Molecular glues for protein-protein interactions Progressing toward a new dream

被引:13
|
作者
Konstantinidou, Markella [1 ,2 ]
Arkin, Michelle R. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Small Mol Discovery Ctr SMDC, San Francisco, CA 94143 USA
关键词
ELEMENT-BINDING PROTEIN; E3 UBIQUITIN LIGASE; STRUCTURAL BASIS; SELECTIVE DEGRADATION; RBM39; RECRUITMENT; DRUG DISCOVERY; TARGET; INHIBITORS; COMPLEX; LENALIDOMIDE;
D O I
10.1016/j.chembiol.2024.04.002
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
The modulation of protein-protein interactions with small molecules is one of the most rapidly developing areas in drug discovery. In this review, we discuss advances over the past decade (2014-2023) focusing on molecular glues (MGs)-monovalent small molecules that induce proximity, either by stabilizing native interactions or by inducing neomorphic interactions. We include both serendipitous and rational discoveries and describe the different approaches that were used to identify them. We classify the compounds in three main categories: degradative MGs, non-degradative MGs or PPI stabilizers, and MGs that induce self-association. Diverse, illustrative examples with structural data are described in detail, emphasizing the elements of molecular recognition and cooperative binding at the interface that are fundamental for a MG mechanism of action.
引用
收藏
页码:1064 / 1088
页数:25
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