靶蛋白
配体(生物化学)
小分子
计算生物学
蛋白质配体
化学
蛋白质-蛋白质相互作用
蛋白酶
药品
组合化学
生物物理学
鉴定(生物学)
生物系统
生物
生物化学
受体
酶
药理学
基因
植物
作者
Brett Lomenick,Gwanghyun Jung,James A. Wohlschlegel,Jing Huang
标识
DOI:10.1002/9780470559277.ch110180
摘要
Drug Affinity Responsive Target Stability is a general methodology for identifying and studying protein-ligand interactions. The technique is based on the principle that when a small molecule compound binds to a protein, the interaction stabilizes the target protein's structure such that it becomes protease resistant. DARTS is particularly useful for the initial identification of the protein targets of small molecules, but can also be used to validate potential protein-ligand interactions predicted or identified by other means and to estimate the affinity of interactions. The approach is simple and advantageous because it can be performed using crude cell lysates and other complex protein mixtures (without requiring purified proteins), and uses native, unmodified small molecules. The protocols provided in this article describe the general approach for performing DARTS experiments, which can be easily modified and scaled to fit the criteria and purpose of any individual project.
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