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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.
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页码:343 / 361
页数:19
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