小分子
纳米技术
透视图(图形)
计算生物学
核酸
药物发现
蛋白质降解
广谱
计算机科学
组合化学
化学
生化工程
生物
工程类
材料科学
人工智能
生物化学
作者
Xiaowei Huang,Fengbo Wu,Jing Ye,Lian Wang,Xiaoyun Wang,Xiang Li,Gu He
标识
DOI:10.1016/j.apsb.2024.01.010
摘要
Targeted protein degradation (TPD) represented by proteolysis targeting chimeras (PROTACs) marks a significant stride in drug discovery. A plethora of innovative technologies inspired by PROTAC have not only revolutionized the landscape of TPD but have the potential to unlock functionalities beyond degradation. Non-small-molecule-based approaches play an irreplaceable role in this field. A wide variety of agents spanning a broad chemical spectrum, including peptides, nucleic acids, antibodies, and even vaccines, which not only prove instrumental in overcoming the constraints of conventional small molecule entities but also provided rapidly renewing paradigms. Herein we summarize the burgeoning non-small molecule technological platforms inspired by PROTACs, including three major trajectories, to provide insights for the design strategies based on novel paradigms.
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