14039-bib-0049" ref-type="ref">49</xref>
and <italic>Herpesviridae</italic>
<xref rid="febs14039-bib-0071" ref-type="ref">71</xref>
, <xref rid="febs14039-bib-0072" ref-type="ref">72</xref>
), bacteria (<italic>Chlamydia trachomatis</italic>
<xref rid="febs14039-bib-0055" ref-type="ref">55</xref>
, <xref rid="febs14039-bib-0073" ref-type="ref">73</xref>
, <italic>Legionella pneumophilia</italic>
<xref rid="febs14039-bib-0074" ref-type="ref">74</xref>
, and <italic>Escherichia coli</italic>
<xref rid="febs14039-bib-0075" ref-type="ref">75</xref>
), parasitic protozoa (<italic>Toxoplasma gondii</italic>
<xref rid="febs14039-bib-0076" ref-type="ref">76</xref>
and <italic>Plasmodium falciparum</italic>
<xref rid="febs14039-bib-0077" ref-type="ref">77</xref>
), and nematodes (<italic>Trichinella spiralis</italic>
<xref rid="febs14039-bib-0078" ref-type="ref">78</xref>
). Prokaryotes and viruses, unlike eukaryotic pathogens, lack their own ubiquitination machinery <xref rid="febs14039-bib-0079" ref-type="ref">79</xref>
. Therefore, pathogens have probably evolved this function in order to ‘hijack’ the host UPS, although some of these apparent DUBs may have preferred pathogenic substrates that happen to share some similarity with Ub/Ubl conjugates.</p>
<p>A recent study by Pruneda <italic>et al</italic>
. <xref rid="febs14039-bib-0080" ref-type="ref">80</xref>
has examined the deubiquitinating activity of multiple bacterial proteases. Using a combination of ABPs (Ub‐PA) <xref rid="febs14039-bib-0038" ref-type="ref">38</xref>
and fluorescent substrates <xref rid="febs14039-bib-0081" ref-type="ref">81</xref>
, the authors verified the deubiquitinase and/or deneddylase activity of several previously proposed bacterial DUBs and identified three novel enzymes (in <italic>Rickettsia bellii</italic>
,<italic> Shigella flexneri</italic>
, and <italic>Xanthomonas campestris</italic>
). Notably, these bacterial DUBs all belonged to the CE protease clan, which in humans is limited to deneddylases and desumoylases. As bacterial members of the CE clan can also act as acetyltransferases, it appears that a single catalytic fold has evolved in different organisms to perform remarkably diverse functions.</p>
</sec>
<sec id="febs14039-sec-0012"><title>Characterization of DUB selectivity</title>
<p>Using ABPs to examine DUB selectivity has only become possible since the development of di‐Ub ABPs. McGouran <italic>et al</italic>
. profiled DUB activity in cell lysate by tandem MS with a panel of di‐Ub probes, but differences in geometry between the native isopeptide linkage and the triazole linkage employed in the probe (structure 3, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) may alter reactivity <xref rid="febs14039-bib-0065" ref-type="ref">65</xref>
. Comprehensive MS‐based ABPP experiments with newer di‐Ub probes have not yet been reported.</p>
<p>Several recent examples highlight the potential of di‐Ub ABPs to study the linkage selectivity of DUBs. Studies on substrate selectivity have used di‐Ub <xref rid="febs14039-bib-0082" ref-type="ref">82</xref>
, or more recently, di‐Ub‐based ABPs with an internal electrophile (structure 5, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) <xref rid="febs14039-bib-0083" ref-type="ref">83</xref>
, <xref rid="febs14039-bib-0084" ref-type="ref">84</xref>
. These substrates allow analysis of S1–S1′ preferences, but do not provide any information on the effect of S2 sites (Fig. <xref rid="febs14039-fig-0002" ref-type="fig">2</xref>
A). Flierman <italic>et al</italic>
. used di‐Ub ABPs with a terminal electrophile (structure 6, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) in combination with di‐Ub substrate probes with a terminal fluorophore to study the effect of S2 sites <xref rid="febs14039-bib-0067" ref-type="ref">67</xref>
