Approaches for Conjugating Tailor-Made Polymers to Proteins

被引:7
|
作者
Paeth, Matthew [1 ]
Stapleton, Jacob [1 ]
Dougherty, Melissa L. [1 ]
Fischesser, Henry [1 ]
Shepherd, Jerry [1 ]
McCauley, Matthew [1 ]
Falatach, Rebecca [1 ]
Page, Richard C. [1 ]
Berberich, Jason A. [1 ]
Konkolewicz, Dominik [1 ]
机构
[1] Miami Univ, Oxford, OH 45056 USA
关键词
TRANSFER RADICAL POLYMERIZATION; FRAGMENTATION CHAIN TRANSFER; UNNATURAL AMINO-ACIDS; RAFT POLYMERIZATION; GRAFTING-FROM; FLUOROPHORE LIGASE; LIVING CELLS; ATRP; STABILITY; SITE;
D O I
10.1016/bs.mie.2016.12.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A series of methods are outlined for attaching functional polymers to proteins. Polymers with good control over structure, functionality, and composition can be created using reversible addition-fragmentation chain transfer (RAFT) polymerization. These polymers can be covalently linked to enzymes and proteins using either the "grafting-to" approach, where a preformed polymer is attached to the protein surface, or the "grafting-from" approach, where the polymer is grown from the protein surface. Methods for grafting-to, or attaching the RAFT chain transfer agent to the protein surface outlined include the commonly used carbodiimide/activated ester (EDC/NHS) coupling. Methods are also outlined to graft-from the surface of the protein using RAFT polymerization. Additionally, it is possible to site specifically introduce a reactive azide group to the protein surface using enzymatic ligation as a posttranslational modification. This reactive azide group can be conjugated to an alkyne-containing polymer using highly efficient click chemistry. These robust protocols can produce protein-polymer conjugates with various architectures and functionalities. Methods are also outlined for characterization of the resulting bioconjugates.
引用
收藏
页码:193 / 224
页数:32
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