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三聚体 G 蛋白 α-亚基 - 结构、肽衍生抑制剂和机制。

Heterotrimeric G Protein α-Subunits - Structures, Peptide-Derived Inhibitors, and Mechanisms.

机构信息

PharmaCenter Bonn, Pharmaceutical Institute, Pharmaceutical & Medicinal Chemistry, University of Bonn, An der Immenburg 4, D-53121 Bonn, Germany.

出版信息

Curr Med Chem. 2022;29(42):6359-6378. doi: 10.2174/0929867329666220308112424.

Abstract

G protein-coupled receptors are the largest protein family in the human body and represent the most important class of drug targets. They receive extracellular signals and transduce them into the cytosol. The guanine nucleotide-binding Gα proteins represent the main relays by which GPCRs induce intracellular effects. More than 800 different GPCRs interact with 16 Gα proteins belonging to 4 families, Gα, Gα, Gα, and Gα. The direct inhibition of Gα protein subunits rather than the modulation of GPCR subtypes has been proposed as a novel strategy for the treatment of complex diseases, including inflammation and cancer. This mini-review presents an introduction to G protein structure and function and describes achievements in the development of peptidic and peptide-derived Gα protein inhibitors. They have become indispensable pharmacological tools, and some of them exhibit significant potential as future drugs.

摘要

G 蛋白偶联受体是人体内最大的蛋白质家族,也是最重要的一类药物靶点。它们接收细胞外信号并将其转导至细胞质。鸟苷酸结合 Gα 蛋白是 GPCR 诱导细胞内效应的主要中继器。超过 800 种不同的 GPCR 与属于 4 个家族的 16 种 Gα 蛋白相互作用,Gα、Gα、Gα 和 Gα。直接抑制 Gα 蛋白亚基而不是调节 GPCR 亚型已被提议作为治疗包括炎症和癌症在内的复杂疾病的一种新策略。这篇小型综述介绍了 G 蛋白的结构和功能,并描述了肽和肽衍生的 Gα 蛋白抑制剂的开发成果。它们已成为不可或缺的药理学工具,其中一些作为未来药物具有显著的潜力。

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