Recent insights into the development of therapeutics against coronavirus diseases by targeting N protein
Identifieur interne : 001748 ( Pmc/Corpus ); précédent : 001747; suivant : 001749Recent insights into the development of therapeutics against coronavirus diseases by targeting N protein
Auteurs : Chung-Ke Chang ; Shou-Chen Lo ; Yong-Sheng Wang ; Ming-Hon HouSource :
- Drug Discovery Today [ 1359-6446 ] ; 2015.
Abstract
Coronavirus nucleocapsid proteins are appealing drug targets against coronavirus-induced diseases. A variety of compounds targeting the coronavirus nucleocapsid protein have been developed. Many of these compounds show potential antiviral activity.
Url:
DOI: 10.1016/j.drudis.2015.11.015
PubMed: 26691874
PubMed Central: 7108309
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PMC:7108309Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Recent insights into the development of therapeutics against coronavirus diseases by targeting N protein</title><author><name sortKey="Chang, Chung Ke" sort="Chang, Chung Ke" uniqKey="Chang C" first="Chung-Ke" last="Chang">Chung-Ke Chang</name><affiliation><nlm:aff id="aff0005">Institute of Biomedical Sciences, Academia Sinica, Nangang, Taipei 11529, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lo, Shou Chen" sort="Lo, Shou Chen" uniqKey="Lo S" first="Shou-Chen" last="Lo">Shou-Chen Lo</name><affiliation><nlm:aff id="aff0010">Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Wang, Yong Sheng" sort="Wang, Yong Sheng" uniqKey="Wang Y" first="Yong-Sheng" last="Wang">Yong-Sheng Wang</name><affiliation><nlm:aff id="aff0010">Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Hou, Ming Hon" sort="Hou, Ming Hon" uniqKey="Hou M" first="Ming-Hon" last="Hou">Ming-Hon Hou</name><affiliation><nlm:aff id="aff0010">Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation><affiliation><nlm:aff id="aff0015">Biotechnology Center, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">26691874</idno><idno type="pmc">7108309</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108309</idno><idno type="RBID">PMC:7108309</idno><idno type="doi">10.1016/j.drudis.2015.11.015</idno><date when="2015">2015</date><idno type="wicri:Area/Pmc/Corpus">001748</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001748</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Recent insights into the development of therapeutics against coronavirus diseases by targeting N protein</title><author><name sortKey="Chang, Chung Ke" sort="Chang, Chung Ke" uniqKey="Chang C" first="Chung-Ke" last="Chang">Chung-Ke Chang</name><affiliation><nlm:aff id="aff0005">Institute of Biomedical Sciences, Academia Sinica, Nangang, Taipei 11529, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Lo, Shou Chen" sort="Lo, Shou Chen" uniqKey="Lo S" first="Shou-Chen" last="Lo">Shou-Chen Lo</name><affiliation><nlm:aff id="aff0010">Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Wang, Yong Sheng" sort="Wang, Yong Sheng" uniqKey="Wang Y" first="Yong-Sheng" last="Wang">Yong-Sheng Wang</name><affiliation><nlm:aff id="aff0010">Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation></author><author><name sortKey="Hou, Ming Hon" sort="Hou, Ming Hon" uniqKey="Hou M" first="Ming-Hon" last="Hou">Ming-Hon Hou</name><affiliation><nlm:aff id="aff0010">Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation><affiliation><nlm:aff id="aff0015">Biotechnology Center, National Chung Hsing University, Taichung 40227, Taiwan</nlm:aff></affiliation></author></analytic><series><title level="j">Drug Discovery Today</title><idno type="ISSN">1359-6446</idno><idno type="eISSN">1878-5832</idno><imprint><date when="2015">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>Highlights</title><p><list list-type="simple" id="lis0005"><list-item id="lsti0005"><label>•</label><p id="par0005">Coronavirus nucleocapsid proteins are appealing drug targets against coronavirus-induced diseases.</p></list-item><list-item id="lsti0010"><label>•</label><p id="par0010">A variety of compounds targeting the coronavirus nucleocapsid protein have been developed.</p></list-item><list-item id="lsti0015"><label>•</label><p id="par0015">Many of these compounds show potential antiviral activity.</p></list-item></list></p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Cherry, D K" uniqKey="Cherry D">D.K. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Drug Discov Today</journal-id><journal-id journal-id-type="iso-abbrev">Drug Discov. Today</journal-id><journal-title-group><journal-title>Drug Discovery Today</journal-title></journal-title-group><issn pub-type="ppub">1359-6446</issn><issn pub-type="epub">1878-5832</issn><publisher><publisher-name>Elsevier Ltd.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">26691874</article-id><article-id pub-id-type="pmc">7108309</article-id><article-id pub-id-type="publisher-id">S1359-6446(15)00450-X</article-id><article-id pub-id-type="doi">10.1016/j.drudis.2015.11.015</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Recent insights into the development of therapeutics against coronavirus diseases by targeting N protein</article-title></title-group><contrib-group><contrib contrib-type="author" id="aut0005"><name><surname>Chang</surname><given-names>Chung-ke</given-names></name><xref rid="aff0005" ref-type="aff">1</xref></contrib><contrib contrib-type="author" id="aut0010"><name><surname>Lo</surname><given-names>Shou-Chen</given-names></name><xref rid="aff0010" ref-type="aff">2</xref></contrib><contrib contrib-type="author" id="aut0015"><name><surname>Wang</surname><given-names>Yong-Sheng</given-names></name><xref rid="aff0010" ref-type="aff">2</xref></contrib><contrib contrib-type="author" id="aut0020"><name><surname>Hou</surname><given-names>Ming-Hon</given-names></name><email>mhho@dragon.nchu.edu.tw</email><xref rid="aff0010" ref-type="aff">2</xref><xref rid="aff0015" ref-type="aff">3</xref><xref rid="cor0005" ref-type="corresp">⁎</xref></contrib></contrib-group><aff id="aff0005"><label>1</label>Institute of Biomedical Sciences, Academia Sinica, Nangang, Taipei 11529, Taiwan</aff><aff id="aff0010"><label>2</label>Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 40227, Taiwan</aff><aff id="aff0015"><label>3</label>Biotechnology Center, National Chung Hsing University, Taichung 40227, Taiwan</aff><author-notes><corresp id="cor0005"><label>⁎</label><italic>Corresponding author</italic>:. <email>mhho@dragon.nchu.edu.tw</email></corresp></author-notes><pub-date pub-type="pmc-release"><day>12</day><month>12</month><year>2015</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><month>4</month><year>2016</year></pub-date><pub-date pub-type="epub"><day>12</day><month>12</month><year>2015</year></pub-date><volume>21</volume><issue>4</issue><fpage>562</fpage><lpage>572</lpage><permissions><copyright-statement>Copyright © 2015 Elsevier Ltd. All rights reserved.</copyright-statement><copyright-year>2015</copyright-year><copyright-holder>Elsevier Ltd</copyright-holder><license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p></license></permissions><abstract abstract-type="author-highlights" id="abs0005"><title>Highlights</title><p><list list-type="simple" id="lis0005"><list-item id="lsti0005"><label>•</label><p id="par0005">Coronavirus nucleocapsid proteins are appealing drug targets against coronavirus-induced diseases.</p></list-item><list-item id="lsti0010"><label>•</label><p id="par0010">A variety of compounds targeting the coronavirus nucleocapsid protein have been developed.