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Preclinical evaluation of anti-HER2 Affibody molecules site-specifically labeled with 111In using a maleimido derivative of NODAGA.

Identifieur interne : 000B29 ( Main/Exploration ); précédent : 000B28; suivant : 000B30

Preclinical evaluation of anti-HER2 Affibody molecules site-specifically labeled with 111In using a maleimido derivative of NODAGA.

Auteurs : RBID : pubmed:22172396

English descriptors

Abstract

Affibody molecules have demonstrated potential for radionuclide molecular imaging. The aim of this study was to synthesize and evaluate a maleimido derivative of the 1,4,7-triazacyclononane-1-glutaric acid-4,7-diacetic acid (NODAGA) for site-specific labeling of anti-HER2 Affibody molecule.

DOI: 10.1016/j.nucmedbio.2011.10.013
PubMed: 22172396

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Le document en format XML

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<title xml:lang="en">Preclinical evaluation of anti-HER2 Affibody molecules site-specifically labeled with 111In using a maleimido derivative of NODAGA.</title>
<author>
<name sortKey="Altai, Mohamed" uniqKey="Altai M">Mohamed Altai</name>
<affiliation wicri:level="1">
<nlm:affiliation>Unit of Biomedical Radiation Sciences, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.</nlm:affiliation>
<country xml:lang="fr">Suède</country>
<wicri:regionArea>Unit of Biomedical Radiation Sciences, Rudbeck Laboratory, Uppsala University, Uppsala</wicri:regionArea>
</affiliation>
</author>
<author>
<name sortKey="Perols, Anna" uniqKey="Perols A">Anna Perols</name>
</author>
<author>
<name sortKey="Karlstr M, Amelie Eriksson" uniqKey="Karlstr M A">Amelie Eriksson Karlström</name>
</author>
<author>
<name sortKey="Sandstr M, Mattias" uniqKey="Sandstr M M">Mattias Sandström</name>
</author>
<author>
<name sortKey="Boschetti, Frederic" uniqKey="Boschetti F">Frederic Boschetti</name>
</author>
<author>
<name sortKey="Orlova, Anna" uniqKey="Orlova A">Anna Orlova</name>
</author>
<author>
<name sortKey="Tolmachev, Vladimir" uniqKey="Tolmachev V">Vladimir Tolmachev</name>
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<term>Acetates (chemistry)</term>
<term>Animals</term>
<term>Antibodies, Monoclonal (chemistry)</term>
<term>Antibodies, Monoclonal (immunology)</term>
<term>Antibodies, Monoclonal (pharmacokinetics)</term>
<term>Binding Sites</term>
<term>Cell Line, Tumor</term>
<term>Chelating Agents (chemistry)</term>
<term>Heterocyclic Compounds, 1-Ring (chemistry)</term>
<term>Humans</term>
<term>Indium Radioisotopes (chemistry)</term>
<term>Isotope Labeling (methods)</term>
<term>Male</term>
<term>Maleimides (chemistry)</term>
<term>Mice</term>
<term>Receptor, erbB-2 (immunology)</term>
<term>Recombinant Fusion Proteins (chemistry)</term>
<term>Recombinant Fusion Proteins (immunology)</term>
<term>Recombinant Fusion Proteins (pharmacokinetics)</term>
<term>Substrate Specificity</term>
<term>Sulfhydryl Compounds (chemistry)</term>
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<term>Acetates</term>
<term>Antibodies, Monoclonal</term>
<term>Chelating Agents</term>
<term>Heterocyclic Compounds, 1-Ring</term>
<term>Indium Radioisotopes</term>
<term>Maleimides</term>
<term>Recombinant Fusion Proteins</term>
<term>Sulfhydryl Compounds</term>
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<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en">
<term>Antibodies, Monoclonal</term>
<term>Receptor, erbB-2</term>
<term>Recombinant Fusion Proteins</term>
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<term>Antibodies, Monoclonal</term>
<term>Recombinant Fusion Proteins</term>
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<term>Isotope Labeling</term>
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<term>Animals</term>
<term>Binding Sites</term>
<term>Cell Line, Tumor</term>
<term>Humans</term>
<term>Male</term>
<term>Mice</term>
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<front>