. They observed significant differences between S1–S1′ and S1–S2 selectivity for OTU DUBs. For example, OTUD2 is fairly promiscuous in cleaving di‐Ub substrates, but shows a preference for the K11‐linked di‐Ub terminal ABP, suggesting that the S2 pocket refines the selectivity of this DUB toward K11‐linked chains. OTUD3 can cleave both K6 and K11‐linked di‐Ub, but only reacts with the K11 di‐Ub probe. Kinetic studies using di‐Ub substrate probes (di‐Ub‐AMC) suggested that the selectivity of OTUD2 for longer K11‐linked chains is driven by affinity (lower K<sub>M</sub>
), while for OTUD3, it appears to be driven by v<sub>max</sub>
, hinting that binding of K11 chains to OTUD3 may optimally reorganize the active site for catalysis. As the authors note, different selectivities across the S1–S1′ and S1–S2 sites suggest that the preferred endogenous substrates for these DUBs may be heterotypic chains. Testing this hypothesis will require the development of tri‐Ub reagents with mixed linkage types.</p>
<p>A similar influence of S1–S2 preference is observed in the papain‐like protease of severe acute respiratory syndrome coronavirus (SARS PLpro). The enzyme is known to cleave K48‐linked polyubiquitin chains with a minimal preferred substrate of three Ub units, leading to the accumulation of diUb<sup>K48</sup>
<xref rid="febs14039-bib-0085" ref-type="ref">85</xref>
. To explore this striking selectivity, Békés <italic>et al</italic>
. compared reactivity of the enzyme toward K48‐linked di‐Ub probes with either an internal (structure 5, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
) or a distal electrophile (structure 6, Table <xref rid="febs14039-tbl-0002" ref-type="table">2</xref>
), and a mono‐Ub‐PA probe <xref rid="febs14039-bib-0086" ref-type="ref">86</xref>
. The enzyme reacted rapidly with the distal K48‐linked di‐Ub probe, slowly with Ub‐PA and very slowly with the internal di‐Ub probe. This led the authors to conclude that SARS PLpro recognizes the K48 linkage between two distal Ub (S1 and S2), while cleaving between S1 and S1′. (K48 specificity across S1–S1′ is much weaker than across S1–S2.) The distal K48‐linked di‐Ub probe was subsequently used in structural studies to understand how SARS PLpro binds K48‐linked di‐Ub. Taken together, these studies highlight the value of using ABPs in combination with other tools, including substrate probes, to study the complexities of DUB selectivity.</p>
</sec>
<sec id="febs14039-sec-0013"><title>Profiling DUB activity across different conditions or stimuli</title>
<p>Deubiquitinase ABPs can be used to identify changes in DUB activity under different conditions or in different cell types. Some of the first studies employing DUB APBs profiled DUB activity in tumor, normal, and virus‐infected cells <xref rid="febs14039-bib-0087" ref-type="ref">87</xref>
, and in pairs of normal and tumor biopsies from cervical carcinoma patients <xref rid="febs14039-bib-0088" ref-type="ref">88</xref>
. However, identifying consistent changes in the patterns of DUB activity was challenging, and the biological significance of the observed differences was unclear. Other studies have taken a more focused approach: applying a stimulus to cells, monitoring changes in DUB activity, identifying DUBs with large changes in activity, then validating their role in the system of interest. A notable example of this strategy is the identification of USP7 as a regulator of adipogenesis <xref rid="febs14039-bib-0089" ref-type="ref">89</xref>
. HA‐Ub‐VS was used to monitor changes in DUB activity in an <italic>in vitro</italic>
adipogenesis model, which identified a substantial increase in USP7 activity. Further experiments confirmed that USP7 was required for adipogenesis, and that it exerted its effect through the deubiquitniation and stabilization of the acetyltransferase Tip60, a key regulator of adipocyte differentiation.</p>
<p>This approach has also been used to study the effects of infection on host DUBs. Kummari <italic>et al</italic>
. <xref rid="febs14039-bib-0090" ref-type="ref">90</xref>
