Site-specific dual encoding and labeling of proteins via genetic code expansion

被引:19
|
作者
Bednar, Riley M. [1 ,2 ]
Karplus, P. Andrew [1 ,2 ]
Mehl, Ryan A. [1 ,2 ]
机构
[1] Oregon State Univ, Dept Biochem & Biophys, 2011 Agr & Life Sci Bldg, Corvallis, OR 97331 USA
[2] Oregon State Univ, GCE4All Res Ctr, 2011 Agr & Life Sci, Corvallis, OR 97331 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
NONCANONICAL AMINO-ACIDS; TRANSFER-RNA SYNTHETASES; RESONANCE ENERGY-TRANSFER; NEAR-COGNATE SUPPRESSION; IN-VITRO; STRUCTURAL BASIS; SYNTHESIZED PROTEINS; GENERAL STRATEGY; LIVE CELLS; SYSTEM;
D O I
10.1016/j.chembiol.2023.03.004
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
The ability to selectively modify proteins at two or more defined locations opens new avenues for manipu-lating, engineering, and studying living systems. As a chemical biology tool for the site-specific encoding of non-canonical amino acids into proteins in vivo , genetic code expansion (GCE) represents a powerful tool to achieve such modifications with minimal disruption to structure and function through a two-step "dual encoding and labeling"(DEAL) process. In this review, we summarize the state of the field of DEAL us-ing GCE. In doing so, we describe the basic principles of GCE-based DEAL, catalog compatible encoding systems and reactions, explore demonstrated and potential applications, highlight emerging paradigms in DEAL methodologies, and propose novel solutions to current limitations.
引用
收藏
页码:343 / 361
页数:19
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