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运用全局磷酸化蛋白质组学揭示 G 蛋白偶联受体信号转导网络。

Unravelling G protein-coupled receptor signalling networks using global phosphoproteomics.

机构信息

Department of Biochemistry & Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.

QIMR Berghofer Medical Research Institute, Herston, QLD, Australia.

出版信息

Br J Pharmacol. 2024 Jul;181(14):2359-2370. doi: 10.1111/bph.16052. Epub 2023 Feb 24.

Abstract

G protein-coupled receptor (GPCR) activation initiates signalling via a complex network of intracellular effectors that combine to produce diverse cellular and tissue responses. Although we have an advanced understanding of the proximal events following receptor stimulation, the molecular detail of GPCR signalling further downstream often remains obscure. Unravelling these GPCR-mediated signalling networks has important implications for receptor biology and drug discovery. In this context, phosphoproteomics has emerged as a powerful approach for investigating global GPCR signal transduction. Here, we provide a brief overview of the phosphoproteomic workflow and discuss current limitations and future directions for this technology. By highlighting some of the novel insights into GPCR signalling networks gained using phosphoproteomics, we demonstrate the utility of global phosphoproteomics to dissect GPCR signalling networks and to accelerate discovery of new targets for therapeutic development. LINKED ARTICLES: This article is part of a themed issue Therapeutic Targeting of G Protein-Coupled Receptors: hot topics from the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists 2021 Virtual Annual Scientific Meeting. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.

摘要

G 蛋白偶联受体 (GPCR) 的激活通过细胞内效应器的复杂网络引发信号转导,这些效应器组合在一起产生不同的细胞和组织反应。尽管我们对受体刺激后的近端事件有了深入的了解,但 GPCR 信号转导的下游分子细节往往仍然不清楚。揭示这些 GPCR 介导的信号网络对受体生物学和药物发现具有重要意义。在这种情况下,磷酸蛋白质组学已成为研究全局 GPCR 信号转导的一种强大方法。在这里,我们简要概述了磷酸蛋白质组学的工作流程,并讨论了该技术的当前限制和未来方向。通过强调使用磷酸蛋白质组学获得的一些关于 GPCR 信号网络的新见解,我们证明了全局磷酸蛋白质组学在剖析 GPCR 信号网络以及加速发现新的治疗靶点方面的实用性。相关文章:本文是 2021 年澳大利亚临床和实验药理学和毒理学学会虚拟年会主题特刊中“G 蛋白偶联受体治疗靶向:热点话题”的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.

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