Proteins as Initiators of Controlled Radical Polymerization: Grafting-from via ATRP and RAFT

被引:185
作者
Sumerlin, Brent S. [1 ,2 ]
机构
[1] So Methodist Univ, Dept Chem, Dallas, TX 75275 USA
[2] So Methodist Univ, Ctr Drug Discovery Design & Delivery, Dallas, TX 75275 USA
来源
ACS MACRO LETTERS | 2012年 / 1卷 / 01期
基金
美国国家科学基金会;
关键词
FRAGMENTATION CHAIN TRANSFER; ELECTRON-TRANSFER; BLOCK-COPOLYMERS; POLYMERS; DESIGN;
D O I
10.1021/mz200176g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Many recent developments in polymer chemistry have advanced the synthesis of materials in which synthetic polymers are immobilized to biological (macro) molecules to enhance solubility, stability, activity, or therapeutic utility of the biological entity. In particular, the versatility and robust nature of controlled radical polymerization (CRP) has enabled access to a diverse family of new polymer bioconjugates. While nitroxide-mediated, atom transfer radical (ATRP), and reversible addition-fragmentation chain transfer (RAFT) polymerizations have all proven useful for the preparation of well-defined end functional polymers capable of being efficiently conjugated to biological molecules, ATRP and RAFT have proven especially proficient for the synthesis of conjugates by direct polymerization of vinyl monomers from biological components, functionalized contain a group capable of initiating chain growth. This Viewpoint highlights several recent advances that have relied on grafting from by CRP, with particular attention devoted to a recent report that seeks to facilitate the process of grafting-from proteins via ATRP under biologically relevant conditions.
引用
收藏
页码:141 / 145
页数:5
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