used HA‐Ub‐VS to profile DUB activity in Salmonella‐infected chicken macrophages, and identified several DUBs that change substantially in activity following infection. UCHL3 activity decreased (although protein levels remained similar), while the proteasome‐associated DUB UCHL5 increased in both activity and protein level. The authors went on to demonstrate that UCHL5 expression increases IL‐1β secretion, and increases the levels of caspase‐1, a key member of the inflammasome that processes pro‐IL‐1β into its active form. This study, and others <xref rid="febs14039-bib-0091" ref-type="ref">91</xref>
, point toward a role for DUBs such as UCHL5 in the innate immune response to bacterial infection, through modulation of inflammasome formation, cytokine section, and pyroptosis. The molecular mechanisms underlying the possible role of UCHL5 in inflammasome regulation, including the targets of deubiquitinase activity, are as yet unclear.</p>
<p>The studies highlighted here demonstrate the potential of ABPP to identify DUBs involved in cellular processes, exemplified here by differentiation or the innate immune response. ABPP offers an alternative approach to functional genomics techniques, such as overexpression <xref rid="febs14039-bib-0092" ref-type="ref">92</xref>
or siRNA <xref rid="febs14039-bib-0093" ref-type="ref">93</xref>
screens for DUBs. (Notably, overexpression screens have also identified USP7 as a Tip60 deubiquitinase <xref rid="febs14039-bib-0094" ref-type="ref">94</xref>
, and have identified DUBs involved in inflammasome formation <xref rid="febs14039-bib-0095" ref-type="ref">95</xref>
.) As ABPP measures endogenous DUB activity, it avoids the problems introduced by artificially overexpressing or reducing gene expression, such as changes in viability or off‐target effects. ABPP also has the advantage of experimental simplicity, as no transfection is required and DUB activity is measured in a single experiment, either a gel‐based assay or tandem MS. However, the activity of many DUBs may change between experimental and control conditions, and identifying those that are functionally relevant can be challenging. Additionally, ABPs are not equally reactive toward all DUBs, and so changes in activity of DUBs that are unreactive toward the probe (such as the metalloprotease JAMM/MPN+ family) will be missed.</p>
</sec>
<sec id="febs14039-sec-0014"><title>DUB inhibitor screening</title>
<p>Activity‐based protein profiling is widely used to assess inhibitor selectivity <xref rid="febs14039-bib-0096" ref-type="ref">96</xref>
. In a typical experiment, often referred to as competitive ABPP, cells are incubated with compounds of interest, then lysed and treated with an HA‐tagged APB. (Compound treatment can also be performed using lysate <xref rid="febs14039-bib-0097" ref-type="ref">97</xref>
.) Comparison with an untreated control indicates the level of inhibition. As with experiments to profile DUB activity in cells, gel‐based methods provide a rapid readout <xref rid="febs14039-bib-0097" ref-type="ref">97</xref>
, but this approach is at best semiquantitative, and identifying the compound's targets is challenging. Quantitative MS can overcome these limitations, at the expense of experimental simplicity <xref rid="febs14039-bib-0051" ref-type="ref">51</xref>
.</p>
<p>Notably, ABPP has been used to assess selectivity during the development of VLX1570, the only DUB inhibitor so far to progress to clinical trials <xref rid="febs14039-bib-0098" ref-type="ref">98</xref>
. The hit compound b‐AP15 was initially identified as an inducer of the lysosomal apoptosis pathway <xref rid="febs14039-bib-0099" ref-type="ref">99</xref>
, and was subsequently shown to inhibit the proteasome <xref rid="febs14039-bib-0100" ref-type="ref">100</xref>
. Gel‐based analysis of labeling by HA‐Ub‐VS showed little global effect of this compound on DUB activity at 1 μ<sc>m</sc>
, but labeling of the isolated 26S proteasome or 19S regulatory particle was inhibited. The 19S regulatory particle contains two Cys‐protease DUBs, USP14 and UCHL5, both of which are inhibited by this compound, with slightly greater inhibitory activity toward USP14 <xref rid="febs14039-bib-0100" ref-type="ref">100</xref>
. VLX1570 showed similar selectivity toward USP14 and UCHL5, a finding confirmed by conventional inhibition assays using recombinant DUBs and a fluorogenic substrate <xref rid="febs14039-bib-0101" ref-type="ref">101</xref>
