药物发现
行动方式
计算生物学
小分子
蛋白质组
药物开发
化学
计算机科学
纳米技术
生化工程
药品
药理学
生物
生物化学
材料科学
工程类
作者
Gerard Drewes,Stefan Knapp
标识
DOI:10.1016/j.tibtech.2018.06.008
摘要
Chemical probes represent versatile tools to validate disease-modifying targets. However, evaluating the selectivity of chemical probes in complex cellular systems is a major challenge that needs to be addressed to better understand the mode of action of small molecules and the interpretation of their pharmacological effects. Chemoproteomics has emerged as a key technology to characterize the mode of action of pharmacological modulators such as chemical probes and drugs, and these studies have unraveled the cellular targets of many bioactive compounds. Here we review the role of chemical probes for the validation of new therapeutic targets and their characterization by proteome wide affinity- and activity-based chemical proteomics and recently developed label-free technologies.
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