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“三体解决方案”:分子胶的结构见解

The "three body solution": Structural insights into molecular glues.

作者信息

Tomlinson Aidan C A, Knox John E, Brunsveld Luc, Ottmann Christian, Yano Jason K

机构信息

Revolution Medicines, Redwood City, CA, USA.

Eindhoven University of Technology, Eindhoven, Netherlands.

出版信息

Curr Opin Struct Biol. 2025 Apr;91:103007. doi: 10.1016/j.sbi.2025.103007. Epub 2025 Feb 26.

Abstract

Molecular glues are small molecules that nucleate novel or stabilize natural, protein-protein interactions resulting in a ternary complex. Their success in targeting difficult to drug proteins of interest has led to ever-increasing interest in their use as therapeutics and research tools. While molecular glues and their targets vary in structure, inspection of diverse ternary complexes reveals commonalities. Whether of high or low molecular weight, molecular glues are often rigid and form direct hydrophobic interactions with their target protein. There is growing evidence that these hotspots can accommodate multiple ternary complex binding modes and enable targeting of traditionally undruggable targets. Advances in screening from the molecular glue degrader literature and insights in structure-based drug design, especially from the non-degrading tri-complex work, are likely intersectional.

摘要

分子胶是一类小分子,它们能够促成新的蛋白质 - 蛋白质相互作用或稳定天然的蛋白质 - 蛋白质相互作用,从而形成三元复合物。它们在靶向难以成药的目标蛋白方面取得的成功,引发了人们对其作为治疗药物和研究工具的兴趣日益浓厚。虽然分子胶及其靶点在结构上各不相同,但对各种三元复合物的研究揭示了它们的共性。无论分子量大小,分子胶通常都具有刚性,并与其靶蛋白形成直接的疏水相互作用。越来越多的证据表明,这些热点可以容纳多种三元复合物结合模式,并能够靶向传统上难以成药的靶点。分子胶降解剂文献中的筛选进展以及基于结构的药物设计方面的见解,尤其是来自非降解三元复合物研究的见解,很可能相互交叉。

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