. b‐AP15 (and presumably VLX1570) are believed to be reversible inhibitors of proteasomal DUBs; nonetheless, they are able to inhibit labeling by irreversible Ub‐VS probes <xref rid="febs14039-bib-0102" ref-type="ref">102</xref>
. It should be noted that reversible and irreversible inhibitors behave quite differently in competitive ABPP experiments: the degree of inhibition by irreversible inhibitors will be sensitive to the time between inhibitor treatment and labeling, while reversible inhibitors will be affected by changes in concentration between inhibitor treatment and labeling. For a detailed discussion of DUB inhibitors and their selectivity, several recent reviews are available <xref rid="febs14039-bib-0103" ref-type="ref">103</xref>
, <xref rid="febs14039-bib-0104" ref-type="ref">104</xref>
, <xref rid="febs14039-bib-0105" ref-type="ref">105</xref>
, <xref rid="febs14039-bib-0106" ref-type="ref">106</xref>
.</p>
</sec>
</sec>
</sec>
<sec id="febs14039-sec-0015"><title>E1, E2, and E3 enzymes</title>
<p>Activity‐based probes for the E1, E2, and E3 enzymes have received much less attention than ABPs for DUBs. It has been suggested that it is more difficult to trap the active E1, E2, and E3 enzymes with electrophiles due to the lower reactivity of the catalytic Cys residue <xref rid="febs14039-bib-0061" ref-type="ref">61</xref>
, but it is difficult to compare the relative reactivity of Cys residues across different enzymes. There are also many fewer E1 and E2 enzymes than DUBs, so there may be less interest in studying the activity of all members of the enzyme class simultaneously. For E3s, only the HECT and RBR ligases have a catalytic Cys residue, and so most E3s cannot be studied using ABPs. Nonetheless, recent ABPs for the Ub conjugation machinery have provided insights that would have been difficult to obtain using more conventional techniques. Furthermore, the entry of E1 inhibitors and E3 antagonists and inhibitors into the clinic provides additional motivation for developing techniques to study the activity of these enzymes.</p>
<sec id="febs14039-sec-0016"><title>E1</title>
<p>Prior to the development of ABPs for E1 enzymes, tools were designed for use in structural studies to capture the covalent intermediates in the E1 reaction mechanism. This closely parallels the use of Ubal to obtain Ub‐bound DUB structures, prior to the development of DUB ABPs. In an elegant study, Olsen <italic>et al</italic>
. developed a SUMO~AMP mimic to trap the tetrahedral intermediate (E1~SUMO~AMP) formed by the catalytic Cys residue (Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
A) <xref rid="febs14039-bib-0107" ref-type="ref">107</xref>
. In this compound, SUMO1‐AVSN, the acyl‐phosphate linkage of SUMO1~AMP is replaced with a vinyl sulfonamide. They also developed an unreactive SUMO~AMP mimic incorporating an unreactive acyl‐sulfamide (SUMO1‐AMSN). Structures of SUMO E1 bound to the two compounds revealed major differences in protein architecture. The initial E1:SUMO‐AMSN complex adopts an ‘open’ conformation, in which the active site is organized for ATP binding and the catalytic Cys is buried and far from the SUMO adenylate. By contrast, the covalent complex E1~SUMO‐AVSN adopts a ‘closed’ conformation with a radically different active site: residues involved in catalyzing the first step have been ‘swapped’ for those required for the transesterification reaction. Therefore, E1 enzymes appear not to have two spatially distinct active sites; rather, the region around the SUMO C terminus and AMP is remodeled after the adenylation reaction in order to catalyze transesterification. These synthetic SUMO adenylate mimics were vital for crystallizing the E1 enzymes in otherwise transient states, illuminating the complex dynamics of these enzymes during catalysis. Similar probes will also react with and inhibit Ub E1 enzymes <xref rid="febs14039-bib-0108" ref-type="ref">108</xref>
.</p>
<fig fig-type="Figure" xml:lang="en" id="febs14039-fig-0004" orientation="portrait" position="float"><label>Figure 4</label>
