蛋白质降解
蛋白酶体
蛋白质水解
泛素连接酶
医学
前列腺癌
癌症
癌症研究
泛素
生物
细胞生物学
内科学
生物化学
基因
酶
作者
Simin Qi,Jinyun Dong,Zhiyuan Xu,Xiangdong Cheng,Weidong Zhang,Jiang‐Jiang Qin
标识
DOI:10.3389/fphar.2021.692574
摘要
Proteolysis targeting chimeric (PROTAC) technology is an effective endogenous protein degradation tool developed in recent years that can ubiquitinate the target proteins through the ubiquitin-proteasome system (UPS) to achieve an effect on tumor growth. A number of literature studies on PROTAC technology have proved an insight into the feasibility of PROTAC technology to degrade target proteins. Additionally, the first oral PROTACs (ARV-110 and ARV-471) have shown encouraging results in clinical trials for prostate and breast cancer treatment, which inspires a greater enthusiasm for PROTAC research. Here we focus on the structures and mechanisms of PROTACs and describe several classes of effective PROTAC degraders based on E3 ligases.
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