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Enzymes with noncanonical amino acids
被引:44
|作者:
Zhao, Jingming
[1
]
Burke, Ashleigh J.
[1
]
Green, Anthony P.
[1
]
机构:
[1] Univ Manchester, Manchester Inst Biotechnol, Sch Chem, 131 Princess St, Manchester M1 7DN, Lancs, England
基金:
欧洲研究理事会;
英国工程与自然科学研究理事会;
英国生物技术与生命科学研究理事会;
关键词:
Noncanonical amino acids;
Enzyme design;
Directed evolution;
Genetic code expansion;
ARTIFICIAL METALLOENZYMES;
GENETIC INCORPORATION;
COMPUTATIONAL DESIGN;
DIRECTED EVOLUTION;
PROTEINS;
CATALYSIS;
CYCLOPROPANATION;
PROTEASE;
D O I:
10.1016/j.cbpa.2020.01.006
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Enzyme design and engineering strategies rely almost exclusively on nature's alphabet of twenty canonical amino acids. Recent years have seen the emergence of powerful genetic code expansion methods that allow hundreds of structurally diverse amino acids to be installed into proteins in a site-selective manner. Here, we will highlight how the availability of an expanded alphabet of amino acids has opened new avenues in enzyme engineering research. Genetically encoded noncanonical amino acids have provided new tools to probe complex enzyme mechanisms, improve biocatalyst activity and stability, and most ambitiously to design enzymes with new catalytic mechanisms that would be difficult to access within the constraints of the genetic code. We anticipate that the studies highlighted in this article, coupled with the continuing advancements in genetic code expansion technology, will promote the widespread use of noncanonical amino acids in biocatalysis research in the coming years.
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页码:136 / 144
页数:9
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