Genetically-encoded degraders as versatile modulators of intracellular therapeutic targets

IF 4.7 3区 工程技术 Q2 ENGINEERING, BIOMEDICAL
Chuan Dai , Jinpeng Wang , Licheng Tu , Zhuoheng Pan , Jinru Yang , Shuang Zhou , Qinhong Luo , Lizhi Zhu , Yuxin Ye
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引用次数: 0

Abstract

Targeted protein degradation (TPD) is an emerging therapeutic approach that has attracted significant interest. The traditional TPD degraders rely on small molecules that can only target proteins of interest (POI) with known small-molecule binders or appropriate binding pockets. Recently, several genetic-encoded TPD (GE-TPD) strategies have been developed in which the degrader molecules are expressed in cells based on genetic information. GE-TPD discovers POI binders through techniques such as yeast and phage display and expands the E3 ligase toolbox through genetic encoding. In this review, we assess the progress of GE-TPD technologies in recent years and highlight innovative technologies that have the potential to advance the development of GE-TPD.

基因编码降解物作为细胞内治疗靶点的通用调节剂
靶向蛋白降解(TPD)是一种新兴的治疗方法,引起了人们的极大兴趣。传统的TPD降解剂依赖于小分子,这些小分子只能用已知的小分子结合剂或合适的结合袋靶向感兴趣蛋白(POI)。近年来,一些基于遗传信息的降解分子在细胞中表达的遗传编码TPD (GE-TPD)策略被开发出来。GE-TPD通过酵母和噬菌体展示等技术发现POI结合物,并通过遗传编码扩展E3连接酶工具箱。本文综述了近年来GE-TPD技术的进展,重点介绍了有潜力推动GE-TPD发展的创新技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Opinion in Biomedical Engineering
Current Opinion in Biomedical Engineering Medicine-Medicine (miscellaneous)
CiteScore
8.60
自引率
2.60%
发文量
59
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