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从沙利度胺到针对靶向蛋白降解的合理分子胶设计。

From Thalidomide to Rational Molecular Glue Design for Targeted Protein Degradation.

机构信息

Monte Rosa Therapeutics AG, Basel, Switzerland; email:

Ridgeline Therapeutics AG, Basel, Switzerland.

出版信息

Annu Rev Pharmacol Toxicol. 2024 Jan 23;64:291-312. doi: 10.1146/annurev-pharmtox-022123-104147. Epub 2023 Aug 16.

Abstract

Thalidomide and its derivatives are powerful cancer therapeutics that are among the best-understood molecular glue degraders (MGDs). These drugs selectively reprogram the E3 ubiquitin ligase cereblon (CRBN) to commit target proteins for degradation by the ubiquitin-proteasome system. MGDs create novel recognition interfaces on the surface of the E3 ligase that engage in induced protein-protein interactions with neosubstrates. Molecular insight into their mechanism of action opens exciting opportunities to engage a plethora of targets through a specific recognition motif, the G-loop. Our analysis shows that current CRBN-based MGDs can in principle recognize over 2,500 proteins in the human proteome that contain a G-loop. We review recent advances in tuning the specificity between CRBN and its MGD-induced neosubstrates and deduce a set of simple rules that govern these interactions. We conclude that rational MGD design efforts will enable selective degradation of many more proteins, expanding this therapeutic modality to more disease areas.

摘要

沙利度胺及其衍生物是强有力的癌症治疗药物,也是研究最为透彻的分子胶水降解剂(molecular glue degraders,MGD)之一。这些药物能选择性地重新编程 E3 泛素连接酶 cereblon(CRBN),使其将靶蛋白募集到泛素蛋白酶体系统进行降解。MGD 在 E3 连接酶的表面创建新的识别界面,与新的底物发生诱导的蛋白-蛋白相互作用。对其作用机制的分子理解为通过特定的识别基序(G 环)来靶向大量靶标提供了令人兴奋的机会。我们的分析表明,目前基于 CRBN 的 MGD 原则上可以识别人类蛋白质组中含有 G 环的超过 2500 种蛋白质。我们综述了在调节 CRBN 与其 MGD 诱导的新底物之间的特异性方面的最新进展,并推导出了一套控制这些相互作用的简单规则。我们的结论是,合理的 MGD 设计将能够选择性地降解更多的蛋白质,从而将这种治疗模式扩展到更多的疾病领域。

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