Recognition-driven chemical labeling of endogenous proteins in multi-molecular crowding in live cells

被引:36
作者
Amaike, Kazuma [1 ]
Tamura, Tomonori [1 ]
Hamachi, Itaru [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Synthet Chem & Biol Chem, Nishikyo Ku, Kyoto 6158510, Japan
[2] Japan Sci & Technol Agcy, CREST, Chiyoda Ku, 5 Sanbancho, Tokyo 1020075, Japan
基金
日本科学技术振兴机构;
关键词
ACTIVITY-BASED PROBES; DIRECTED TOSYL CHEMISTRY; SMALL-MOLECULE; LIVING CELLS; IN-VIVO; PROTEASE ACTIVITY; DEUBIQUITINATING ENZYME; TARGET IDENTIFICATION; RHODIUM CARBENOIDS; CYSTEINE PROTEASES;
D O I
10.1039/c7cc07177a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Endogenous protein labeling is one of the most invaluable methods for studying the bona fide functions of proteins in live cells. However, multi-molecular crowding conditions, such as those that occur in live cells, hamper the highly selective chemical labeling of a protein of interest (POI). We herein describe how the efficient coupling of molecular recognition with a chemical reaction is crucial for selective protein labeling. Recognition-driven protein labeling is carried out by a synthetic labeling reagent containing a protein (recognition) ligand, a reporter tag, and a reactive moiety. The molecular recognition of a POI can be used to greatly enhance the reaction kinetics and protein selectivity, even under live cell conditions. In this review, we also briefly discuss how such selective chemical labeling of an endogenous protein can have a variety of applications at the interface of chemistry and biology.
引用
收藏
页码:11972 / 11983
页数:12
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