<caption><p>Activity‐based probes for the Ub conjugation machinery. (A) E1 probes that label the enzyme active site (Ubl~<styled-content style="fixed-case" toggle="no">AMP</styled-content>
shown for comparison): Ubl‐<styled-content style="fixed-case" toggle="no">AVSN</styled-content>
resembles Ubl~<styled-content style="fixed-case" toggle="no">AMP</styled-content>
but reacts with E1 to form a covalent mimic of the E1:Ubl~<styled-content style="fixed-case" toggle="no">AMP</styled-content>
complex; Ubl‐<styled-content style="fixed-case" toggle="no">AMSN</styled-content>
is an unreactive Ubl~<styled-content style="fixed-case" toggle="no">AMP</styled-content>
analog <xref rid="febs14039-bib-0107" ref-type="ref">107</xref>
, <xref rid="febs14039-bib-0108" ref-type="ref">108</xref>
; Ub‐Probe3 reacts in a similar way to Ubl‐<styled-content style="fixed-case" toggle="no">AVSN</styled-content>
, but incorporates an alkyne tag for detection <xref rid="febs14039-bib-0109" ref-type="ref">109</xref>
; (B) an E1 <styled-content style="fixed-case" toggle="no">ABP</styled-content>
,<styled-content style="fixed-case" toggle="no"> ABP</styled-content>
1 <xref rid="febs14039-bib-0041" ref-type="ref">41</xref>
, which labels Ub, and the <styled-content style="fixed-case" toggle="no">NEDD</styled-content>
8 E1 inhibitor <styled-content style="fixed-case" toggle="no">MLN</styled-content>
4924 (pevonedistat) which shares a similar structure and mechanism; (C) transthiolation probes for the E1‐E2 reaction <xref rid="febs14039-bib-0114" ref-type="ref">114</xref>
and the E2‐E3 reaction <xref rid="febs14039-bib-0115" ref-type="ref">115</xref>
; (D) ‘cascading’ <styled-content style="fixed-case" toggle="no">ABP</styled-content>
Ub‐Dha, which can label E1, E2, and some E3 enzymes <xref rid="febs14039-bib-0061" ref-type="ref">61</xref>
.</p>
</caption>
<graphic id="nlm-graphic-9" xlink:href="FEBS-284-1555-g004"></graphic>
</fig>
<p>Despite the utility of SUMO1‐AVSN in trapping the tetrahedral intermediate in the E1~SUMO~AMP complex, it has several drawbacks as a broadly applicable ABP, including lengthy synthesis, a requirement for a fixed, non‐native sequence at the C terminus of the Ubl, and a lack of a label for detection. To overcome these limitations, An and Statsyuk developed an alternative probe design which used a dehydroalanine (Dha) moiety in place of a vinyl sulfone to trap the catalytic Cys, simplifying synthesis and preserving the C‐terminal sequence of the Ubl (‘Ub‐Probe3’, Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
A) <xref rid="febs14039-bib-0109" ref-type="ref">109</xref>
. Additionally, they incorporated an alkyne tag into the adenine moiety for detection. A wide variety of Ubl‐containing probes could be prepared by their method, and they validated the reactivity of Ub‐ and LC3‐containing probes toward the relevant E1 enzymes (UBA1 and ATG7). Unfortunately, a Ub‐containing probe was cleaved by the DUB IsoT (USP5). The reactivity of other Ubl‐containing probes toward ULPs was not investigated, but this may limit their applicability in studies where DUBs/ULPs are present.</p>
<p>In a separate publication, An and Statsyuk reported an ABP for E1 enzymes that labels the substrate (Ub/Ubl) rather than the enzyme <xref rid="febs14039-bib-0041" ref-type="ref">41</xref>
. The probe, referred to as ABP1 (Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
B), takes advantage of the reversibility of the transthiolation step, in which the E1:AMP~Ub complex transfers Ub to the catalytic Cys to form E1~Ub + AMP (Fig. <xref rid="febs14039-fig-0001" ref-type="fig">1</xref>
B). The authors designed an AMP mimic which would react with the E1~Ub complex to form a stable AMP~Ub analog. As both the adenylation and transthiolation steps must have occurred prior to probe reaction, formation of the AMP~Ub analog reports on E1 activity. ABP1 is an analog of pevonedistat (MLN4924), an inhibitor of the NEDD8 E1 enzyme NAE which is currently in clinical trials <xref rid="febs14039-bib-0110" ref-type="ref">110</xref>
(Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
B). ABP1 differs from pevonedistat in showing pan‐E1 reactivity, and additionally includes an alkyne for detection or enrichment (though ‘click’ reactions to fluorophore‐azide or biotin‐azide, respectively). The probe will react with a variety of E1 enzymes <italic>in vitro</italic>
, in the presence of their cognate Ub/Ubl protein and ATP. Significantly, ABP1 is cell‐permeable, and was used to characterize the intracellular potency and selectivity of E1 inhibitors. A close analog of ABP1, ABP3, selectively labeled Ub and NEDD8 over other Ubls, suggesting selectivity toward the Ub and NEDD8 E1 enzymes <xref rid="febs14039-bib-0111" ref-type="ref">111</xref>
. An unexpected advantage of these probes is that the <italic>N</italic>
‐acylsulfamate linker, formed between the Ub/Ubl and the probe, is cleaved under acidic conditions. This facilitates subsequent proteomic studies, as proteins can be eluted under relatively mild conditions after biotin–streptavidin affinity purification, reducing background from nonspecifically bound proteins <xref rid="febs14039-bib-0112" ref-type="ref">112</xref>
, <xref rid="febs14039-bib-0113" ref-type="ref">113</xref>
.</p>
<p>The probes described above are useful for studying the Ub‐activating activity of E1 enzymes. However, E1 enzymes are also involved in a second process, the transfer of Ub to E2 enzymes. Stanley <italic>et al</italic>
. <xref rid="febs14039-bib-0114" ref-type="ref">114</xref>
have developed ABPs to profile this E1‐E2 transthiolation reaction, which consist of an E2 enzyme tagged with a electrophile on the catalytic Cys. These probes undergo a proximity‐dependent reaction with the catalytic Cys of active E1 enzymes (Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
C). A probe derived from the E2 UBE2N selectively labeled the E1 UBA1 in cell lysate, and could be used in a competitive ABPP experiment to test E1 inhibitors. Perhaps surprisingly, E2‐derived probes did not label E3s. The authors suggest that Ub in E2~Ub is required to induce a transthiolation‐competent conformation of the E3. Indeed, the authors have subsequently reported probes containing a Ub moiety as RBR ligase ABPs <xref rid="febs14039-bib-0115" ref-type="ref">115</xref>
, which are discussed below.</p>
</sec>
<sec id="febs14039-sec-0017"><title>E3</title>
<p>Although the majority of E3 ligases do not form a covalent intermediate with Ub, those of the HECT and RBR families accept Ub from E2 enzymes in a transthiolation reaction, and subsequently transfer it to substrates in an aminolysis step. The covalent nature of the intermediate makes the HECT and RBR E3s suitable candidates for the development of ABPs. Only recently have the first ABPs for the transthiolation step been described <xref rid="febs14039-bib-0115" ref-type="ref">115</xref>
, which build on the E2‐derived probes for E1‐E2 transthiolation described above <xref rid="febs14039-bib-0114" ref-type="ref">114</xref>
. In those probes, the E2 active site was modified to trap cognate E1 enzymes, but they did not react with E3s, which additionally require E2‐bound Ub to activate E3 enzymes for transthiolation. Pao <italic>et al</italic>
. extended these probes with a Ub moiety to generate an E2~Ub conjugate with an internal electrophile (Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
C). For ease of detection, the E2 enzyme could be prepared with a His<sub>6</sub>
epitope tag and an alkyne tag, allowing conjugation to a fluorophore for rapid detection of labeled species by in‐gel fluorescence. A UBE2L3‐containing probe labeled the E3 ligase parkin, a member of the RBR family encoded by the <italic>PARK6</italic>
gene, which is mutated in an autosomal‐recessive form of Parkinson's disease (PD). The authors tested the transthiolation activity of recombinant parkin mutants derived from patients with PD, and found that 10 of 12 mutants tested had reduced transthiolation activity. The probes were also used to investigate parkin activation in cells. Mitochondrial depolarization activates the kinase PINK1 (encoded by <italic>PARK6</italic>