</p></list-item><list-item id="lsti0015"><label>•</label><p id="par0015">Many of these compounds show potential antiviral activity.</p></list-item></list></p></abstract><abstract id="abs0015"><p>The advent of severe acute respiratory syndrome (SARS) in the 21st century and the recent outbreak of Middle-East respiratory syndrome (MERS) highlight the importance of coronaviruses (CoVs) as human pathogens, emphasizing the need for development of novel antiviral strategies to combat acute respiratory infections caused by CoVs. Recent studies suggest that nucleocapsid (N) proteins from coronaviruses and other viruses can be useful antiviral drug targets against viral infections. This review aims to provide readers with a concise survey of the structural features of coronavirus N proteins and how these features provide insights into structure-based development of therapeutics against coronaviruses. We will also present our latest results on MERS-CoV N protein and its potential as an antiviral drug target.</p></abstract><abstract abstract-type="teaser" id="abs0010"><title>Teaser</title><p>Nucleocapsid proteins are essential for coronavirus viability and constitute potential targets for the development of therapeutics against recent coronavirus outbreaks such as SARS and MERS.</p></abstract></article-meta></front><body><sec id="sec0005"><title>Introduction</title><p id="par0020">Upper and lower respiratory infections caused by viruses are very common in temperate climates <xref rid="bib0530" ref-type="bibr">1</xref>, <xref rid="bib0535" ref-type="bibr">2</xref>, and cause rhinitis, pharyngitis, sinusitis, bronchiolitis and pneumonia <xref rid="bib0540" ref-type="bibr">3</xref>, <xref rid="bib0545" ref-type="bibr">4</xref>. Coronaviruses are a large group of RNA viruses with single-stranded RNA genomes that cause 30% of upper and lower respiratory tract infections in humans. Some coronaviruses such as human coronavirus 229E (HCoV-229E), OC43 (HCoV-OC43), HKU1 (HCoV-HKU1) and NL63 (HCoV-NL63) are detected globally and only evoke mild symptoms in most individuals <xref rid="bib0540" ref-type="bibr">3</xref>, <xref rid="bib0545" ref-type="bibr">4</xref>, <xref rid="bib0550" ref-type="bibr">5</xref>, <xref rid="bib0555" ref-type="bibr">6</xref>, <xref rid="bib0560" ref-type="bibr">7</xref>, <xref rid="bib0565" ref-type="bibr">8</xref>, <xref rid="bib0570" ref-type="bibr">9</xref>, <xref rid="bib0575" ref-type="bibr">10</xref>, <xref rid="bib0580" ref-type="bibr">11</xref>, <xref rid="bib0585" ref-type="bibr">12</xref>, <xref rid="bib0590" ref-type="bibr">13</xref>, <xref rid="bib0595" ref-type="bibr">14</xref>, <xref rid="bib0600" ref-type="bibr">15</xref>, <xref rid="bib0605" ref-type="bibr">16</xref>, <xref rid="bib0610" ref-type="bibr">17</xref>, although some individuals can have more-severe illness <xref rid="bib0615" ref-type="bibr">18</xref>, <xref rid="bib0620" ref-type="bibr">19</xref>. However, other human coronaviruses including the severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle-East respiratory syndrome coronavirus (MERS-CoV) can elicit severe symptoms and even death <xref rid="bib0625" ref-type="bibr">20</xref>, <xref rid="bib0630" ref-type="bibr">21</xref>.</p><p id="par0025">Between 2003 and 2004, SARS-CoV caused a worldwide epidemic and had significant impact on the economy of the countries affected by the outbreak. SARS emerged in November 2002 and was widely prevalent in at least 27 countries with 8096 reported cases and a total of 774 deaths up until 31 July 2003 [case-fatality rate (CFR) of 9.5%; <ext-link ext-link-type="uri" xlink:href="http://www.who.int/csr/sars/country/en/" id="intr0015">http://www.who.int/csr/sars/country/en/</ext-link>]. The clinical circumstances are similar among many human coronaviruses, and are particularly urgent in the case of MERS. Since the emergence of MERS in 2012, there have been 1179 laboratory-confirmed cases of infection with MERS-CoV and a total of 442 deaths as of 4 June 2015 (CFR of 37.4%; <ext-link ext-link-type="uri" xlink:href="http://www.who.int/csr/don/04-june-2015-mers-korea/en/" id="intr0020">http://www.who.int/csr/don/04-june-2015-mers-korea/en/</ext-link>). This CFR is higher than most viruses infecting humans. Based on the sequence analysis of the RNA genome, SARS-CoV probably originated from coronaviruses infecting Chinese rhinolophid bats <xref rid="bib0635" ref-type="bibr">22</xref>, <xref rid="bib0640" ref-type="bibr">23</xref>. The origin of MERS-CoV is still unclear, although dromedary camels have been described as an intermediate host for the virus <xref rid="bib0645" ref-type="bibr">24</xref>, <xref rid="bib0650" ref-type="bibr">25</xref>, <xref rid="bib0655" ref-type="bibr">26</xref>. These zoonotic viruses usually have lower surveillance priorities in the public health network, but once they evolve strains capable of crossing the species barrier to infect humans they can easily cause an outbreak. As is true for all coronavirus infections, there is currently no efficacious therapy available for this disease.</p><p id="par0030">The CoV genome consists of positive-sense, single-stranded RNA of approximately 30 kb in length, and it contains several genes encoding several structural and nonstructural proteins that are required for progeny virion production in a conserved linear arrangement <xref rid="bib0660" ref-type="bibr">27</xref>, <xref rid="bib0665" ref-type="bibr">28</xref>. The CoVs have several conserved structural proteins: the matrix (M) protein, the small envelope (E) protein, the trimeric spike (S) glycoprotein and the nucleocapsid (N) protein. Some variants have a third glycoprotein, hemagglutinin-esterase (HE), which is present in lineage A betacoronaviruses. The N protein is located inside the virus particle and is one of the most abundant structural proteins in CoVs. It binds to the viral RNA genome to form a virion core comprising a ribonucleoprotein (RNP) complex that assumes a long helical structure <xref rid="bib0670" ref-type="bibr">29</xref>, <xref rid="bib0675" ref-type="bibr">30</xref>. The RNP is important for maintaining the RNA in an ordered conformation for replication and transcription. The CoV N protein also plays an essential part in viral RNA synthesis <xref rid="bib0680" ref-type="bibr">31</xref>, <xref rid="bib0685" ref-type="bibr">32</xref>, <xref rid="bib0690" ref-type="bibr">33</xref>. In addition to its role in viral processes, the CoV N protein is also involved in the regulation of cellular processes, such as gene transcription, interferon inhibition, actin reorganization, host cell cycle progression and apoptosis <xref rid="bib0695" ref-type="bibr">34</xref>, <xref rid="bib0700" ref-type="bibr">35</xref>, <xref rid="bib0705" ref-type="bibr">36</xref>, <xref rid="bib0710" ref-type="bibr">37</xref>. Moreover, the N protein is an important diagnostic marker and immunodominant antigen in host immune responses <xref rid="bib0715" ref-type="bibr">38</xref>, <xref rid="bib0720" ref-type="bibr">39</xref>, <xref rid="bib0725" ref-type="bibr">40</xref>. Recent studies suggest that N proteins of coronaviruses and other viruses could be useful antiviral drug targets against infections caused by these viruses because they serve many crucial functions during the viral lifecycle <xref rid="bib0730" ref-type="bibr">41</xref>, <xref rid="bib0735" ref-type="bibr">42</xref>, <xref rid="bib0740" ref-type="bibr">43</xref>. This review aims to provide readers with (i) a concise survey of the structural features of coronavirus N proteins, (ii) an explanation of how these features correlate to ribonucleocapsid formation and (iii) insights into structure-based development of therapeutics against coronaviruses by targeting the N protein. We will also present the latest information on current efforts to develop an antiviral therapeutic against MERS-CoV using its N protein as a target.