| Literature DB >> 28145610 |
Jun Liang1, Lin Zhang2, Xiang-Long Tan3, Yun-Kun Qi3, Shan Feng2, Haiteng Deng2, Yijing Yan1, Ji-Shen Zheng1, Lei Liu3, Chang-Lin Tian1.
Abstract
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.Entities:
Keywords: native chemical ligation; photoaffinity labelling; protein modifications; protein synthesis; ubiquitination
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Year: 2017 PMID: 28145610 DOI: 10.1002/anie.201611659
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336