反褶积
药物靶点
鉴定(生物学)
计算生物学
计算机科学
药物发现
化学
生化工程
纳米技术
生物系统
生物
生物化学
材料科学
工程类
算法
植物
作者
Yihui Gao,Mingzhe Ma,Wenyang Li,Xiaoguang Lei
标识
DOI:10.1002/advs.202305608
摘要
Abstract As a vital project of forward chemical genetic research, target deconvolution aims to identify the molecular targets of an active hit compound. Chemoproteomics, either with chemical probe‐facilitated target enrichment or probe‐free, provides a straightforward and effective approach to profile the target landscape and unravel the mechanisms of action. Canonical methods rely on chemical probes to enable target engagement, enrichment, and identification, whereas click chemistry and photoaffinity labeling techniques improve the efficiency, sensitivity, and spatial accuracy of target recognition. In comparison, recently developed probe‐free methods detect protein‐ligand interactions without the need to modify the ligand molecule. This review provides a comprehensive overview of different approaches and recent advancements for target identification and highlights the significance of chemoproteomics in investigating biological processes and advancing drug discovery processes.
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