光亲和标记
化学
双吖丙啶
化学生物学
亲和标签
组合化学
熔丝球蛋白
生物化学
硅烷
蛋白质-蛋白质相互作用
计算生物学
生物正交化学
硅烷
血浆蛋白结合
生物物理学
模块化设计
质谱法
靶蛋白
作用机理
鉴定(生物学)
对接(动物)
作者
Annika C. S. Page,Lauren M. Orr,Margot Meyers,Bridget P. Belcher,Theodore G. Coffey,Spencer O. Scholz,Sabine Cismoski,Daniel K. Nomura,F. Dean Toste
标识
DOI:10.1021/acschembio.5c00396
摘要
Deconvolution of the protein targets of hit compounds from phenotypic screens, often conducted in live cells, is critical for understanding mechanism of action and identifying potentially hazardous off-target interactions. While photoaffinity labeling and chemoproteomics are long-established approaches for discovering small-molecule-protein interactions in live cells, there are a relatively small number of photoaffinity labeling strategies that can be applied for chemoproteomic target identification studies. Recently, we reported a novel chemical framework for photoaffinity labeling based on the photo-Brook rearrangement of acyl silanes and demonstrated its ability, when appended to protein-targeting ligands, to label recombinant proteins. Here, we report the application of these probes to live cell photoaffinity workflows, demonstrate their complementarity to current state-of-the-art minimalist diazirine-based photoaffinity probes, and introduce a modular synthetic route to access acyl silane scaffolds with improved labeling properties.
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