Homogeneous Oligomeric Ligands Prepared via Radical Polymerization that Recognize and Neutralize a Target Peptide
Abiotic ligands that bind to specific biomolecules have attracted attention as substitutes for biomolecular ligands, such as antibodies and aptamers. Radical polymerization enables the production of robust polymeric ligands from inexpensive functional monomers. However, little has been reported abou...
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description | Abiotic ligands that bind to specific biomolecules have attracted attention as substitutes for biomolecular ligands, such as antibodies and aptamers. Radical polymerization enables the production of robust polymeric ligands from inexpensive functional monomers. However, little has been reported about the production of monodispersed polymeric ligands. Herein, we present homogeneous ligands prepared via radical polymerization that recognize epitope sequences on a target peptide and neutralize the toxicity of the peptide. Taking advantage of controlled radical polymerization and separation, a library of multifunctional oligomers with discrete numbers of functional groups was prepared. Affinity screening revealed that the sequence specificity of the oligomer ligands strongly depended on the number of functional groups. The process reported here will become a general step for the development of abiotic ligands that recognize specific peptide sequences.
Homogeneous oligomeric ligands that recognize epitope sequences on a target peptide and neutralize its toxicity have been prepared via radical polymerization of commercial bulk materials. These synthetic ligands, prepared by controlled radical polymerization, oligomer separation, and affinity screening, are an attractive alternative to biomolecular ligands. |
doi_str_mv | 10.1002/anie.201910558 |
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Homogeneous oligomeric ligands that recognize epitope sequences on a target peptide and neutralize its toxicity have been prepared via radical polymerization of commercial bulk materials. These synthetic ligands, prepared by controlled radical polymerization, oligomer separation, and affinity screening, are an attractive alternative to biomolecular ligands.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201910558</identifier><identifier>PMID: 31691476</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Antibodies ; Aptamers ; Biomolecules ; block copolymers ; combinatorial chemistry ; Epitopes ; Functional groups ; homogeneous oligomer ; Humans ; Ligands ; Monomers ; Oligomers ; Peptides ; Peptides - chemistry ; Polymerization ; synthetic ligand ; Target recognition ; Toxicity</subject><ispartof>Angewandte Chemie International Edition, 2020-01, Vol.59 (2), p.679-683</ispartof><rights>2020 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4108-e12d75371a60c5da0e9aaf51f46b5cb9f164c6b3563b167ef3dfaa44ab5dc6683</citedby><cites>FETCH-LOGICAL-c4108-e12d75371a60c5da0e9aaf51f46b5cb9f164c6b3563b167ef3dfaa44ab5dc6683</cites><orcidid>0000-0001-8590-6079 ; 0000-0001-9628-6979</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fanie.201910558$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fanie.201910558$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31691476$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoshino, Yu</creatorcontrib><creatorcontrib>Taniguchi, Shohei</creatorcontrib><creatorcontrib>Takimoto, Hinata</creatorcontrib><creatorcontrib>Akashi, Sotaro</creatorcontrib><creatorcontrib>Katakami, Sho</creatorcontrib><creatorcontrib>Yonamine, Yusuke</creatorcontrib><creatorcontrib>Miura, Yoshiko</creatorcontrib><title>Homogeneous Oligomeric Ligands Prepared via Radical Polymerization that Recognize and Neutralize a Target Peptide</title><title>Angewandte Chemie International Edition</title><addtitle>Angew Chem Int Ed Engl</addtitle><description>Abiotic ligands that bind to specific biomolecules have attracted attention as substitutes for biomolecular ligands, such as antibodies and aptamers. Radical polymerization enables the production of robust polymeric ligands from inexpensive functional monomers. However, little has been reported about the production of monodispersed polymeric ligands. Herein, we present homogeneous ligands prepared via radical polymerization that recognize epitope sequences on a target peptide and neutralize the toxicity of the peptide. Taking advantage of controlled radical polymerization and separation, a library of multifunctional oligomers with discrete numbers of functional groups was prepared. Affinity screening revealed that the sequence specificity of the oligomer ligands strongly depended on the number of functional groups. The process reported here will become a general step for the development of abiotic ligands that recognize specific peptide sequences.