</p></sec><sec id="sec0010"><title>A concise survey of the structural features of coronavirus N proteins</title><p id="par0035">A combination of protein sequence alignment, secondary structure and intrinsic disorder predictions suggests that all CoV N proteins share the same modular organization <xref rid="bib0745" ref-type="bibr">[44]</xref>. Coronavirus N proteins contain three intrinsically disordered regions (IDRs): N-arm, central linker region (LKR) and C-tail, and two structural domains: N-terminal domain (NTD) and C-terminal domain (CTD), where the NTD and CTD are sandwiched between three IDRs (<xref rid="fig0005" ref-type="fig">Fig. 1</xref>a,b). Previous studies have reported that the NTDs of the CoV N proteins are involved in RNA binding, whereas the CTDs are involved in RNA binding and oligomerization <xref rid="bib0750" ref-type="bibr">45</xref>, <xref rid="bib0755" ref-type="bibr">46</xref>, <xref rid="bib0760" ref-type="bibr">47</xref>, <xref rid="bib0765" ref-type="bibr">48</xref>, <xref rid="bib0770" ref-type="bibr">49</xref>, <xref rid="bib0775" ref-type="bibr">50</xref>. All three IDRs of coronaviral N protein can modulate the RNA-binding and oligomerization properties of NTD and CTD, respectively <xref rid="bib0780" ref-type="bibr">[51]</xref>. For example, N-terminal IDR has been implicated in the RNA binding of the N protein. It has also been reported that the LKR and the C-terminal IDR are involved in the oligomerization of the N protein <xref rid="bib0760" ref-type="bibr">[47]</xref>. In addition, the LKR of the N protein with Ser–Arg-rich sequences has also been shown to contain an RNA-binding region and putative phosphorylation sites that might regulate N protein functions <xref rid="bib0785" ref-type="bibr">52</xref>, <xref rid="bib0790" ref-type="bibr">53</xref>, <xref rid="bib0795" ref-type="bibr">54</xref> and N–M interaction. The RNA-binding activity of the LKR also contributes toward RNA chaperone activity, and is involved in template switching under <italic>in vitro</italic> conditions <xref rid="bib0690" ref-type="bibr">[33]</xref>.<fig id="fig0005"><label>Figure 1</label><caption><p><bold>(a)</bold> Domain organization of human coronavirus nucleocapsid protein. MHV: mouse hepatitis virus; IBV: avian infectious bronchitis virus. <bold>(b)</bold> A schematic mechanism of the oligomeric N protein complexed with RNA showing that the N proteins form a tetramer through the interactions between the C-terminal domains and C-terminal tails of the dimer. <bold>(c)</bold> Ribbon representation of HCoV-OC43 N-NTD structure (left). Ribbon representation of HCoV-OC43 N-NTD structure with AMP depicted as a stick structure (middle). Electrostatic surface of the HCoV-OC43 N-NTD–AMP complex (right). Blue denotes positive charge potential, red indicates negative charge potential. <bold>(d)</bold> Detailed stereoview of the interactions at the AMP-binding site. The dotted green lines represent H-bonds. <bold>(e)</bold> Ribbon representation of the SARS-CoV N-C-terminal-domain (CTD) dimer structure.</p></caption><graphic xlink:href="gr1_lrg"></graphic></fig></p><p id="par0040">To clarify the molecular mechanism of RNP formation in CoVs, the structures of truncated fragments of the N protein, including the N-terminal and C-terminal domains, were determined. Previous studies have reported that the N terminus of the N protein provides a scaffold for RNA binding. Structural analysis revealed that the fold and the distribution of the secondary structures of the N-terminal domain of the N protein are essentially conserved across the various CoVs <xref rid="bib0730" ref-type="bibr">41</xref>, <xref rid="bib0800" ref-type="bibr">55</xref>. The core of the structure of CoV N-NTD adopts a unique five-stranded antiparallel β-sheet sandwiched between loops (or short 3<sub>10</sub> helix) with the topology of β4–β2–β3–β1–β5; and the whole structure presents a right-handed fist-shaped structure in which palm and finger are rich in basic residues and the flexible loops are organized around the β-sheet core of the N-terminal domain (<xref rid="fig0005" ref-type="fig">Fig. 1</xref>c). All CoV N-NTDs possess positively charged amino acids on or near the protruding loop; however, in the SARS-CoV, mouse hepatitis virus (MHV) and avian infectious bronchitis virus (IBV) N-NTDs the protruding segment comprises a β-hairpin, whereas a flexible loop predominates in the HCoV-OC43 N-NTD. Based on the surface charge distribution, the protruding loop of the CoV N-NTD containing several positively charged residues, for example, Arg 106, Arg 107 and Arg 117 in HCoV-OC43, were identified to provide a site for binding of the phosphate backbone of RNA through electrostatic interactions <xref rid="bib0800" ref-type="bibr">[55]</xref>. In the central core of MHV N-NTDs, there are two crucial conserved Tyr residues, Tyr 127 and Tyr 129, that are involved in RNA binding and mutations of these residues to alanine can lead to loss of virus replication <xref rid="bib0805" ref-type="bibr">[56]</xref>. By contrast, alanine substitution of Tyr 94 in the IBV N-NTD, which corresponds to Tyr 126 of HCoV-OC43 and Tyr 129 of MHV, led to a significant decrease in its RNA-binding activity and a total loss of infectivity of the viral RNA to Vero cells <xref rid="bib0810" ref-type="bibr">[57]</xref>. The crystal structures of HCoV-OC43 N-NTD complexed with ribonucleoside 5′-monophosphates (AMP, UMP, GMP and CMP) have been reported to identify a distinct ribonucleotide-binding pocket for understanding the molecular interactions that govern CoV N-NTD binding to RNA <xref rid="bib0730" ref-type="bibr">[41]</xref>. The base of ribonucleoside 5′-monophosphates was inserted into a hole in the N-NTD that was almost perpendicular to the phosphate moiety and the phosphate group was bound to a basic and conserved 5′-phosphate-binding site that contained the largest positively charged region on the N-NTD surface (<xref rid="fig0005" ref-type="fig">Fig. 1</xref>c). The detailed interactions between the AMP and HCoV-OC43 N-NTD are shown in <xref rid="fig0005" ref-type="fig">Fig. 1</xref>d. The amino acid composition of this binding site includes Ser 64, Gly 68, Arg 122, Tyr 124, Tyr 126 and Arg 164. The Arg 122, Tyr 124, Tyr 126 and Arg 164 side-chains generate a distinct ribonucleotide-binding pocket and interact with the ribonucleoside 5′-monophosphate via H-bonding, ionic bonding and π–π stacking forces. Tyr 124 is located on the surface of the N protein in the HCoV-OC43 N-NTD and is directly involved in the interactions with the AMP base through π–π stacking. The phenolic hydroxyl group substituent on Tyr 126 forms H-bonds with the sixth amino groups present in the AMP adenine ring. These amino acids are sequentially and structurally conserved in other HCoV N proteins; therefore, they are probably essential for RNA recognition and interaction in all coronavirus N proteins. All featured three additional HCoV-OC43 N-NTD complexes [cytosine monophosphate (CMP), guanosine monophosphate (GMP) and uridine monophosphate (UMP)] are similar to the interaction of the HCoV-OC43 N-NTD–AMP complex.