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G 蛋白偶联受体的疗效本质。

The nature of efficacy at G protein-coupled receptors.

机构信息

Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences and Department of Pharmacology, Monash University, Parkville, Victoria 3052, Australia.

出版信息

Biochem Pharmacol. 2019 Dec;170:113647. doi: 10.1016/j.bcp.2019.113647. Epub 2019 Oct 1.

Abstract

G protein-coupled receptors (GPCRs) participate in many pathophysiological processes as well as almost all aspects of normal physiology. They are present at the surface of all cell types making them amenable and attractive targets for pharmaceutical therapeutics. GPCRs possess complex pharmacology with the ability to be turned on to various extents, have their constitutive activity suppressed and even switch between signaling pathways to which they couple. Underlying this complex pharmacology is GPCR signaling efficacy, and differences in efficacy promoted by alternative ligands and in different tissues is of great interest to biology in general and also the pharmaceutical industry. In this review we hope to discuss what the molecular foundations of efficacy are and whether a new approach utilizing a rate-dependent model may provide new insights into this phenomenon.

摘要

G 蛋白偶联受体(GPCRs)参与许多病理生理过程以及正常生理的几乎所有方面。它们存在于所有细胞类型的表面,使它们成为药物治疗的合适且有吸引力的靶点。GPCR 具有复杂的药理学特性,能够在不同程度上被激活,其组成性活性受到抑制,甚至在它们耦联的信号通路之间切换。这种复杂的药理学特性的基础是 GPCR 信号转导效率,不同配体和不同组织中效率的差异引起了生物学界和制药工业的极大兴趣。在这篇综述中,我们希望讨论效率的分子基础是什么,以及利用速率依赖性模型的新方法是否可以为这一现象提供新的见解。

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