Expanding the horizons of targeted protein degradation: A non-small molecule perspective

被引:20
作者
Huang, Xiaowei [1 ,2 ]
Wu, Fengbo [1 ,2 ]
Ye, Jing [1 ,2 ,4 ,5 ]
Wang, Lian [1 ,2 ]
Wang, Xiaoyun [1 ,2 ,4 ,5 ]
Li, Xiang [3 ]
He, Gu [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Pharm, Chengdu 610041, Peoples R China
[2] Sichuan Univ, West China Hosp, Dept Dermatol & Venerol, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Urol, Chengdu 610041, Peoples R China
[4] Sichuan Univ, Clin Inst Inflammat & Immunol, Frontiers Sci Ctr Dis Related Mol Network, Lab Dermatol,West China Hosp, Chengdu 610041, Peoples R China
[5] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Targeted protein degradation; Proteolysis targeting chimera; Endocytosis; Autophagy; Proximity-inducing modality; Post-translational modification; CHAPERONE-MEDIATED AUTOPHAGY; ANTIBODY-BASED PROTACS; RNA-BINDING PROTEINS; ALPHA-SYNUCLEIN; LYSOSOMAL DEGRADATION; SELECTIVE DEGRADATION; STRUCTURAL BASIS; PEPTIDE PROTAC; TELOMERIC DNA; TRANSCRIPTION;
D O I
10.1016/j.apsb.2024.01.010
中图分类号
R9 [药学];
学科分类号
1007 ;
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.
引用
收藏
页码:2402 / 2427
页数:26
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