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分子胶:能够结合蛋白质的小分子,可改变蛋白质-蛋白质相互作用和蛋白质组,从而有潜力治疗人类癌症和神经退行性疾病。

Molecular Glues: Capable Protein-Binding Small Molecules That Can Change Protein-Protein Interactions and Interactomes for the Potential Treatment of Human Cancer and Neurodegenerative Diseases.

机构信息

Department of Pharmacology & Therapeutics, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263, USA.

Developmental Therapeutics (DT) Program, Roswell Park Comprehensive Cancer Center, Buffalo, NY 14263, USA.

出版信息

Int J Mol Sci. 2022 Jun 1;23(11):6206. doi: 10.3390/ijms23116206.

Abstract

Molecular glue (MG) compounds are a type of unique small molecule that can change the protein-protein interactions (PPIs) and interactomes by degrading, stabilizing, or activating the target protein after their binging. These small-molecule MGs are gradually being recognized for their potential application in treating human diseases, including cancer. Evidence suggests that small-molecule MG compounds could essentially target any proteins, which play critical roles in human disease etiology, where many of these protein targets were previously considered undruggable. Intriguingly, most MG compounds with high efficacy for cancer treatment can glue on and control multiple key protein targets. On the other hand, a single key protein target can also be glued by multiple MG compounds with distinct chemical structures. The high flexibility of MG-protein interaction profiles provides rich soil for the growth and development of small-molecule MG compounds that can be used as molecular tools to assist in unraveling disease mechanisms, and they can also facilitate drug development for the treatment of human disease, especially human cancer. In this review, we elucidate this concept by using various types of small-molecule MG compounds and their corresponding protein targets that have been documented in the literature.

摘要

分子胶(MG)化合物是一种独特的小分子,它们可以在结合后通过降解、稳定或激活靶蛋白来改变蛋白质-蛋白质相互作用(PPIs)和互作组。这些小分子 MG 化合物因其在治疗人类疾病(包括癌症)方面的潜在应用而逐渐得到认可。有证据表明,小分子 MG 化合物可以从根本上靶向任何在人类疾病发病机制中起关键作用的蛋白质,而这些蛋白质靶标中有许多以前被认为是不可成药的。有趣的是,大多数具有高效抗癌作用的 MG 化合物可以黏附并控制多个关键蛋白靶标。另一方面,多个具有不同化学结构的 MG 化合物也可以黏附在单个关键蛋白靶标上。MG-蛋白相互作用谱的高灵活性为小分子 MG 化合物的生长和发展提供了丰富的土壤,这些化合物可以用作分子工具来帮助揭示疾病机制,也可以促进人类疾病(尤其是人类癌症)治疗药物的开发。在这篇综述中,我们使用文献中记录的各种类型的小分子 MG 化合物及其相应的蛋白靶标来说明这一概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96e9/9181451/668f036454a3/ijms-23-06206-g007.jpg

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