Homogeneous oligomeric ligands that recognize epitope sequences on a target peptide and neutralize its toxicity have been prepared via radical polymerization of commercial bulk materials. These synthetic ligands, prepared by controlled radical polymerization, oligomer separation, and affinity screening, are an attractive alternative to biomolecular ligands.</description><subject>Antibodies</subject><subject>Aptamers</subject><subject>Biomolecules</subject><subject>block copolymers</subject><subject>combinatorial chemistry</subject><subject>Epitopes</subject><subject>Functional groups</subject><subject>homogeneous oligomer</subject><subject>Humans</subject><subject>Ligands</subject><subject>Monomers</subject><subject>Oligomers</subject><subject>Peptides</subject><subject>Peptides - chemistry</subject><subject>Polymerization</subject><subject>synthetic ligand</subject><subject>Target recognition</subject><subject>Toxicity</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0UFv1DAQBWALgWgpXDkiS1y4ZPHEsZMcq6rQSqt2VZVzNLEnwVUSb-2kaPvr8XZLkbhwsi1982T7MfYRxAqEyL_i5GiVC6hBKFW9YsegcshkWcrXaV9ImZWVgiP2Lsa75KtK6LfsSIKuoSj1Mbu_8KPvaSK_RH49uN6PFJzha9fjZCPfBNpiIMsfHPIbtM7gwDd-2O3ZI87OT3z-iTO_IeP7yT0ST3P8ipY54PB05LcYepr5hrazs_SevelwiPTheT1hP76d355dZOvr75dnp-vMFCCqjCC3pZIloBZGWRRUI3YKukK3yrR1B7owupVKyxZ0SZ20HWJRYKus0bqSJ-zLIXcb_P1CcW5GFw0NAz49tskl5EoJIetEP_9D7_wSpnS7pCSUeV5UIqnVQZngYwzUNdvgRgy7BkSzL6PZl9G8lJEGPj3HLu1I9oX_-f0E6gP45Qba_SeuOb26PP8b_huWKZcy</recordid><startdate>20200107</startdate><enddate>20200107</enddate><creator>Hoshino, Yu</creator><creator>Taniguchi, Shohei</creator><creator>Takimoto, Hinata</creator><creator>Akashi, Sotaro</creator><creator>Katakami, Sho</creator><creator>Yonamine, Yusuke</creator><creator>Miura, Yoshiko</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8590-6079</orcidid><orcidid>https://orcid.org/0000-0001-9628-6979</orcidid></search><sort><creationdate>20200107</creationdate><title>Homogeneous Oligomeric Ligands Prepared via Radical Polymerization that Recognize and Neutralize a Target Peptide</title><author>Hoshino, Yu ; Taniguchi, Shohei ; Takimoto, Hinata ; Akashi, Sotaro ; Katakami, Sho ; Yonamine, Yusuke ; Miura, Yoshiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4108-e12d75371a60c5da0e9aaf51f46b5cb9f164c6b3563b167ef3dfaa44ab5dc6683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antibodies</topic><topic>Aptamers</topic><topic>Biomolecules</topic><topic>block copolymers</topic><topic>combinatorial chemistry</topic><topic>Epitopes</topic><topic>Functional groups</topic><topic>homogeneous oligomer</topic><topic>Humans</topic><topic>Ligands</topic><topic>Monomers</topic><topic>Oligomers</topic><topic>Peptides</topic><topic>Peptides - chemistry</topic><topic>Polymerization</topic><topic>synthetic ligand</topic><topic>Target recognition</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoshino, Yu</creatorcontrib><creatorcontrib>Taniguchi, Shohei</creatorcontrib><creatorcontrib>Takimoto, Hinata</creatorcontrib><creatorcontrib>Akashi, Sotaro</creatorcontrib><creatorcontrib>Katakami, Sho</creatorcontrib><creatorcontrib>Yonamine, Yusuke</creatorcontrib><creatorcontrib>Miura, Yoshiko</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoshino, Yu</au><au>Taniguchi, Shohei</au><au>Takimoto, Hinata</au><au>Akashi, Sotaro</au><au>Katakami, Sho</au><au>Yonamine, Yusuke</au><au>Miura, Yoshiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Homogeneous Oligomeric Ligands Prepared via Radical Polymerization that Recognize and Neutralize a Target Peptide</atitle><jtitle>Angewandte Chemie International Edition</jtitle><addtitle>Angew Chem Int Ed Engl</addtitle><date>2020-01-07</date><risdate>2020</risdate><volume>59</volume><issue>2</issue><spage>679</spage><epage>683</epage><pages>679-683</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><abstract>Abiotic ligands that bind to specific biomolecules have attracted attention as substitutes for biomolecular ligands, such as antibodies and aptamers. Radical polymerization enables the production of robust polymeric ligands from inexpensive functional monomers. However, little has been reported about the production of monodispersed polymeric ligands. Herein, we present homogeneous ligands prepared via radical polymerization that recognize epitope sequences on a target peptide and neutralize the toxicity of the peptide. Taking advantage of controlled radical polymerization and separation, a library of multifunctional oligomers with discrete numbers of functional groups was prepared. Affinity screening revealed that the sequence specificity of the oligomer ligands strongly depended on the number of functional groups. The process reported here will become a general step for the development of abiotic ligands that recognize specific peptide sequences.
Homogeneous oligomeric ligands that recognize epitope sequences on a target peptide and neutralize its toxicity have been prepared via radical polymerization of commercial bulk materials. These synthetic ligands, prepared by controlled radical polymerization, oligomer separation, and affinity screening, are an attractive alternative to biomolecular ligands.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31691476</pmid><doi>10.1002/anie.201910558</doi><tpages>5</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0001-8590-6079</orcidid><orcidid>https://orcid.org/0000-0001-9628-6979</orcidid></addata></record> |
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subjects | Antibodies Aptamers Biomolecules block copolymers combinatorial chemistry Epitopes Functional groups homogeneous oligomer Humans Ligands Monomers Oligomers Peptides Peptides - chemistry Polymerization synthetic ligand Target recognition Toxicity |
title | Homogeneous Oligomeric Ligands Prepared via Radical Polymerization that Recognize and Neutralize a Target Peptide |
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