Modification of proteins using olefin metathesis

被引:29
作者
Messina, Marco S. [1 ,2 ]
Maynard, Heather D. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, 607 Charles E Young Dr East, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Calif NanoSyst Inst, 570 Westwood Plaza, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
RING-CLOSING METATHESIS; CONTROLLED RADICAL POLYMERIZATION; CROSS-METATHESIS; ARTIFICIAL METALLOENZYMES; OPENING POLYMERIZATION; AMINO-ACIDS; PEPTIDES; CYSTEINE; DESIGN; DEHYDROALANINE;
D O I
10.1039/c9qm00494g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Olefin metathesis has revolutionized synthetic approaches to carbon-carbon bond formation. With a rich history beginning in industrial settings through its advancement in academic laboratories leading to new and highly active metathesis catalysts, olefin metathesis has found use in the generation of complex natural products, the cyclization of bioactive materials, and in the polymerization of new and unique polymer architectures. Throughout this review, we will trace the deployment of olefin metathesis-based strategies for the modification of proteins, a process which has been facilitated by the extensive development of stable, isolable, and highly active transition-metal-based metathesis catalysts. We first begin by summarizing early works which detail peptide modification strategies that played a vital role in identifying stable metathesis catalysts. We then delve into protein modification using cross metathesis and finish with recent work on the generation of protein-polymer conjugates through ring-opening metathesis polymerization.
引用
收藏
页码:1040 / 1051
页数:12
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