</p><p id="par0045">Self-association of the N protein is a crucial step in virus particle assembly for CoVs. Previous studies have shown that full-length CoV N proteins can form high-order oligomers, and the C-terminal domains of the CoV N proteins mediate the self-association of the protein to form high-order oligomers <xref rid="bib0815" ref-type="bibr">58</xref>, <xref rid="bib0820" ref-type="bibr">59</xref>. The crystal structures of the C-terminal domains of SARS-CoV, MHV and IBV N proteins show a similar stable fold in which the four-stranded β-sheet forms one face and the α-helices form the opposite face, suggesting that the dimerized N protein is the building block for all groups of coronaviruses <xref rid="bib0750" ref-type="bibr">45</xref>, <xref rid="bib0755" ref-type="bibr">46</xref>, <xref rid="bib0770" ref-type="bibr">49</xref>, <xref rid="bib0775" ref-type="bibr">50</xref>, <xref rid="bib0825" ref-type="bibr">60</xref>. The crystal structure of the C-terminal domain shows a tightly intertwined twofold symmetric C-terminal domain dimer, with a β-hairpin from one subunit extending into the cavity of the opposite subunit, which forms an antiparallel β-sheet stabilized through extensive H-bonding across the dimer interface (<xref rid="fig0005" ref-type="fig">Fig. 1</xref>e). The opposite dimerization interface is composed of several helices, where strong hydrophobic interactions involving hydrophobic residues including tryptophan, phenylalanine, leucine and proline were observed. The hydrophobic interactions between the longest helix and the intermolecular β-sheet were also observed to stabilize the dimer conformation further.</p><p id="par0050">The C-tail region of N protein also has an important role in oligomerization <xref rid="bib0815" ref-type="bibr">[58]</xref>. However, owing to its highly disordered sequence, no NMR or crystal structures have been solved to date. Luo <italic>et al.</italic> report that residues 363–382 of the C-tail region from the SARS-CoV N protein are responsible for RNA binding and the C-terminal half of the protein is associated with oligomerization <xref rid="bib0765" ref-type="bibr">[48]</xref>. In the case of HCoV-229E N protein, CTD with an extended C-tail region enhanced higher-order oligomer formation <xref rid="bib0815" ref-type="bibr">[58]</xref>. The C-tail has also been found to participate in the oligomerization of the SARS-CoV N protein <xref rid="bib0765" ref-type="bibr">[48]</xref>, because the removal of 40 amino acid residues from the C terminus apparently decreased the ability of the protein to oligomerize. Previous studies proposed that the H-bonds across the tetramer interface formed by the main chain atoms of the C-tail region stabilize the oligomerization of the CTD of the N protein through domain swapping.</p><p id="par0055">The CTD of the N protein has been shown to lack RNA-binding activity in some cases <xref rid="bib0830" ref-type="bibr">[61]</xref>; however, the presence of the CTD can increase the RNA-binding affinity of the NTD and assist nucleocapsid formation. In SARS-CoV N protein, the CTD has been shown to bind to RNA if it includes an N-terminal charged region which is part of the CTD structure as shown by NMR spectroscopy <xref rid="bib0745" ref-type="bibr">44</xref>, <xref rid="bib0780" ref-type="bibr">51</xref>. These results led us to propose a helical packaging model of CoV RNP, which will be explained in more detail in the following sections.</p></sec><sec id="sec0015"><title>Packaging of the CoV ribonucleocapsid</title><p id="par0060">Coronavirus genomes are generally very large (>20 kb) and their accommodation into virions <100 nm in diameter requires extensive supercoiling of the nucleic acid into a well-packed RNP. Structural studies of the CoV RNP can be traced back to the late 1970s when electron microscopy (EM) studies of coronaviruses found helical entities within the virus particle <xref rid="bib0835" ref-type="bibr">62</xref>, <xref rid="bib0840" ref-type="bibr">63</xref>, <xref rid="bib0845" ref-type="bibr">64</xref>. The observed helical RNPs had coil diameters of 9–16 nm and a hollow interior of 3–4 nm in diameter. Unfortunately, technical limits at the time only yielded a blurry picture of the RNP, and more-detailed information would not be available until 2006. Advances in 2D electron cryomicroscopy (cryo-EM) and single particle image analysis finally enabled Neuman <italic>et al.</italic> to investigate the structural organization of the SARS-CoV at 4 nm resolution <xref rid="bib0850" ref-type="bibr">[65]</xref>. Interestingly, viral RNP is maintained in a spherically packaged form within SARS-CoV, whereas RNP released from disrupted viral particles took the appearance of strands with a diameter of 15 nm. Later studies employing 3D cryoelectron tomography on MHV and transmissible gastroenteritis virus (TGEV) also observed coiled structures and tubular shapes within the virus particle consistent with the formation of a helical RNP <xref rid="bib0855" ref-type="bibr">[66]</xref>. The tomography results showed quasi-circular density profiles of ∼11 nm in diameter enclosing an empty space of ∼4 nm in diameter, in agreement with early EM studies. Neither the 2D cryo-EM nor the 3D cryo-EM tomography studies found consistently ordered structures within the virion, suggesting that the helical RNP is structurally flexible, a characteristic that might be important in the lifecycle of the virus. This flexibility is not unexpected because RNA is known to be dynamic and exists in multiple folded and unfolded states <xref rid="bib0860" ref-type="bibr">[67]</xref>. The interaction between RNA and CoV N protein could involve the structural and intrinsically disordered regions of the CoV N protein through an induced fit process <xref rid="bib0745" ref-type="bibr">44</xref>, <xref rid="bib0780" ref-type="bibr">51</xref>. Because currently there are no data supporting the existence of long-lived N protein oligomers in the absence of nucleic acid, packaging of the CoV RNP most probably employs an RNA-binding coupled-packaging mechanism such as that proposed for MHV <xref rid="bib0865" ref-type="bibr">[68]</xref>.</p><p id="par0065">Although the structure of any CoV RNP at atomic resolution is still lacking, current 3D structural information and biochemical data allowed Chang <italic>et al.