Koo Tin-Yan, Chung Clive Yik-Sham
School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
Department of Pathology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, People's Republic of China.
Methods Mol Biol. 2025;2921:331-344. doi: 10.1007/978-1-0716-4502-4_18.
Activity-based protein profiling (ABPP) has been widely used for proteome-wide cysteine profiling to study functional cysteines in biological systems. ABPP can also be performed in a competitive manner for lead compound discovery and target identification of the lead compound. Recently, we reported a new class of acrylamide-based cysteine probe, NAIA, which has superior cysteine reaction kinetics to capture more functional cysteines. We further established the workflow of using NAIA for cysteine profiling by mass spectrometry (MS)-based ABPP. Here, we describe a step-by-step protocol using NAIA in the MS-based ABPP experiments for profiling functional cysteines in cancer cells/cell lysates and protein target identification of covalent ligands.
基于活性的蛋白质谱分析(ABPP)已被广泛用于全蛋白质组的半胱氨酸谱分析,以研究生物系统中的功能性半胱氨酸。ABPP也可以以竞争性方式进行,用于先导化合物的发现和先导化合物的靶点鉴定。最近,我们报道了一类新型的基于丙烯酰胺的半胱氨酸探针NAIA,它具有优异的半胱氨酸反应动力学,能够捕获更多的功能性半胱氨酸。我们进一步建立了通过基于质谱(MS)的ABPP使用NAIA进行半胱氨酸谱分析的工作流程。在这里,我们描述了在基于MS的ABPP实验中使用NAIA进行癌细胞/细胞裂解物中功能性半胱氨酸谱分析和共价配体蛋白质靶点鉴定的分步方案。