小分子
计算生物学
分子
药物发现
化学
靶蛋白
生物物理学
鉴定(生物学)
纳米技术
组合化学
生物
生物化学
材料科学
基因
植物
有机化学
作者
Melody Y. Pai,Brett Lomenick,Heejun Hwang,Robert H. Schiestl,William H. McBride,Joseph A. Loo,Jing Huang
标识
DOI:10.1007/978-1-4939-2269-7_22
摘要
Drug affinity responsive target stability (DARTS) is a relatively quick and straightforward approach to identify potential protein targets for small molecules. It relies on the protection against proteolysis conferred on the target protein by interaction with a small molecule. The greatest advantage of this method is being able to use the native small molecule without having to immobilize or modify it (e.g., by incorporation of biotin, fluorescent, radioisotope, or photoaffinity labels). Here we describe in detail the protocol for performing unbiased DARTS with complex protein lysates to identify binding targets of small molecules and for using DARTS-Western blotting to test, screen, or validate potential small-molecule targets. Although the ideas have mainly been developed from studying molecules in areas of biology that are currently of interest to us and our collaborators, the general principles should be applicable to the analysis of all molecules in nature.
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