可药性
计算生物学
药物发现
蛋白质降解
蛋白酶体
生化工程
泛素
生物
纳米技术
化学
工程类
生物化学
基因
材料科学
作者
Yue Zhong,Fanglian Chi,Hanyu Wu,Yunxiao Liu,Zhancheng Xie,Wenlong Huang,Wei Shi,Hai Qian
标识
DOI:10.1016/j.ejmech.2022.114142
摘要
Targeted protein degradation technology has evolved a brand-new therapeutic modality from an innovative drug discovery perspective. Though the classical PROTACs has pioneered the way for protein degraders, certain inherent defects such as poor druggability, uncontrollable catalysis caused off-targets, and limited E3 ubiquitin ligases available constitute obstacles that impede further advances. Recent medicinal chemists have preferred to investigate a type of optimized degraders beyond the classical PROTACs, bypassing such disadvantages to better facilitate targeted protein degradation. In this perspective, we comprehensively spotlighted the emerging approaches and techniques applied to the targeted protein degradation, specifically the PROTACs-derived strategies and other alternatives to realize protein degradation via proteasome or lysosome. Besides, contemporary confronted opportunities as well as challenges were further analyzed, with the aim to guide future discovery of novel protein degraders.
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