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A General Methodology Toward Drug/Dye Incorporated Living Copolymer−Protein Hybrids: (NIRF Dye-Glucose) Copolymer−Avidin/BSA Conjugates as Prototypes
Azide-terminated poly(tert-butyl acrylate) was synthesized via atom transfer radical polymerization (ATRP). Subsequent deprotection was performed to yield poly(acrylic acid) (PAA) possessing a reactive chain-end. A one-pot sequential amidation of the PAA with the amine derivatives of a near-infrared...
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Published in: | Bioconjugate chemistry 2009-08, Vol.20 (8), p.1595-1601 |
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container_title | Bioconjugate chemistry |
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creator | Shi, Wei Dolai, Sukanta Averick, Saadyah Fernando, Suraj S Saltos, Jose A L’Amoreaux, William Banerjee, Probal Raja, Krishnaswami |
description | Azide-terminated poly(tert-butyl acrylate) was synthesized via atom transfer radical polymerization (ATRP). Subsequent deprotection was performed to yield poly(acrylic acid) (PAA) possessing a reactive chain-end. A one-pot sequential amidation of the PAA with the amine derivatives of a near-infrared fluorescent dye (ADS832WS) and glucose produced NIRF dye-incorporated water-soluble copolymers. End-group modifications were performed to produce alkyne/biotin-terminated copolymers which were further employed to generate dye-incorporated polymer−protein hybrids via the biotin−avidin interaction with avidin or “click” bioconjugation with azide-modified BSA. We have overcome two fundamental limitations in the synthesis of bioconjugates: (a) the basic restriction in the diversity of copolymers which can be synthesized for producing bioconjugates, (b) the limitation in the number of dyes/drug molecules that can be attached per protein molecule. The copolymers possessed enhanced optical properties compared to the dye due to increased solubility in water. Potential utility of these copolymers and conjugates in multiwell plate based assays, cell surface imaging and in vivo animal imaging were explored. |
doi_str_mv | 10.1021/bc900142y |
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Subsequent deprotection was performed to yield poly(acrylic acid) (PAA) possessing a reactive chain-end. A one-pot sequential amidation of the PAA with the amine derivatives of a near-infrared fluorescent dye (ADS832WS) and glucose produced NIRF dye-incorporated water-soluble copolymers. End-group modifications were performed to produce alkyne/biotin-terminated copolymers which were further employed to generate dye-incorporated polymer−protein hybrids via the biotin−avidin interaction with avidin or “click” bioconjugation with azide-modified BSA. We have overcome two fundamental limitations in the synthesis of bioconjugates: (a) the basic restriction in the diversity of copolymers which can be synthesized for producing bioconjugates, (b) the limitation in the number of dyes/drug molecules that can be attached per protein molecule. The copolymers possessed enhanced optical properties compared to the dye due to increased solubility in water. Potential utility of these copolymers and conjugates in multiwell plate based assays, cell surface imaging and in vivo animal imaging were explored.</description><identifier>ISSN: 1043-1802</identifier><identifier>EISSN: 1520-4812</identifier><identifier>DOI: 10.1021/bc900142y</identifier><identifier>PMID: 19588920</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Acrylic Resins - chemical synthesis ; Acrylic Resins - chemistry ; Animals ; Avidin - chemistry ; Azides - chemistry ; Biochemistry ; Biotin - chemistry ; Chemical synthesis ; Copolymers ; Female ; Fluorescent Dyes - chemical synthesis ; Fluorescent Dyes - chemistry ; Glucose - chemistry ; Mice ; Molecular Structure ; Polymerization ; Proteins ; Prototypes ; Retinal Pigment Epithelium - chemistry ; Retinal Pigment Epithelium - cytology ; Serum Albumin, Bovine - chemistry ; Solubility</subject><ispartof>Bioconjugate chemistry, 2009-08, Vol.20 (8), p.1595-1601</ispartof><rights>Copyright © 2009 American Chemical Society</rights><rights>Copyright American Chemical Society Aug 19, 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a341t-8390473857925361f7176b539b5c8a818d7534423125229ee02575f59aed48523</citedby><cites>FETCH-LOGICAL-a341t-8390473857925361f7176b539b5c8a818d7534423125229ee02575f59aed48523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19588920$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Wei</creatorcontrib><creatorcontrib>Dolai, Sukanta</creatorcontrib><creatorcontrib>Averick, Saadyah</creatorcontrib><creatorcontrib>Fernando, Suraj S</creatorcontrib><creatorcontrib>Saltos, Jose A</creatorcontrib><creatorcontrib>L’Amoreaux, William</creatorcontrib><creatorcontrib>Banerjee, Probal</creatorcontrib><creatorcontrib>Raja, Krishnaswami</creatorcontrib><title>A General Methodology Toward Drug/Dye Incorporated Living Copolymer−Protein Hybrids: (NIRF Dye-Glucose) Copolymer−Avidin/BSA Conjugates as Prototypes</title><title>Bioconjugate