Noncanonical Amino Acids in Biocatalysis

被引:31
作者
Birch-Price, Zachary [1 ]
Hardy, Florence J. [1 ]
Lister, Thomas M. [1 ]
Kohn, Anna R. [1 ]
Green, Anthony P. [1 ]
机构
[1] Univ Manchester, Manchester Inst Biotechnol, Sch Chem, Manchester M1 7DN, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会; 英国生物技术与生命科学研究理事会;
关键词
TRANSFER-RNA SYNTHETASE; SITE-SPECIFIC INCORPORATION; NUCLEAR-MAGNETIC-RESONANCE; PHOTO-CROSS-LINKING; IN-VIVO INCORPORATION; COLI RIBONUCLEOTIDE REDUCTASE; RADICAL PROPAGATION PATHWAY; ELECTRON-TRANSFER REACTIONS; PROXIMAL HEME LIGAND; ANTARCTICA LIPASE-B;
D O I
10.1021/acs.chemrev.4c00120
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In recent years, powerful genetic code reprogramming methods have emerged that allow new functional components to be embedded into proteins as noncanonical amino acid (ncAA) side chains. In this review, we will illustrate how the availability of an expanded set of amino acid building blocks has opened a wealth of new opportunities in enzymology and biocatalysis research. Genetic code reprogramming has provided new insights into enzyme mechanisms by allowing introduction of new spectroscopic probes and the targeted replacement of individual atoms or functional groups. NcAAs have also been used to develop engineered biocatalysts with improved activity, selectivity, and stability, as well as enzymes with artificial regulatory elements that are responsive to external stimuli. Perhaps most ambitiously, the combination of genetic code reprogramming and laboratory evolution has given rise to new classes of enzymes that use ncAAs as key catalytic elements. With the framework for developing ncAA-containing biocatalysts now firmly established, we are optimistic that genetic code reprogramming will become a progressively more powerful tool in the armory of enzyme designers and engineers in the coming years.
引用
收藏
页码:8740 / 8786
页数:47
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