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 : 000B30Preclinical evaluation of anti-HER2 Affibody molecules site-specifically labeled with 111In using a maleimido derivative of NODAGA.
Auteurs : RBID : pubmed:22172396English descriptors
- KwdEn :
- Acetates (chemistry), Animals, Antibodies, Monoclonal (chemistry), Antibodies, Monoclonal (immunology), Antibodies, Monoclonal (pharmacokinetics), Binding Sites, Cell Line, Tumor, Chelating Agents (chemistry), Heterocyclic Compounds, 1-Ring (chemistry), Humans, Indium Radioisotopes (chemistry), Isotope Labeling (methods), Male, Maleimides (chemistry), Mice, Receptor, erbB-2 (immunology), Recombinant Fusion Proteins (chemistry), Recombinant Fusion Proteins (immunology), Recombinant Fusion Proteins (pharmacokinetics), Substrate Specificity, Sulfhydryl Compounds (chemistry).
- MESH :
- chemical , chemistry : Acetates, Antibodies, Monoclonal, Chelating Agents, Heterocyclic Compounds, 1-Ring, Indium Radioisotopes, Maleimides, Recombinant Fusion Proteins, Sulfhydryl Compounds.
- chemical , immunology : Antibodies, Monoclonal, Receptor, erbB-2, Recombinant Fusion Proteins.
- chemical , pharmacokinetics : Antibodies, Monoclonal, Recombinant Fusion Proteins.
- methods : Isotope Labeling.
- Animals, Binding Sites, Cell Line, Tumor, Humans, Male, Mice, Substrate Specificity.
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
Links toward previous steps (curation, corpus...)
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><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>
</author>
</titleStmt>
<publicationStmt><date when="2012">2012</date>
<idno type="doi">10.1016/j.nucmedbio.2011.10.013</idno>
<idno type="RBID">pubmed:22172396</idno>
<idno type="pmid">22172396</idno>
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<idno type="wicri:Area/Main/Exploration">000B29</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><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>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><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>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Antibodies, Monoclonal</term>
<term>Receptor, erbB-2</term>
<term>Recombinant Fusion Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacokinetics" xml:lang="en"><term>Antibodies, Monoclonal</term>
<term>Recombinant Fusion Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Isotope Labeling</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Binding Sites</term>
<term>Cell Line, Tumor</term>
<term>Humans</term>
<term>Male</term>
<term>Mice</term>
<term>Substrate Specificity</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>
</front>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><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>
</Pagination>
<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>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Altai</LastName>
<ForeName>Mohamed</ForeName>
<Initials>M</Initials>
<Affiliation>Unit of Biomedical Radiation Sciences, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.</Affiliation>
</Author>
<Author ValidYN="Y"><LastName>Perols</LastName>
<ForeName>Anna</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Karlström</LastName>
<ForeName>Amelie Eriksson</ForeName>
<Initials>AE</Initials>
</Author>
<Author ValidYN="Y"><LastName>Sandström</LastName>
<ForeName>Mattias</ForeName>
<Initials>M</Initials>
</Author>
<Author ValidYN="Y"><LastName>Boschetti</LastName>
<ForeName>Frederic</ForeName>
<Initials>F</Initials>
</Author>
<Author ValidYN="Y"><LastName>Orlova</LastName>
<ForeName>Anna</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Tolmachev</LastName>
<ForeName>Vladimir</ForeName>
<Initials>V</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType>Journal Article</PublicationType>
<PublicationType>Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2011</Year>
<Month>12</Month>
<Day>14</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>Nucl Med Biol</MedlineTA>
<NlmUniqueID>9304420</NlmUniqueID>
<ISSNLinking>0969-8051</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>1-(1,3-carboxypropyl)-4,7-carboxymethyl-1,4,7-triazacyclononane</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>Acetates</NameOfSubstance>
</Chemical>
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<NameOfSubstance>Antibodies, Monoclonal</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>Chelating Agents</NameOfSubstance>
</Chemical>
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<NameOfSubstance>Heterocyclic Compounds, 1-Ring</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>Indium Radioisotopes</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>Maleimides</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>Recombinant Fusion Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance>Sulfhydryl Compounds</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>541-59-3</RegistryNumber>
<NameOfSubstance>maleimide</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>EC 2.7.10.1</RegistryNumber>
<NameOfSubstance>Receptor, erbB-2</NameOfSubstance>
</Chemical>
</ChemicalList>
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<QualifierName MajorTopicYN="N">immunology</QualifierName>
<QualifierName MajorTopicYN="N">pharmacokinetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N">Chelating Agents</DescriptorName>
<QualifierName MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Heterocyclic Compounds, 1-Ring</DescriptorName>
<QualifierName MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Indium Radioisotopes</DescriptorName>
<QualifierName MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Isotope Labeling</DescriptorName>
<QualifierName MajorTopicYN="Y">methods</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Maleimides</DescriptorName>
<QualifierName MajorTopicYN="Y">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Mice</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Receptor, erbB-2</DescriptorName>
<QualifierName MajorTopicYN="Y">immunology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Recombinant Fusion Proteins</DescriptorName>
<QualifierName MajorTopicYN="Y">chemistry</QualifierName>
<QualifierName MajorTopicYN="N">immunology</QualifierName>
<QualifierName MajorTopicYN="N">pharmacokinetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Substrate Specificity</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N">Sulfhydryl Compounds</DescriptorName>
<QualifierName MajorTopicYN="N">chemistry</QualifierName>
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