Suppr超能文献

G蛋白偶联受体在脂筏中的定位与信号传导

Localization and signaling of GPCRs in lipid rafts.

作者信息

Villar Van Anthony M, Cuevas Santiago, Zheng Xiaoxu, Jose Pedro A

机构信息

Division of Renal Diseases & Hypertension, Department of Medicine, The George Washington University School of Medicine and Health Sciences, WA, USA.

出版信息

Methods Cell Biol. 2016;132:3-23. doi: 10.1016/bs.mcb.2015.11.008. Epub 2016 Feb 10.

Abstract

The understanding of how biological membranes are organized and how they function has evolved. Instead of just serving as a medium in which certain proteins are found, portions of the lipid bilayer have been demonstrated to form specialized platforms that foster the assembly of signaling complexes by providing a microenvironment that is conducive for effective protein-protein interactions. G protein-coupled receptors (GPCRs) and relevant signaling molecules, including the heterotrimeric G proteins, key enzymes such as kinases and phosphatases, trafficking proteins, and secondary messengers, preferentially partition to these highly organized cell membrane microdomains, called lipid rafts. As such, lipid rafts are crucial for the trafficking and signaling of GPCRs. The study of GPCR biology in the context of lipid rafts involves the localization of the GPCR of interest in lipid rafts, at the basal state and upon receptor agonism, and the evaluation of the biological functions of the GPCR in appropriate cell lines. The lack of standardized methodology to study lipid rafts, in general, and of the workings of GPCRs in lipid rafts, in particular, and the inherent drawbacks of current methods have hampered the complete understanding of the underlying molecular mechanisms. Newer methodologies that allow the study of GPCRs in their native form are needed. The use of complementary approaches that produce mutually supportive results appear to be the best way for drawing conclusions with regards to the distribution and activity of GPCRs in lipid rafts.

摘要

对生物膜如何组织及其功能的理解已经有所发展。脂质双层的某些部分不再仅仅作为某些蛋白质存在的介质,而是已被证明能形成特殊的平台,通过提供有利于有效蛋白质 - 蛋白质相互作用的微环境来促进信号复合物的组装。G蛋白偶联受体(GPCRs)和相关信号分子,包括异源三聚体G蛋白、关键酶如激酶和磷酸酶、转运蛋白以及第二信使,优先分配到这些高度组织化的细胞膜微结构域,即脂筏。因此,脂筏对于GPCRs的转运和信号传导至关重要。在脂筏背景下研究GPCR生物学涉及在基础状态和受体激动时,将感兴趣的GPCR定位在脂筏中,并在合适的细胞系中评估GPCR的生物学功能。总体而言,缺乏研究脂筏的标准化方法,尤其是缺乏研究脂筏中GPCRs作用机制的方法,以及现有方法的固有缺陷,阻碍了对潜在分子机制的全面理解。需要更新的方法来研究天然形式的GPCRs。使用能产生相互支持结果的互补方法似乎是得出关于GPCRs在脂筏中的分布和活性结论的最佳方式。

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