</italic> to propose a putative series of molecular events that led to RNP formation <xref rid="bib0760" ref-type="bibr">[47]</xref>. In the model, RNP formation can be initiated by binding of genomic RNA to either the NTD or the CTD, which in turn facilitates binding to other domains through coupled allostery <xref rid="bib0870" ref-type="bibr">[69]</xref>. The model enables multiple initiation sites in parallel. This initial N-protein–RNA binary complex can then grow by either recruiting additional free N protein or by combining with other binary complexes. In the larger oligomer complex the CTD forms a helical core, such as that observed for the SARS-CoV N protein CTD crystal structure, with the RNA wrapping and twisting along a positively charged groove on the outside of the helix <xref rid="bib0755" ref-type="bibr">[46]</xref>. Presumably, the RNA binds to the CTD helix through its phosphate backbone. In addition to the RNA–CTD interaction, the CTD helix is held together by a number of weak protein–protein interactions <xref rid="bib0820" ref-type="bibr">[59]</xref>. The NTD then forms a cap on the outside of the helical CTD–RNA complex through electrostatic interactions between the NTD and the free phosphate groups on the RNA molecule. RNA bases sticking out of the groove intercalate with a set of conserved aromatic residues, further stabilizing the RNP. Two major features are underscored in this model. First, the intrinsically disordered region between the NTD and CTD plays a crucial part in the process by allowing the two structural domains to adapt a wide range of conformations and positions for optimal packing of the RNP complex. Second, RNP formation is driven by electrostatic interactions and a multitude of weak CTD–CTD interactions, consistent with the idea that local weak interactions can assist the formation of globally stable structures in viral capsids <xref rid="bib0875" ref-type="bibr">[70]</xref>. The use of multiple weak interactions to stabilize the RNP would also minimize the formation of kinetic traps and allow greater control over CoV RNP assembly. Interestingly, the RNP structure proposed for SARS-CoV based on the above process would form a helical structure with a diameter of 16 nm and containing a 4 nm diameter hole, consistent with the cryo-EM results.</p><p id="par0070">It should be stated that, although the model proposed by Chang <italic>et al.</italic> generally recapitulates most of the <italic>in vitro</italic> findings in the literature, there is one minor shortcoming: the model does not attempt to explain the role of the RNA packaging signal, which is crucial for <italic>in vivo</italic> initiation of RNP packaging <xref rid="bib0695" ref-type="bibr">34</xref>, <xref rid="bib0880" ref-type="bibr">71</xref>. Rather, according to the model, all RNA sequences should be more or less equivalent, which might be true after RNP formation is initiated <italic>in vivo</italic>. Despite this minor flaw, this model is currently the only one that provides a biophysical working framework for CoV RNP formation.</p></sec><sec id="sec0020"><title>Insights into development of therapeutics against coronaviruses by targeting N protein</title><p id="par0075">Viral nucleocapsid proteins often are multifunctional and have crucial roles in the viral lifecycle. Previous studies have suggested that the N protein could be used as a target for antiviral drug development against viral infections <xref rid="bib0730" ref-type="bibr">41</xref>, <xref rid="bib0735" ref-type="bibr">42</xref>, <xref rid="bib0815" ref-type="bibr">58</xref>, <xref rid="bib0885" ref-type="bibr">72</xref>. For example, the low sequence variation between strains of influenza viruses suggest that N proteins are genetically stable and less prone to develop resistance against putative inhibitors <xref rid="bib0735" ref-type="bibr">42</xref>, <xref rid="bib0885" ref-type="bibr">72</xref>. Although CoV N protein sequences from different strains of the same species also are highly conserved, the same cannot be said when comparing the N protein sequences between different CoV species. This is particularly true when comparing the degree of sequence conservation among CoV N proteins with that of CoV replicase proteins, which include more-traditional drug targets such as proteases, polymerases and helicases. However, targeting the CoV N protein has some advantages. First, there is a wealth of high-resolution structural information about N proteins from various CoV species, which provides researchers with a good starting point for structure-based drug discovery, whereas the structures of most replicase proteins are still unknown. The availability of high-resolution structures is especially important for drug discovery targeting enzymatic activities, because crucial elements for enzyme function might not be detected from primary sequence analyses <xref rid="bib0890" ref-type="bibr">[73]</xref>. Moreover, CoV N proteins share a common modular organization with highly conserved protein structures, which would allow the development of broad-spectrum anticoronavirus drugs. Second, antiviral drug targets that participate in essential oligomeric interactions are less likely to develop drug-resistant variants <xref rid="bib0895" ref-type="bibr">[74]</xref>. Compounds targeting CoV N proteins could also be used in conjunction with compounds that target the CoV replicase proteins to develop ‘cocktail’ therapies.</p><p id="par0080">Two strategies to inhibit oligomeric N protein function have been reported <xref rid="bib0900" ref-type="bibr">[75]</xref>. The first strategy is to develop antiviral agents that target the RNA-binding site, which contains a number of conserved residues, and specifically block the formation of RNP during genome replication. For example, naproxen and its derivatives have been proposed to intercalate into the hydrophobic pocket on the RNA-binding groove of influenza virus N protein and inhibit its RNA-binding ability, resulting in reduced viral replication <xref rid="bib0905" ref-type="bibr">76</xref>, <xref rid="bib0910" ref-type="bibr">77</xref>. Inhibition of RNP formation by several families of compounds targeting the zinc fingers of HIV N protein has also been demonstrated <xref rid="bib0740" ref-type="bibr">[43]</xref>. A second strategy is to hamper normal N protein oligomerization by enhancing or inhibiting the interaction between N protein molecules. Nucleozin and its derivatives obtained by high-throughput methods have been shown to prevent RNP formation in influenza virus by interfering with N protein oligomerization <xref rid="bib0915" ref-type="bibr">78</xref>, <xref rid="bib0920" ref-type="bibr">79</xref>. Similar stratagems can be applied toward development of anticoronaviral agents. In the following sections, we summarize the CoV N-protein-related actions of existing ligands, newly developed chemicals, peptides and polyphenol compounds (<xref rid="tbl0005" ref-type="table">Table 1</xref>). We will also briefly describe developments in coronaviral N protein vaccines.<table-wrap position="float" id="tbl0005"><label>Table 1</label><caption><p>Listing of compounds acting on CoV N proteins.</p></caption><table frame="hsides" rules="groups"><thead><tr><th align="left"><bold>Ligand</bold></th><th align="left"><bold>Classification</bold></th><th align="left"><bold>Target site</bold></th><th align="left"><bold>Function</bold></th><th align="left"><bold>Refs</bold></th></tr></thead><tbody><tr><td align="left"><bold>PJ34</bold></td><td align="left">Chemical</td><td align="left">NTD</td><td align="left">Inhibition of RNA binding</td><td align="left"><xref rid="bib0770" ref-type="bibr">[49]</xref></td></tr><tr><td align="left"><bold>H3</bold></td><td align="left">Chemical</td><td align="left">NTD</td><td align="left">Inhibition of RNA binding</td><td align="left"><xref rid="bib0925" ref-type="bibr">[81]</xref></td></tr><tr><td align="left"><bold>N377–389</bold></td><td align="left">Peptide</td><td align="left">C terminus</td><td align="left">Inhibition of oligomerization</td><td align="left"><xref rid="bib0810" ref-type="bibr">[57]</xref></td></tr><tr><td align="left"><bold>(−)-Catechin gallate</bold></td><td align="left">Polyphenol compound</td><td align="left">ND</td><td align="left">Inhibition of RNA binding</td><td align="left"><xref rid="bib0930" ref-type="bibr">[82]</xref></td></tr><tr><td align="left"><bold>(−)-Gallocatechingallate</bold></td><td align="left">Polyphenol compound</td><td align="left">ND</td><td align="left">Inhibition of RNA binding</td><td align="left"><xref rid="bib0930" ref-type="bibr">[82]</xref></td></tr></tbody></table><table-wrap-foot><fn><p><italic>Abbreviations</italic>: CoV, coronavirus; H3, 6-chloro-7-(2-morpholin-4-yl-ethylamino) quinoxaline-5, 8-dione; ND, not determined; NTD, N-terminal domain; PJ34, <italic>N</italic>-(6-oxo-5,6-dihydrophenanthridin-2-yl)(<italic>N</italic>,<italic>N</italic>-dimethylamino)acetamide hydrochloride.