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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.
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页码:7109 / 7112
页数:4
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