<div type="abstract" xml:lang="en">Affibody molecules have demonstrated potential for radionuclide molecular imaging. The aim of this study was to synthesize and evaluate a maleimido derivative of the 1,4,7-triazacyclononane-1-glutaric acid-4,7-diacetic acid (NODAGA) for site-specific labeling of anti-HER2 Affibody molecule.</div>
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<PMID Version="1">22172396</PMID>
<DateCreated>
<Year>2012</Year>
<Month>04</Month>
<Day>30</Day>
</DateCreated>
<DateCompleted>
<Year>2012</Year>
<Month>09</Month>
<Day>17</Day>
</DateCompleted>
<DateRevised>
<Year>2012</Year>
<Month>11</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Electronic">1872-9614</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>39</Volume>
<Issue>4</Issue>
<PubDate>
<Year>2012</Year>
<Month>May</Month>
</PubDate>
</JournalIssue>
<Title>Nuclear medicine and biology</Title>
<ISOAbbreviation>Nucl. Med. Biol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Preclinical evaluation of anti-HER2 Affibody molecules site-specifically labeled with 111In using a maleimido derivative of NODAGA.</ArticleTitle>
<Pagination>
<MedlinePgn>518-29</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.nucmedbio.2011.10.013</ELocationID>
<Abstract>
<AbstractText Label="INTRODUCTION" NlmCategory="BACKGROUND">Affibody molecules have demonstrated potential for radionuclide molecular imaging. The aim of this study was to synthesize and evaluate a maleimido derivative of the 1,4,7-triazacyclononane-1-glutaric acid-4,7-diacetic acid (NODAGA) for site-specific labeling of anti-HER2 Affibody molecule.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The maleimidoethylmonoamide NODAGA (MMA-NODAGA) was synthesized and conjugated to Z(HER2:2395) Affibody molecule having a C-terminal cysteine. Labeling efficiency, binding specificity to and cell internalization by HER2-expressing cells of [(111)In-MMA-NODAGA-Cys(61)]-Z(HER2:2395) were studied. Biodistribution of [(111)In-MMA-NODAGA-Cys(61)]-Z(HER2:2395) and [(111)In-MMA-DOTA-Cys(61)]-Z(HER2:2395) was compared in mice.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The affinity of [MMA-NODAGA-Cys(61)]-Z(HER2:2395) binding to HER2 was 67 pM. The (111)In-labeling yield was 99.6%±0.5% after 30 min at 60°C. [(111)In-MMA-NODAGA-Cys(61)]-Z(HER2:2395) bound specifically to HER2-expressing cells in vitro and in vivo. Tumor uptake of [(111)In-MMA-NODAGA-Cys(61)]-Z(HER2:2395) in mice bearing DU-145 xenografts (4.7%±0.8% ID/g) was lower than uptake of [(111)In-MMA-DOTA-Cys(61)]-Z(HER2:2395) (7.5%±1.6% ID/g). However, tumor-to-organ ratios were higher for [(111)In-MMA-NODAGA-Cys(61)]-Z(HER2:2395) due to higher clearance rate from normal tissues.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">MMA-NODAGA is a promising chelator for site-specific labeling of targeting proteins containing unpaired cysteine. Appreciable influence of chelators on targeting properties of Affibody molecules was demonstrated.</AbstractText>
<CopyrightInformation>Copyright © 2012 Elsevier Inc. All rights reserved.</CopyrightInformation>
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<LastName>Altai</LastName>
<ForeName>Mohamed</ForeName>
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<Affiliation>Unit of Biomedical Radiation Sciences, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.</Affiliation>
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<Language>eng</Language>
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<PublicationType>Research Support, Non-U.S. Gov't</PublicationType>
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<ArticleDate DateType="Electronic">
<Year>2011</Year>
<Month>12</Month>
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<Country>United States</Country>
<MedlineTA>Nucl Med Biol</MedlineTA>
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<ISSNLinking>0969-8051</ISSNLinking>
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<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance>1-(1,3-carboxypropyl)-4,7-carboxymethyl-1,4,7-triazacyclononane</NameOfSubstance>
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<RegistryNumber>EC 2.7.10.1</RegistryNumber>
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