</p></fn></table-wrap-foot></table-wrap></p><sec id="sec0025"><title>The N-terminal domain of coronavirus N protein as an antiviral target</title><p id="par0085">A detailed high-resolution structure of HCoV-OC43 N-NTD in complex with ribonucleotide monophosphate has been reported by Lin <italic>et al.</italic><xref rid="bib1925" ref-type="bibr">[80]</xref>. They identified a unique ribonucleotide-binding pocket in the center of the N-NTD comprising conserved RNA-binding residues including Arg 122, Tyr 124, Tyr 126 and Arg 164. Mutation of these residues resulted in significant decrease of the RNA-binding affinity of the protein and subsequent decrease in viral replication. This led the authors to postulate that the N-terminal RNA-binding domain of a CoV N protein could serve as a target for development of RNA-binding inhibitors that could act as broad-spectrum antiviral drugs. Compounds binding to this site that act as competitive N protein inhibitors could be employed to combat highly pathogenic CoVs. One such compound is <italic>N</italic>-(6-oxo-5,6-dihydrophenanthridin-2-yl)(<italic>N</italic>,<italic>N</italic>-dimethylamino)acetamide hydrochloride (PJ34) (<xref rid="fig0010" ref-type="fig">Fig. 2</xref>a), which we found to inhibit coronavirus replication and have a potent inhibitory effect on the RNA-binding activity of HCoV-OC43N protein. PJ34 has been reported to protect mice against brain ischemia, splanchnic ischemia, reperfusion and lipopolysaccharide (LPS) toxicity in various models of local inflammation. The crystal structure of PJ34 in complex with HCoV-OC43 N-NTD shows that its aromatic core stacks onto Tyr 124 of N-NTD (<xref rid="fig0010" ref-type="fig">Fig. 2</xref>b,c). The aromatic core also contains a number of H-bond-forming moieties that mediate specific interactions with the protein. It also has an attached branching moiety that fits into the ribonucleotide-binding pocket of N-NTD. Interestingly, binding of PJ34 to N-NTD mimics that of AMP to N-NTD, but PJ34 is buried deeper into the hydrophobic pocket of the protein. Compared with AMP, PJ34 binds more closely to the N-terminal loop of N-NTD, and the branched moiety of PJ34 inserts into an interior core of N-NTD. By contrast, PJ34 and AMP interact with Ser 64, Tyr 124 and Tyr 26, indicating that these three residues have important roles in RNA binding. Because the three residues are structurally conserved they are suitable interaction targets for drug screening endeavors against the N protein. Based on careful study of the chemical features and mechanisms of action of AMP and PJ34, we formulated three general guidelines for development of agents targeting CoV N-NTD. First, a polycyclic aromatic core is required to enable π–π stacking with the tyrosine residues in the N-NTD. Second, the aromatic core requires the presence of moieties capable of forming specific H-bond interactions with the N-NTD. Finally, attaching a branched moiety (or moieties) that fits into the ribonucleotide-binding pocket can enhance the affinity and specificity of the compound (<xref rid="fig0010" ref-type="fig">Fig. 2</xref>d). Using these guidelines as a selection tool for virtual screening, a second compound, 6-chloro-7-(2-morpholin-4-yl-ethylamino) quinoxaline-5, 8-dione (H3), was recently identified as a potential antiviral compound (<xref rid="fig0010" ref-type="fig">Fig. 2</xref>e) <xref rid="bib0925" ref-type="bibr">[81]</xref>. H3 was shown to inhibit the RNA-binding activity of HCoV-OC43 N-NTD with higher efficacy than PJ34 <italic>in vitro</italic>. Structural studies showed that, compared with PJ34, H3 adopted a bound conformation more similar to that of bound AMP, which could suggest that the similarity of a compound's bound conformation to that of AMP might influence its inhibitory activity toward CoV N-NTDs.<fig id="fig0010"><label>Figure 2</label><caption><p><bold>(a)</bold> Chemical structure of <italic>N</italic>-(6-oxo-5,6-dihydrophenanthridin-2-yl)(<italic>N</italic>,<italic>N</italic>-dimethylamino)acetamide hydrochloride (PJ34). <bold>(b)</bold> Structural overview of human coronavirus OC43 (HCoV-OC43) N-N-terminal-domain(NTD)–PJ34 complex. A ribbon representation of the HCoV-OC43 N-NTD with PJ34 depicted as a stick model is shown on the left, whereas the electrostatic surface of the HCoV-OC43 N-NTD–PJ34 complex is shown on the right. Blue denotes positive charge potential, red indicates negative charge potential. <bold>(c)</bold> Detailed view of the interactions between PJ34 and HCoV-OC43 N-NTD, with the H-bonds depicted as green dotted lines. <bold>(d)</bold> Three general guidelines for the design of compounds that bind to the nucleotide-binding pocket of CoV N-NTD, deduced from the molecular structures of PJ34 and AMP. <bold>(e)</bold> Chemical structure of 6-chloro-7-(2-morpholin-4-yl-ethylamino) quinoxaline-5, 8-dione (H3) (left) and a detailed view of the interactions between H3 and HCoV-OC43 N-NTD. H-bonds mediated by the side- and main-chain atoms are marked as red and black dotted lines, respectively. Anion-π and stacking interactions are denoted in blue and green dashed lines, respectively. <bold>(f)</bold> Chemical structure of (−)-catechin gallate and (−)-gallocatechin gallate.</p></caption><graphic xlink:href="gr2_lrg"></graphic></fig></p></sec><sec id="sec0030"><title>Inhibition of coronaviral N protein oligomerization by developing competing peptides</title><p id="par0090">The C-terminal tail has been found to participate in the oligomerization of the SARS-CoV N protein because removal of 40 amino acids from the C terminus apparently decreased the ability of the protein to oligomerize <xref rid="bib0765" ref-type="bibr">[48]</xref>. In HCoV-229E, the HCoV-229E N protein CTD lacking 13 amino acids (residues 377–389) from the C-tail impaired higher-order oligomerization <xref rid="bib0815" ref-type="bibr">[58]</xref>. Based on computer-assisted prediction of its secondary structure and experimental CD results, the end of the C-terminal tail of HCoV-229E N protein CTD forms a short β-strand. H-bonds across the tetramer interface formed by the main chain atoms of the short β-strand can stabilize oligomerization of the C-terminal domain of the N protein through domain swapping. Inhibition of viral N protein oligomerization by developing competing peptides and small organic compounds is an attractive therapeutic strategy against viral infection <xref rid="bib0930" ref-type="bibr">82</xref>, <xref rid="bib0935" ref-type="bibr">83</xref>, <xref rid="bib0940" ref-type="bibr">84</xref>. We have shown that an excess of a peptide based on the sequence of the C-terminal tail interfered with oligomerization of the C-terminal domain of HCoV-229E N protein and had an inhibitory effect on the viral titer <xref rid="bib0815" ref-type="bibr">[58]</xref>. These results suggest that small molecules or peptides designed against the oligomer interface could be potential inhibitors of CoV.