小分子
计算生物学
药品
药物发现
计算机科学
药物靶点
化学
机制(生物学)
生物信息学
生物
药理学
生物化学
认识论
哲学
作者
Ying‐Shan Ren,Huilin Li,Xiu‐Hong Piao,Zhiyou Yang,Shumei Wang,Yue‐Wei Ge
标识
DOI:10.1016/j.bcp.2021.114798
摘要
Drug affinity responsive target stability (DARTS) is a novel target discovery approach and is particularly adept at screening small molecule (SM) targets without requiring any structural modifications. The DARTS method is capable of revealing drug-target interactions from cells or tissues by tracking changes in the stability of proteins acting as receptors of bioactive SMs. Due to its simple operation and high efficiency, the DARTS method has been applied to uncover the drug-action mechanism. This review summarized analytical principles, protocols, validation approaches, applications, and challenges involved in the DARTS method. Due to the innate advantages of the DARTS method, it is expected to be a powerful tool to accelerate SM target discovery, especially for bioactive natural products with unknown mechanisms.
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