药物发现
泛素连接酶
计算生物学
蛋白质降解
雄激素受体
化学
泛素
药品
蛋白酶体
前列腺癌
药理学
药物开发
生物信息学
蛋白质水解
医学
生物
癌症
生物化学
内科学
酶
基因
作者
Shenxin Zeng,Wenhai Huang,Xiaoliang Zheng,Liyan Cheng,Zhimin Zhang,Jian Wang,Zhengrong Shen
标识
DOI:10.1016/j.ejmech.2020.112981
摘要
Proteolysis targeting chimera (PROTAC), hijacking protein of interest (POI) and recruiting E3 ligase for target degradation via the ubiquitin-proteasome pathway, is a novel drug discovery paradigm which has been widely used as biological tools and medicinal molecules with the potential of clinical application value. Currently, ARV-110, an orally small molecule PROTAC was designed to specifically target Androgen receptor (AR), firstly enters clinical phase I trials for the treatment of metastatic castration-resistant prostate cancer, which turns a new avenue for the development of PROTAC. We herein provide a detail summary on the latest one year progress of PROTAC target various proteins and elucidate the advantages of PROTAC technology. Finally, the potential challenges of this vibrant field are also discussed.
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