Seo Seung-Yong, Corson Timothy W
College of Pharmacy, Gachon University, Incheon, South Korea.
Indiana University School of Medicine, Indianapolis, IN, United States.
Methods Enzymol. 2019;622:347-374. doi: 10.1016/bs.mie.2019.02.028. Epub 2019 Mar 15.
Identification of the protein targets of bioactive small molecules is a routine challenge in chemical biology and phenotype-based drug discovery. Recent years have seen an explosion of approaches to meeting this challenge, but the traditional method of affinity pulldowns remains a practical choice in many contexts. This technique can be used as long as an affinity probe can be synthesized, usually with a crosslinking moiety to enable photo-affinity pulldowns. It can be applied to varied tissue types and can be performed with minimal specialized equipment. Here, we provide our protocol for photo-affinity pulldown experiments, with notes on making this method generally applicable to varied target identification challenges.
鉴定生物活性小分子的蛋白质靶点是化学生物学和基于表型的药物发现中的一项常规挑战。近年来,应对这一挑战的方法激增,但传统的亲和拉下法在许多情况下仍是一种实用的选择。只要能合成亲和探针,通常带有交联部分以实现光亲和拉下,就可以使用该技术。它可应用于各种组织类型,并且只需最少的专业设备即可进行。在这里,我们提供光亲和拉下实验的方案,并就使该方法普遍适用于各种靶点鉴定挑战给出说明。