chemistry</title><addtitle>Bioconjugate Chem</addtitle><description>Azide-terminated poly(tert-butyl acrylate) was synthesized via atom transfer radical polymerization (ATRP). Subsequent deprotection was performed to yield poly(acrylic acid) (PAA) possessing a reactive chain-end. A one-pot sequential amidation of the PAA with the amine derivatives of a near-infrared fluorescent dye (ADS832WS) and glucose produced NIRF dye-incorporated water-soluble copolymers. End-group modifications were performed to produce alkyne/biotin-terminated copolymers which were further employed to generate dye-incorporated polymer−protein hybrids via the biotin−avidin interaction with avidin or “click” bioconjugation with azide-modified BSA. We have overcome two fundamental limitations in the synthesis of bioconjugates: (a) the basic restriction in the diversity of copolymers which can be synthesized for producing bioconjugates, (b) the limitation in the number of dyes/drug molecules that can be attached per protein molecule. The copolymers possessed enhanced optical properties compared to the dye due to increased solubility in water. Potential utility of these copolymers and conjugates in multiwell plate based assays, cell surface imaging and in vivo animal imaging were explored.</description><subject>Acrylic Resins - chemical synthesis</subject><subject>Acrylic Resins - chemistry</subject><subject>Animals</subject><subject>Avidin - chemistry</subject><subject>Azides - chemistry</subject><subject>Biochemistry</subject><subject>Biotin - chemistry</subject><subject>Chemical synthesis</subject><subject>Copolymers</subject><subject>Female</subject><subject>Fluorescent Dyes - chemical synthesis</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Glucose - chemistry</subject><subject>Mice</subject><subject>Molecular Structure</subject><subject>Polymerization</subject><subject>Proteins</subject><subject>Prototypes</subject><subject>Retinal Pigment Epithelium - chemistry</subject><subject>Retinal Pigment Epithelium - cytology</subject><subject>Serum Albumin, Bovine - chemistry</subject><subject>Solubility</subject><issn>1043-1802</issn><issn>1520-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNplkc1u00AQx1cVqF9w4AXQCgmVHkx29iPe5RbSNo0UWgTlbK3tSXDkeM2uXeQ36Lm3vh5PwlaJqIDTjEa_-c1If0JeAXsPjMMoLwxjIPmwRw5BcZZIDfxZ7JkUCWjGD8hRCGvGmAHN98kBGKW14eyQPEzoDBv0tqafsPvuSle71UBv3E_rS3rm-9XobEA6bwrnW-dthyVdVLdVs6JT17p62KD_dXf_2bsOq4ZeDrmvyvCBvruaf7mgcTWZ1X3hAp7-xU9uq7JqRh-_TuK4WferKA7UBvooct3QYnhBni9tHfDlrh6TbxfnN9PLZHE9m08ni8QKCV2ihWEyFVqlhisxhmUK6ThXwuSq0FaDLlMlpOQCuOLcIDKuUrVUxmIpteLimJxsva13P3oMXbapQoF1bRt0fcg0BzCSMxHJN_-Qa9f7Jj6XcRiDNiLVETrdQoV3IXhcZq2vNtYPGbDsMa3sT1qRfb0T9vkGyydyF08E3m4BW4SnY_-LfgMgBJvL</recordid><startdate>20090819</startdate><enddate>20090819</enddate><creator>Shi, Wei</creator><creator>Dolai, Sukanta</creator><creator>Averick, Saadyah</creator><creator>Fernando, Suraj S</creator><creator>Saltos, Jose A</creator><creator>L’Amoreaux, William</creator><creator>Banerjee, Probal</creator><creator>Raja, Krishnaswami</creator><general>American Chemical Society</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>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20090819</creationdate><title>A General Methodology Toward Drug/Dye Incorporated Living Copolymer−Protein Hybrids: (NIRF Dye-Glucose) Copolymer−Avidin/BSA Conjugates as Prototypes</title><author>Shi, Wei ; 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Subsequent deprotection was performed to yield poly(acrylic acid) (PAA) possessing a reactive chain-end. A one-pot sequential amidation of the PAA with the amine derivatives of a near-infrared fluorescent dye (ADS832WS) and glucose produced NIRF dye-incorporated water-soluble copolymers. End-group modifications were performed to produce alkyne/biotin-terminated copolymers which were further employed to generate dye-incorporated polymer−protein hybrids via the biotin−avidin interaction with avidin or “click” bioconjugation with azide-modified BSA. We have overcome two fundamental limitations in the synthesis of bioconjugates: (a) the basic restriction in the diversity of copolymers which can be synthesized for producing bioconjugates, (b) the limitation in the number of dyes/drug molecules that can be attached per protein molecule. The copolymers possessed enhanced optical properties compared to the dye due to increased solubility in water. 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subjects | Acrylic Resins - chemical synthesis Acrylic Resins - chemistry Animals Avidin - chemistry Azides - chemistry Biochemistry Biotin - chemistry Chemical synthesis Copolymers Female Fluorescent Dyes - chemical synthesis Fluorescent Dyes - chemistry Glucose - chemistry Mice Molecular Structure Polymerization Proteins Prototypes Retinal Pigment Epithelium - chemistry Retinal Pigment Epithelium - cytology Serum Albumin, Bovine - chemistry Solubility |
title | A General Methodology Toward Drug/Dye Incorporated Living Copolymer−Protein Hybrids: (NIRF Dye-Glucose) Copolymer−Avidin/BSA Conjugates as Prototypes |
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