Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec, H3A 0B8, Canada.
Chemistry. 2019 Apr 1;25(19):4885-4898. doi: 10.1002/chem.201805004. Epub 2019 Jan 23.
The elucidation of substrate-protein interactions is an important component of the drug development process. Due to the complexity of native cellular environments, elucidating these fundamental biochemical interactions remains challenging. Photoaffinity labeling (PAL) is a versatile technique that can provide insight into ligand-target interactions. By judicious modification of substrates with a photoreactive group, PAL creates a covalent crosslink between a substrate and its biological target following UV-irradiation. Among the commonly employed photoreactive groups, diazirines have emerged as the gold standard. In this Minireview, recent developments in the field of diazirine-based photoaffinity labeling will be discussed, with emphasis being placed on their applications in chemical proteomic studies.
阐明底物-蛋白质相互作用是药物开发过程中的一个重要组成部分。由于天然细胞环境的复杂性,阐明这些基本的生化相互作用仍然具有挑战性。光亲和标记(PAL)是一种通用的技术,可以深入了解配体-靶标相互作用。通过巧妙地用光反应基团修饰底物,PAL 在 UV 照射后在底物与其生物靶标之间形成共价交联。在常用的光反应基团中,重氮化合物已成为金标准。在这篇综述中,将讨论基于重氮化合物的光亲和标记领域的最新进展,重点介绍它们在化学蛋白质组学研究中的应用。