), which in turn activates parkin. In cells derived from PD patients with mutations in <italic>PARK2</italic>
or <italic>PARK6</italic>
, chemical induction of mitochondrial depolarization did not activate parkin (as detected by probe labeling), in contrast to the activation observed in wild‐type cells. While the number of samples tested here was small, this observation suggests the possibility of using these probes to diagnose familial forms of PD in which the PINK1/parkin pathway is mutated.</p>
<p>We anticipate that the E3 ligase probes described by Pao <italic>et al</italic>
. will find applications beyond the detailed dissection of a single E2‐E3 interaction. For example, the probes could be used to identify novel E3s that interact with a given E2, or could be used in competitive ABPP experiments to identify inhibitors or activators of E2‐E3 transthiolation. With the increasing sophistication of techniques to produce modified or fusion proteins, and to introduce reactive functionality, we expect that new methods to study E1, E2, and E3 enzymes will emerge over the next few years.</p>
</sec>
<sec id="febs14039-sec-0018"><title>Probes to study multiple members of the Ub conjugation/deconjugation machinery</title>
<p>Deubiquitinase ABPs such as HA‐Ub‐VME cross‐react with E1, E2, and E3 enzymes, and for one HECT E3 ligase, this reaction was shown to occur on Cys residues <xref rid="febs14039-bib-0042" ref-type="ref">42</xref>
. A Ub‐VS probe has been used to infer reactivity of a HECT E3 <xref rid="febs14039-bib-0115" ref-type="ref">115</xref>
, but clearly these probes are not optimized for studying multiple types of enzyme from the UPS simultaneously. Mulder <italic>et al</italic>
. recently published an elegant method to target E1, E2, and E3 enzymes with a single ABP <xref rid="febs14039-bib-0061" ref-type="ref">61</xref>
. The probe, Ub‐Dha (Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
D), can be activated by E1 enzymes in the same manner as Ub and passed sequentially along E2 and E3 enzymes. At each transthiolation step, the probe also has the option of reacting irreversibly with the active site Cys. Importantly, the probe does not become conjugated to target proteins, and appears rather unreactive toward DUBs. The probe could be labeled with a fluorophore or biotin, the latter being used to enrich labeled proteins for proteome‐wide profiling of the Ub conjugation machinery by tandem MS. The authors also delivered the probe to cells by electroporation, potentially overcoming the limitations of performing labeling experiments in lysate, where disruption of intracellular structures and dilution of the cytosol may well reduce the ability of the probe to rapidly label many proteins in the Ub conjugation machinery.</p>
</sec>
</sec>
<sec id="febs14039-sec-0019"><title>Perspective</title>
<p>There now exists an extensive ‘toolbox’ of ABPs for DUBs, and ABPs for E1, E2, and E3 enzymes have recently been reported. Nevertheless, several challenges remain:
<list list-type="bullet" id="febs14039-list-0003"><list-item><p>Cell permeability. Most ABPs for DUBs probes and the Ub conjugation machinery are not cell‐permeable. Studies on the proteasome have shown substantial differences between labeling in lysate and labeling in live cells. Cell‐permeable DUB and E1‐E3 ABPs would open up substantial new opportunities, including the exciting possibility of studying the activity of these enzymes in living organisms. Ward <italic>et al</italic>
. have recently reported a cell‐permeable ABP for USP DUBs by modifying a covalent DUB inhibitor <xref rid="febs14039-bib-0031" ref-type="ref">31</xref>
, and this approach could be extended by attaching reporter tags to other inhibitors <xref rid="febs14039-bib-0104" ref-type="ref">104</xref>
, <xref rid="febs14039-bib-0106" ref-type="ref">106</xref>
.</p>
</list-item>
