Blocker Kory M, Britton Zachary T, Naranjo Andrea N, McNeely Patrick M, Young Carissa L, Robinson Anne S
Department of Chemical and Biomolecular Engineering, Tulane University, New Orleans, Louisiana, USA.
Department of Chemical and Biomolecular Engineering, University of Delaware, Newark, Delaware, USA.
Methods Enzymol. 2015;556:165-83. doi: 10.1016/bs.mie.2014.12.025. Epub 2015 Mar 20.
G protein-coupled receptors (GPCRs) are membrane proteins that mediate signaling across the cellular membrane and facilitate cellular responses to external stimuli. Due to the critical role that GPCRs play in signal transduction, therapeutics have been developed to influence GPCR function without an extensive understanding of the receptors themselves. Closing this knowledge gap is of paramount importance to improving therapeutic efficacy and specificity, where efforts to achieve this end have focused chiefly on improving our knowledge of the structure-function relationship. The purpose of this chapter is to review methods for the heterologous expression of GPCRs in Saccharomyces cerevisiae, including whole-cell assays that enable quantitation of expression, localization, and function in vivo. In addition, we describe methods for the micellular solubilization of the human adenosine A2a receptor and for reconstitution of the receptor in liposomes that have enabled its biophysical characterization.
G蛋白偶联受体(GPCRs)是跨细胞膜介导信号传导并促进细胞对外部刺激作出反应的膜蛋白。由于GPCRs在信号转导中发挥关键作用,因此在对这些受体本身没有深入了解的情况下就已开发出影响GPCR功能的疗法。弥合这一知识差距对于提高治疗效果和特异性至关重要,为此所做的努力主要集中在增进我们对结构-功能关系的认识上。本章的目的是综述在酿酒酵母中异源表达GPCRs的方法,包括能够在体内对表达、定位和功能进行定量的全细胞分析。此外,我们还描述了人腺苷A2a受体的微细胞增溶方法以及该受体在脂质体中的重构方法,这些方法使其能够进行生物物理特性表征。