</p></sec><sec id="sec0035"><title>The inhibition of coronaviral N protein RNA-binding activity by gallate derivatives</title><p id="par0095">Roh reported a novel method for the discovery of inhibitors targeting the CoV N protein by quantum dot (QD)-conjugated oligonucleotides <xref rid="bib0945" ref-type="bibr">[85]</xref>. This novel method provides a facile and sensitive way of screening compounds against RNA/DNA-binding virus proteins, particularly when incorporated into a biochip system. Roh immobilized SARS-CoV N protein onto a glass chip and screened chemical compounds that inhibited RNA-binding activity of the protein. Two polyphenolic compounds, (−)-catechin gallate and (−)-gallocatechin gallate (<xref rid="fig0010" ref-type="fig">Fig. 2</xref>e), showed remarkable inhibitory activity in a concentration-dependent fashion <italic>in vitro</italic>. At a concentration of ∼110 μM (0.05 μg/ml), (−)-catechin gallate and (−)-gallocatechin gallate showed more than 40% inhibition activity on a nanoparticle-based RNA oligonucleotide biochip system. However, their binding mechanism to the CoV N protein is still unclear. Interestingly, the structures of these compounds generally conform to the guidelines presented above. First, one of the benzene rings and the dihydropyran cycle forms a bulky aromatic core that can participate in stacking interactions. Second, the multiple hydroxyl groups on the aromatic core also have the potential to form H-bonds with the residues on N-NTD. Finally, the remaining benzene rings branching out of the aromatic core can interact with the ribonucleotide-binding pocket of N-NTD. The striking agreement between the catechin gallate compounds and our proposed guidelines raises the possibility that their inhibitory activity arises from the interaction between the compounds and N-NTD. More studies will be required to test this possibility. In addition, the efficacy of these compounds in cells or tissue cultures is unknown and remains to be assessed.</p></sec><sec id="sec0040"><title>Coronavirus vaccination via nucleocapsid protein</title><p id="par0100">Coronaviral N protein has been considered a desirable target for DNA or recombinant-protein-mediated vaccination. Because the N protein resides inside the virus particle, it does not elicit neutralizing antibodies so the goal of viral vaccine development using the N protein has focused on how to induce the generation of cytotoxic T lymphocytes (CTLs) capable of destroying infected cells. Zhu <italic>et al.</italic> and Zhao <italic>et al.</italic> introduced SARS-CoV N protein DNA in mice and were able to induce high CTL activity <xref rid="bib0950" ref-type="bibr">86</xref>, <xref rid="bib0955" ref-type="bibr">87</xref>. Expression of SARS-CoV N protein by other viral vectors, such as the vaccine virus Ankara (MVA-NC), measles virus (rMV-N) and baculovirus (vAc-N), were successful at generating potent SARS-CoV-specific humoral and T-cell-mediated immune responses <xref rid="bib0960" ref-type="bibr">88</xref>, <xref rid="bib0965" ref-type="bibr">89</xref>, <xref rid="bib0970" ref-type="bibr">90</xref>. To enhance N-protein-induced CTLs, fusion proteins where the N protein is attached to a known antigen protein, such as lysosome-associated membrane protein and calreticulin, were also tested in mice and generated strong N-protein-specific humoral and cellular immunity <xref rid="bib0975" ref-type="bibr">91</xref>, <xref rid="bib0980" ref-type="bibr">92</xref>. CTL epitopes in the N protein of SARS-CoV have also been mapped and several regions within the N protein induced cellular immune response in the peptide form <xref rid="bib0985" ref-type="bibr">[93]</xref>. However, the generation of N-protein-specific T cells in different mouse strains required different peptide sequences corresponding to different regions of the N protein. Zhao <italic>et al.</italic> and Cheung <italic>et al.</italic> reported that the N protein peptides NP111, NP331, NP351 and NP220 stimulated proliferation of N-protein-specific T cells in C57BL/6, C3H, BALB/c and HLA-A2.1Kb, respectively <xref rid="bib0990" ref-type="bibr">94</xref>, <xref rid="bib0995" ref-type="bibr">95</xref>. A more promising approach is the development of a fusion protein vaccine containing truncated SARS-CoV S and N proteins to generate specific neutralizing antibodies and induce specific CTLs at the same time <xref rid="bib0995" ref-type="bibr">[95]</xref>. The vaccine was shown to have low cross-reactivity to HCoV-229E or HCoV-OC43. Mice immunized with the vaccine were protected from SARS-CoV when challenged with the virus. However, a major stumbling block in the development of an N-protein-based vaccine is the induction of undesired immune responses that can cause immunopathology <xref rid="bib1000" ref-type="bibr">[96]</xref>. Unfortunately, this could be a general feature of the N protein, because N proteins from other nidoviruses were also shown to induce deleterious immune responses <xref rid="bib1005" ref-type="bibr">[97]</xref>. It is debatable at this stage whether the N protein should be included in subunit vaccines, because it could cause adverse effects if the induction of neutralizing antibodies is not strong enough <xref rid="bib1010" ref-type="bibr">[98]</xref>. Provided that researchers ultimately overcome these problems, the challenge to translate laboratory results to real clinical situations still remains.</p></sec></sec><sec id="sec0045"><title>Future perspectives and concluding remarks</title><p id="par0105">There is no doubt that CoVs have joined the ranks of important human pathogens in this century. This is particularly true when we consider that there have already been two major CoV outbreaks in the past 15 years showing severe clinical signs. The emergence of SARS and MERS has made the identification of potential drug targets and development of effective lead compounds against CoVs an urgent task. During the SARS outbreak, many SARS patients were treated with one of many medication combinations, including ribavirin with corticosteroids, interferon (alfacon-1) with corticosteroids or ribavirin with protease inhibitors, with some encouraging outcomes <xref rid="bib1015" ref-type="bibr">99</xref>, <xref rid="bib1020" ref-type="bibr">100</xref>, <xref rid="bib1025" ref-type="bibr">101</xref>. Although a combination of ribavirin and interferon has shown synergistic effects against MERS-CoV under <italic>in vitro</italic> conditions, results from human trials have been inconclusive <xref rid="bib1030" ref-type="bibr">[102]</xref>, and there is still no definitive treatment regimen established for MERS. It is worrying that there is a lack of specialized therapeutics against CoVs. Current experimental compounds developed to treat CoV infections primarily target the 3C-like (3CL) and papain-like (PLP) proteases, and helicase (Nsp13) <xref rid="bib1035" ref-type="bibr">103</xref>, <xref rid="bib1040" ref-type="bibr">104</xref>. However, antiviral inhibitors targeting these enzymes can act nonspecifically on homologous proteins in the cell, causing host cell toxicity and severe side effects. Therefore, new antiviral strategies and targets are needed to combat infections caused by CoV.