<list-item><p>Subtype selectivity of DUB probes. Broad‐spectrum DUB probes are extremely useful for ABPP experiments, but more selective probes would be useful to study a single enzyme or small subset of enzymes, for example, when examining the pharmacodynamics of a DUB inhibitor. Substrate‐selective DUB probes are likely to have increased sensitivity, and deconvolution of individual proteins becomes unnecessary. Selective small molecules or engineered Ub variants <xref rid="febs14039-bib-0116" ref-type="ref">116</xref>
, <xref rid="febs14039-bib-0117" ref-type="ref">117</xref>
could provide suitable recognition elements.</p>
</list-item>
<list-item><p>M1‐linked di‐Ub probes. There is an increasing interest in M1‐linked chains and their corresponding deubiquitinases, which have important roles in inflammation <xref rid="febs14039-bib-0118" ref-type="ref">118</xref>
, <xref rid="febs14039-bib-0119" ref-type="ref">119</xref>
. ABPs for M1‐specific DUBs would be valuable tools for studying this physiologically intriguing linkage.</p>
</list-item>
<list-item><p>Probes for JAMM/MPN+ DUBs. The JAMM/MPN+ family DUBs are zinc‐dependent metalloproteases, and so do not form a covalent intermediate with the substrate. It is therefore challenging to develop ABPs that become covalently attached to the enzyme. Several groups have reported strategies to develop ABPs for metalloproteases: Cravatt incorporated a photocrosslinker and alkyne tag into a metal‐chelating inhibitor <xref rid="febs14039-bib-0120" ref-type="ref">120</xref>
, while we have introduced a Cys residue into the protein of interest that could react with an electrophile on the probe <xref rid="febs14039-bib-0121" ref-type="ref">121</xref>
. Similar strategies could be applied to develop covalent ABPs for JAMM/MPN+ DUBs.</p>
</list-item>
<list-item><p>E2 probes. Aside from the ‘cascading’ ABP reported by Mulder <italic>et al</italic>
., there are no ABPs for E2 enzymes. E2‐based probes for the transthiolation activity of E1 and E3 enzymes have been described <xref rid="febs14039-bib-0114" ref-type="ref">114</xref>
, <xref rid="febs14039-bib-0115" ref-type="ref">115</xref>
(Fig. <xref rid="febs14039-fig-0004" ref-type="fig">4</xref>
C), and analogous probes based on E1 or E3 enzymes may be useful to study the transthiolation activity of E2s.</p>
</list-item>
<list-item><p>Effect of post‐translational modification of Ub. Recent studies have shown that Ub can be modified by phosphorylation or acetylation, with significant biological consequences (reviewed in <xref rid="febs14039-bib-0122" ref-type="ref">122</xref>
). However, the mechanisms by which these modifications affect the function of Ub are poorly understood. Synthetic and semisynthetic methods to produce homogeneously modified Ub or Ub chains have been reported <xref rid="febs14039-bib-0029" ref-type="ref">29</xref>
but have not yet been applied to ABPs. Probes for the Ub conjugation or deconjugation machinery incorporating defined modifications could provide insights into how modification of Ub affects its function.</p>
</list-item>
</list>
</p>
<p>Ubiquitination is a versatile process, and correspondingly versatile techniques are required to study it. ABPs, by physically coupling protein to probe in an enzyme‐catalyzed reaction, are especially suited for studying the ubiquitinating and deubiquitinating enzymes. By recognizing what features are shared between enzymes (e.g., nucleophilic Cys residues, a Ub‐binding site close to the catalytic center), and what features differ (e.g., number of Ub‐binding sites), probes have been developed which can interrogate specific components of the ubiquitination/deubiquitination system. New probes will no doubt continue to emerge, inspired both by innovative methods in protein chemistry, and the fascinating biology and clinical importance of ubiquitin modification.</p>
</sec>
</body>
<back><ack id="febs14039-sec-0020"><title>Acknowledgements</title>
<p>We thank Norman Cyr (Department of Pathology, Stanford University) for assistance with figures.</p>
</ack>
<ack id="febs14039-sec-0021"><title>Author contributions</title>
<p>DSH, JAF, MB and IEW discussed and developed the concept of the review and edited the manuscript. DSH wrote the review.</p>
</ack>
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