Bifunctional chemical probes inducing protein-protein interactions

被引:71
|
作者
Maniaci, Chiara [1 ,2 ]
Ciulli, Alessio [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Div Biol Chem & Drug Discovery, Dow St, Dundee DD1 5EH, Scotland
[2] Univ Oxford, Chem Res Lab, 12 Mansfield Rd, Oxford OX1 3TA, England
基金
欧洲研究理事会;
关键词
E3 UBIQUITIN LIGASE; PROTEOLYSIS-TARGETING CHIMERAS; STRUCTURE-GUIDED DESIGN; SMALL MOLECULES; SELECTIVE DEGRADATION; STRUCTURAL BASIS; INHIBITORS; BROMODOMAIN; DISCOVERY; OPTIMIZATION;
D O I
10.1016/j.cbpa.2019.07.003
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
Inducing biomolecular interactions with synthetic molecules to impact biological function is a concept of enormous appeal. Recent years have seen a resurgence of interest in designing bispecific molecules that serve as bridging agents to bring proteins together. Pioneering structural and biophysical investigation of ternary complexes formed by mono-functional and bifunctional ligands highlights that proximity-induced stabilization or de novo formation of protein-protein interactions is a common feature of their molecular recognition. In this review, we illustrate these concepts and advances with representative case studies, and highlight progress over the past three years, with particular focus on recruitment to E3 ubiquitin ligases by 'molecular glues' and chimeric dimerizers (PROTACs) for targeted protein degradation. This approach promises to significantly expand the range of tractable targets for chemical biology and therapeutic intervention.
引用
收藏
页码:145 / 156
页数:12
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