自噬
嵌合体(遗传学)
药物开发
蛋白质降解
计算生物学
靶向给药
药物发现
药品
生物
生物信息学
细胞生物学
药理学
生物化学
细胞凋亡
基因
作者
Chao Zhang,Yongbo Liu,Guangchen Li,Zhouli Yang,Chi Han,Xiuyun Sun,Chunquan Sheng,Ke Ding,Yu Rao
出处
期刊:Science Bulletin
[Elsevier BV]
日期:2024-03-29
卷期号:69 (11): 1776-1797
被引量:18
标识
DOI:10.1016/j.scib.2024.03.056
摘要
Undruggable targets typically refer to a class of therapeutic targets that are difficult to target through conventional methods or have not yet been targeted, but are of great clinical significance. According to statistics, over 80% of disease-related pathogenic proteins cannot be targeted by current conventional treatment methods. In recent years, with the advancement of basic research and new technologies, the development of various new technologies and mechanisms has brought new perspectives to overcome challenging drug targets. Among them, targeted protein degradation technology is a breakthrough drug development strategy for challenging drug targets. This technology can specifically identify target proteins and directly degrade pathogenic target proteins by utilizing the inherent protein degradation pathways within cells. This new form of drug development includes various types such as proteolysis targeting chimera (PROTAC), molecular glue, lysosome-targeting Chimaera (LYTAC), autophagosome-tethering compound (ATTEC), autophagy-targeting chimera (AUTAC), autophagy-targeting chimera (AUTOTAC), degrader-antibody conjugate (DAC). This article systematically summarizes the application of targeted protein degradation technology in the development of degraders for challenging drug targets. Finally, the article looks forward to the future development direction and application prospects of targeted protein degradation technology.
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