Targeted protein degradation in mammalian cells: A promising avenue toward future

被引:13
|
作者
Zhang, Tianyi [1 ]
Liu, Chuanyang [1 ]
Li, Wenying [1 ]
Kuang, Jingyu [1 ]
Qiu, Xin-yuan [1 ]
Min, Lu [1 ]
Zhu, Lingyun [1 ]
机构
[1] Natl Univ Def Technol, Coll Liberal Arts & Sci, Dept Biol & Chem, Changsha 410073, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
UBIQUITIN-PROTEASOME SYSTEM; BETA-CATENIN; LYSOSOMAL DEGRADATION; IN-VITRO; CYCLIN-E; PROTEOLYSIS; ACTIVATION; RECEPTOR; COMPLEX; PHOSPHORYLATION;
D O I
10.1016/j.csbj.2022.09.038
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
In the eukaryotic cellular milieu, proteins are continuously synthesized and degraded effectively via endogenous protein degradation machineries such as the ubiquitin-proteasome and lysosome pathways. By reengineering and repurposing these natural protein regulatory mechanisms, the targeted protein degradation (TPD) strategies are presenting biologists with powerful tools to manipulate the abundance of proteins of interest directly, precisely, and reversibly at the post-translational level. In recent years, TPD is gaining massive attention and is recognized as a paradigm shift both in basic research, application-oriented synthetic biology, and pioneering clinical work. In this review, we summarize the updated information, especially the engineering efforts and developmental route, of current state-of-the-art TPD technology such as Trim-Away, LYTACs, and AUTACs. Besides, the general design principle, benefits, problems, and opportunities to be addressed were further analyzed, with the aim of providing guidelines for exploration, discovery, and further application of novel TPD tools in the future. (C) 2022 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:5477 / 5489
页数:13
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