PROTACs: An Emerging Therapeutic Modality in Precision Medicine

被引:271
|
作者
Nalawansha, Dhanusha A. [1 ]
Crews, Craig M. [1 ,2 ,3 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
[2] Yale Univ, Dept Chem, New Haven, CT 06511 USA
[3] Yale Univ, Dept Pharmacol, New Haven, CT 06511 USA
来源
CELL CHEMICAL BIOLOGY | 2020年 / 27卷 / 08期
关键词
TARGETED PROTEIN-DEGRADATION; E3 UBIQUITIN LIGASE; STRUCTURAL BASIS; SELECTIVE DEGRADATION; MEDIATED DEGRADATION; TRANSCRIPTION FACTOR; RBM39; RECRUITMENT; CHIMERAS PROTACS; SMALL MOLECULES; HIGHLY POTENT;
D O I
10.1016/j.chembiol.2020.07.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Targeted protein degradation (TPD) has emerged as an exciting new era in chemical biology and drug discovery. PROteolysis TArgeting Chimera (PROTAC) technology targets cellular proteins for degradation by co-opting the ubiquitin-proteasome system. Over the last 5 years, numerous studies have expanded our understanding of the unique mode of action and advantages of PROTACs, which has in turn spurred interest in both academia and industry to explore PROTACs as a novel therapeutic strategy. In this review, we first highlight the key advantages of PROTACs and then discuss the spatiotemporal regulation of protein degradation. Next, we explore current chemically tractable E3 ligases focusing on expanding the existing repertoire with novel E3 ligases to uncover the full potential of TPD. Collectively, these studies are guiding the development of the PROTAC technology as it emerges as a new modality in precision medicine.
引用
收藏
页码:998 / 1014
页数:17
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