Chemical Synthesis of Diubiquitin-Based Photoaffinity Probes for Selectively Profiling Ubiquitin-Binding Proteins

被引:42
|
作者
Liang, Jun [1 ,2 ]
Zhang, Lin [4 ]
Tan, Xiang-Long [3 ]
Qi, Yun-Kun [3 ]
Feng, Shan [4 ]
Deng, Haiteng [4 ]
Yan, Yijing [1 ,2 ]
Zheng, Ji-Shen [1 ,2 ]
Liu, Lei [3 ]
Tian, Chang-Lin [1 ,2 ]
机构
[1] Microscale Univ Sci, Hefei Natl Lab Phys Sci, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, Hefei 230026, Peoples R China
[3] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[4] Tsinghua Univ, MOE Key Lab Bioinformat, Tsinghua Peking Joint Ctr Life Sci, Sch Life Sci, Beijing 100084, Peoples R China
关键词
native chemical ligation; photoaffinity labelling; protein modifications; protein synthesis; ubiquitination; PROTEOMICS REVEALS; PEPTIDE HYDRAZIDES; CHAINS; LIGATION; DEGRADATION; IDENTIFICATION; ACTIVATION; PROTEASE; CYSTEINE; DOMAINS;
D O I
10.1002/anie.201611659
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biochemical studies of cellular processes involving polyubiquitin have gained increasing attention. More tools are needed to identify ubiquitin (Ub)-binding proteins. We report diazirine-based photoaffinity probes that can capture Ub-binding proteins in cell lysates, and show that diazirines are preferable to aryl azides as the photo-crosslinking group, since they decrease non-selective capture. Photoaffinity probes containing at least two Ub units were required to effectively capture Ub-binding proteins. Different capture selectivity was observed for probes containing diubiquitin moieties with different types of linkages, thus indicating the potential to develop linkage-dependent probes for selectively profiling Ub-binding proteins under various cellular conditions.
引用
收藏
页码:2744 / 2748
页数:5
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