An activity-based probe developed by a sequential dehydroalanine formation strategy targets HECT E3 ubiquitin ligases

被引:30
|
作者
Xu, Ling [1 ]
Fan, Jian [1 ]
Wang, Yu [2 ]
Zhang, Zhongping [3 ]
Fu, Yao [1 ]
Li, Yi-Ming [2 ]
Shi, Jing [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
[2] Hefei Univ Technol, Sch Food & Biol Engn, Hefei 230009, Anhui, Peoples R China
[3] Chinese Acad Sci, Inst Intelligent Machines, Hefei 230031, Anhui, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CHEMICAL-SYNTHESIS; PROTEINS; FAMILY; LIGATION; INSIGHTS; CYSTEINE; MEMBERS; CANCER; EDD;
D O I
10.1039/c9cc03739j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
E3 ligases play a critical role in ubiquitin (Ub) conjugation cascades, and any aberration in their activity is associated with a number of diseases. Advancement in our knowledge of understanding the roles of HECT E3s requires biochemical tools such as activity-based probes (ABPs). In this study we developed a novel dehydroalanine (Dha)-based E2-Ub ABP using a strategy that is a combination of practical hydrazide-based native chemical ligation and sequential Dha formation. The probe could be used for labeling HECT E3s not only in vitro but also in endogenous cellular contexts. Our easy-to-implement method is expected to be useful for the preparation of Dha based Ub family E2 conjugate ABPs.
引用
收藏
页码:7109 / 7112
页数:4
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