Suppr超能文献

毒蕈碱型乙酰胆碱受体寡聚化。

Muscarinic receptor oligomerization.

机构信息

Centre for Translational Pharmacology, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, Scotland, UK.

Centre for Translational Pharmacology, Institute of Molecular, Cell and Systems Biology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow G12 8QQ, Scotland, UK.

出版信息

Neuropharmacology. 2018 Jul 1;136(Pt C):401-410. doi: 10.1016/j.neuropharm.2017.11.023. Epub 2017 Nov 14.

Abstract

G protein-coupled receptors (GPCRs) have been classically described as monomeric entities that function by binding in a 1:1 stoichiometric ratio to both ligand and downstream signalling proteins. However, in recent years, a growing number of studies has supported the hypothesis that these receptors can interact to form dimers and higher order oligomers although the molecular basis for these interactions, the overall quaternary arrangements and the functional importance of GPCR oligomerization remain topics of intense speculation. Muscarinic acetylcholine receptors belong to class A of the GPCR family. Each muscarinic receptor subtype has its own particular distribution throughout the central and peripheral nervous systems. In the central nervous system, muscarinic receptors regulate several sensory, cognitive, and motor functions while, in the peripheral nervous system, they are involved in the regulation of heart rate, stimulation of glandular secretion and smooth muscle contraction. Muscarinic acetylcholine receptors have long been used as a model for the study of GPCR structure and function and to address aspects of GPCR dimerization using a broad range of approaches. In this review, the prevailing knowledge regarding the quaternary arrangement for the various muscarinic acetylcholine receptors has been summarized by discussing work ranging from initial results obtained using more traditional biochemical approaches to those generated with more modern biophysical techniques. This article is part of the Special Issue entitled 'Neuropharmacology on Muscarinic Receptors'.

摘要

G 蛋白偶联受体 (GPCRs) 传统上被描述为单体实体,通过以 1:1 的化学计量比与配体和下游信号蛋白结合来发挥作用。然而,近年来,越来越多的研究支持了这样一种假设,即这些受体可以相互作用形成二聚体和更高阶的寡聚体,尽管这些相互作用的分子基础、整体四级结构以及 GPCR 寡聚化的功能重要性仍然是激烈推测的主题。毒蕈碱型乙酰胆碱受体属于 GPCR 家族的 A 类。每种毒蕈碱型受体亚型在中枢和外周神经系统中都有其特定的分布。在中枢神经系统中,毒蕈碱受体调节多种感觉、认知和运动功能,而在外周神经系统中,它们参与心率调节、腺体分泌刺激和平滑肌收缩。毒蕈碱型乙酰胆碱受体长期以来一直被用作 GPCR 结构和功能研究的模型,并使用广泛的方法研究 GPCR 二聚化的各个方面。在这篇综述中,通过讨论从最初使用更传统的生化方法获得的结果到使用更现代的生物物理技术获得的结果,总结了各种毒蕈碱型乙酰胆碱受体的四级排列的现有知识。本文是题为“毒蕈碱受体的神经药理学”的特刊的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c323/6078712/4c2bbc9936df/gr1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验