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蛋白-蛋白相互作用及其相关抑制剂与 NLRP3 炎症小体途径有关。

Protein-protein interactions and related inhibitors involved in the NLRP3 inflammasome pathway.

机构信息

Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China; Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing 210009, China.

Jiangsu Key Laboratory of Drug Design and Optimization, China Pharmaceutical University, Nanjing 210009, China; Key Laboratory of Drug Quality Control and Pharmacovigilance, Ministry of Education, China Pharmaceutical University, Nanjing 210009, China.

出版信息

Cytokine Growth Factor Rev. 2023 Dec;74:14-28. doi: 10.1016/j.cytogfr.2023.09.003. Epub 2023 Sep 16.

Abstract

NOD-like receptor thermal protein domain-associated protein 3 (NLRP3) receptor serves as the central node of immune sensing in the innate immune system, and plays an important role in the initiation and progression of chronic diseases. Cryo-electron microscopy (cryo-EM) has provided insights into the conformation of various oligomers within the NLRP3 activation pathway, significantly advancing our understanding of the mechanisms underlying NLRP3 inflammasome activation. Despite the extensive network of protein-protein interactions (PPIs) involved in the assembly and activation of NLRP3 inflammasome, the utilization of protein-protein interactions has been relatively overlooked in the development of NLRP3 inhibitors. This review focuses on summarizing PPIs within the NLRP3 inflammasome activation pathway and small molecule inhibitors capable of interfering with PPIs to counteract the NLRP3 overactivation. Small molecule NLRP3 inhibitors have been gained significant attention owing to their remarkable efficacy, excellent safety profiles, and unique mechanisms of action.

摘要

核苷酸结合寡聚结构域样受体热蛋白结构域相关蛋白 3(NLRP3)受体作为先天免疫系统中免疫感应的核心节点,在慢性疾病的发生和发展中发挥着重要作用。低温电子显微镜(cryo-EM)技术为 NLRP3 激活途径中各种寡聚体的构象提供了深入了解,极大地促进了我们对 NLRP3 炎性小体激活机制的认识。尽管在 NLRP3 炎性小体的组装和激活过程中涉及广泛的蛋白质-蛋白质相互作用(PPIs)网络,但在 NLRP3 抑制剂的开发中,对蛋白质-蛋白质相互作用的利用相对被忽视。本综述重点总结了 NLRP3 炎性小体激活途径中的 PPIs 以及能够干扰 PPIs 以拮抗 NLRP3 过度激活的小分子抑制剂。小分子 NLRP3 抑制剂由于其显著的疗效、良好的安全性和独特的作用机制而备受关注。

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