Recombinant G Protein-Coupled Receptor Expression in Saccharomyces cerevisiae for Protein Characterization

被引:5
|
作者
Blocker, Kory M. [1 ]
Britton, Zachary T. [2 ]
Naranjo, Andrea N. [2 ]
McNeely, Patrick M. [2 ]
Young, Carissa L. [2 ]
Robinson, Anne S. [1 ,2 ]
机构
[1] Tulane Univ, Dept Chem & Biomol Engn, New Orleans, LA 70118 USA
[2] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE USA
关键词
EUKARYOTIC MEMBRANE-PROTEINS; ADENOSINE A2A RECEPTOR; HETEROLOGOUS EXPRESSION; PICHIA-PASTORIS; CELLULAR STRESS; YEAST; OVEREXPRESSION; OPTIMIZATION; PURIFICATION; SYSTEMS;
D O I
10.1016/bs.mie.2014.12.025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 A(2)a receptor and for reconstitution of the receptor in liposomes that have enabled its biophysical characterization.
引用
收藏
页码:165 / 183
页数:19
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