蛋白质水解
泛素连接酶
蛋白酶体
泛素
机制(生物学)
小分子
细胞生物学
蛋白质降解
计算生物学
化学
生物
生物化学
酶
哲学
认识论
基因
作者
Wenhai Huang,Beibei Wang,Zhimin Zhang,Chixiao Zhang,Shenxin Zeng,Zhengrong Shen
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2019-10-01
卷期号:11 (20): 2715-2734
被引量:8
标识
DOI:10.4155/fmc-2019-0161
摘要
Proteolysis-targeting chimeras (PROTACs) have received much attention for their promising therapeutic intervention in recent years. These molecules, with the mechanism of simultaneous recruitment of target protein and an E3 ligase, can trigger the cellular ubiquitin–proteasome system to degrade the target proteins. This article systematically introduces the mechanism of small-molecule PROTACs, and summarized the research progress of small-molecule PROTACs. The prospect for further application and the problems to be solved are also discussed.
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