</p><p id="par0110">The N protein is an appealing target because it serves as the protein building-block of CoV RNPs involved in viral transcription and replication. In addition to the development of antiviral drugs, CoV N proteins have also been used for the development of vaccines against CoV infections. However, it is unknown whether the vaccine could successfully translate to real clinical situations, or whether it would be equally effective against other CoV diseases such as MERS. To facilitate the discovery of agents that specifically block the formation of RNP during MERS-CoV genome replication, we have solved the crystal structure of the MERS-CoV N-NTD (residues 39 to 165) to a resolution of 2.63 Å (<xref rid="fig0015" ref-type="fig">Fig. 3</xref>a) <xref rid="bib1045" ref-type="bibr">[105]</xref>. Similar to the structures of N-NTDs from other coronaviruses, MERS-CoV N-NTD forms a single domain composed of a five-stranded β-sheet core sandwiched between loops (or short 3<sub>10</sub> helix). Owing to the flexibility of the long loop between strands β2 and β3, it was relatively difficult to locate its precise position. Based on the surface charge distribution and superimposition with HCoV-OC43 and SARS-CoV N-NTDs, we identified the ribonucleotide-binding pocket in the MERS-CoV N-NTD which also contained the conserved RNA-binding residues found in other CoV N-NTDs (<xref rid="fig0015" ref-type="fig">Fig. 3</xref>a,b). This pocket could be a validated target for antiviral drugs that interfere with the RNA-binding activity of the MERS-CoV N protein. In addition to the ribonucleotide-binding pocket, several sites comprising conserved residues on the MERS-CoV N-NTD could be potential ligand-binding sites based on the results of drug-binding site prediction (<xref rid="fig0015" ref-type="fig">Fig. 3</xref>c) <xref rid="bib1050" ref-type="bibr">[106]</xref>. Although these sites might not be directly involved in RNA binding, the binding of small molecule compounds to these sites could still interfere with N protein function, for example through allostery, and could be alternative targets for antiviral drug development.<fig id="fig0015"><label>Figure 3</label><caption><p><bold>(a)</bold> Ribbon representation of Middle-East respiratory syndrome coronavirus (MERS-CoV) N-N-terminal-domain (NTD) structure (left). Electrostatic surface of the MERS-CoV N-NTD structure (right). Blue denotes positive charge potential, red indicates negative charge potential. <bold>(b)</bold> Structural superimposition of the conserved residues of MERS-CoV N-NTD (green) involved in RNA binding with N-NTDs from severe acute respiratory syndrome coronavirus (SARS-CoV) (magenta) (PDB code: <ext-link ext-link-type="uri" xlink:href="pdb:2ofz" id="intr0005">2ofz</ext-link>) and human coronavirus OC43 (HCoV-OC43) (cyan) (PDB code: <ext-link ext-link-type="uri" xlink:href="pdb:3v3p" id="intr0010">3v3p</ext-link>). <bold>(c)</bold> Putative drug-binding sites predicted by metaPocket are shown as brown spheres on the MERS-CoV N-NTD structure. <bold>(d)</bold> Front (left) and back (right) views of the modeled dimer structure of MERS-CoV N-C-terminal-domain (CTD). The two red arrows indicate the position of the two pyramidal hydrophobic cores that stabilize the CTD dimer.</p></caption><graphic xlink:href="gr3_lrg"></graphic></fig></p><p id="par0115">Based on SARS-CoV N-CTD crystal structures, we expect that the two β-strands of the β-hairpin in the CTD of MERS-CoV N protein would be located within residues 311–315 and 329–337, respectively (<xref rid="fig0015" ref-type="fig">Fig. 3</xref>d). In addition to the H-bonds across the dimer interface formed by the main chain atoms, hydrophobic interactions involving several hydrophobic residues generate two pyramidal hydrophobic cores in the SARS-CoV N-CTD; these resemble a bow-tie-shaped pocket and stabilize the dimerization of the C-terminal domain of the N protein <xref rid="bib0750" ref-type="bibr">[45]</xref>. We found that the hydrophobic residues contributing to the dimer formation of the SARS-CoV N protein are conserved in MERS-CoV N-CTD. We suggest that the two pyramidal hydrophobic cores in MERS-CoV N-CTD could also participate in stabilizing the dimers of the MERS-CoV N protein. Targeting this hydrophobic pocket seems to be a promising avenue for the development of anti-MERS-CoV drugs.</p><p id="par0120">In summary, finding small-molecule ligands that bind with high affinity to N protein could be a substantial step toward developing effective therapeutic agents for CoV diseases. The fact that the CoV N protein has many conserved sites that are crucial for its correct function bodes well for the future outlook of this approach. By contrast, because one is essentially trying to block physical phenomena (binding to RNA and self-association) instead of chemical reactions, intimate understanding of the biophysical aspects of the protein are essential for this approach to work. In this regard, advances in our knowledge of CoV N protein structure and physical behavior during this century has helped tremendously. 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Commun.</source><volume>71</volume><year>2015</year><fpage>977</fpage><lpage>980</lpage><pub-id pub-id-type="pmid">26249685</pub-id></element-citation></ref><ref id="bib1050"><label>106</label><element-citation publication-type="journal" id="sbref1050"><person-group person-group-type="author"><name><surname>Zhang</surname><given-names>Z.</given-names></name></person-group><article-title>Identification of cavities on protein surface using multiple computational approaches for drug binding site prediction</article-title><source>Bioinformatics</source><volume>27</volume><year>2011</year><fpage>2083</fpage><lpage>2088</lpage><pub-id pub-id-type="pmid">21636590</pub-id></element-citation></ref></ref-list><bio><graphic xlink:href="fx2_lrg"></graphic><p><bold>Ming-Hon Hou</bold> received his PhD in biochemical sciences from National Taiwan University. He did his postdoctoral research at the Academia Sinica and continued his research in drug design and biophysics at the National Chung Hsing University in Taiwan. He is now Professor and Director of the Institute of Genomics and Bioinformatics, National Chung Hsing University, and jointly appointed as Adjunct Faculty of Molecular and Biological Agricultural Sciences program of the International Graduate Program at Academia Sinica. His research interests cover a wide range of structural biology and drug development topics, including protein structure, unusual DNA structures, DNA–drug and protein–drug interactions.</p></bio><bio><graphic xlink:href="fx1_lrg"></graphic><p><bold>Chung-ke Chang</bold> received his PhD from the Department of biological sciences at Carnegie Mellon University, USA. He has published a number of papers on the structural and biophysical aspects of the SARS coronavirus nucleocapsid protein. Trained as a protein NMR spectroscopist, his research interests range from protein structure elucidation, to characterization of macromolecular interactions to metabolomics. He is currently a postdoctoral fellow at the Institute of Biomedical Sciences, Academia Sinica, Taiwan.</p></bio><ack id="ack0005"><title>Acknowledgments</title><p>This work was supported by <funding-source id="gs1">MOST</funding-source> grant 103-2113-M-005-007-MY3 (M-H.H.). We thank Professor Stanley Perlman (University of Iowa) and Professor Tai-Huang Huang (IBS, Academia Sinica) for their contribution of helpful resources that made this research possible.</p></ack></back></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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