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用荧光配体探究G蛋白偶联受体的药理学。

Probing the pharmacology of G protein-coupled receptors with fluorescent ligands.

作者信息

Stoddart Leigh A, Kilpatrick Laura E, Briddon Stephen J, Hill Stephen J

机构信息

Cell Signalling Research Group, School of Life Sciences, University of Nottingham, Nottingham, UK.

出版信息

Neuropharmacology. 2015 Nov;98:48-57. doi: 10.1016/j.neuropharm.2015.04.033. Epub 2015 May 13.

Abstract

G protein-coupled receptors control a wide range of physiological processes and are the target for many clinically used drugs. Understanding the way in which receptors bind agonists and antagonists, their organisation in the membrane and their regulation after agonist binding are important properties which are key to developing new drugs. One way to achieve this knowledge is through the use of fluorescent ligands, which have been used to study the expression and function of receptors in endogenously expressing systems. Fluorescent ligands with appropriate imaging properties can be used in conjunction with confocal microscopy to investigate the regulation of receptors after activation. Alternatively, through the use of single molecule microscopy, they can probe the spatial organisation of receptors within the membrane. This review focuses on the techniques in which fluorescent ligands have been used and the novel aspects of G protein-coupled receptor pharmacology which have been uncovered. This article is part of the Special Issue entitled 'Fluorescent Tools in Neuropharmacology'.

摘要

G蛋白偶联受体控制着广泛的生理过程,是许多临床用药的靶点。了解受体与激动剂和拮抗剂的结合方式、它们在膜中的组织形式以及激动剂结合后的调节机制,这些重要特性是开发新药的关键。获取这些知识的一种方法是使用荧光配体,荧光配体已被用于研究内源性表达系统中受体的表达和功能。具有适当成像特性的荧光配体可与共聚焦显微镜结合使用,以研究受体激活后的调节机制。或者,通过使用单分子显微镜,它们可以探测膜内受体的空间组织形式。本综述重点关注使用荧光配体的技术以及由此揭示的G蛋白偶联受体药理学的新方面。本文是名为“神经药理学中的荧光工具”的特刊的一部分。

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