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Heterologous expression of G-protein-coupled receptors in yeast.
- Source :
-
Methods in enzymology [Methods Enzymol] 2015; Vol. 556, pp. 141-64. Date of Electronic Publication: 2015 Mar 20. - Publication Year :
- 2015
-
Abstract
- Heterologous yeast expression systems have been successfully used for the production of G-protein-coupled receptors (GPCRs) for both structural and functional studies. Yeast combine comparatively low cost and short culture times with straightforward generation of expression clones. They also perform some key posttranslational modifications not possible in bacterial systems. There are two major yeast expression systems, Pichia pastoris and Saccharomyces cerevisiae, both of which have been used for the production of GPCRs. P. pastoris has a proven track record for the production of large amounts of GPCR for structural studies. High-resolution crystal structures of both the adenosine A2A and the histamine H1 receptors have been obtained using protein expressed in this system. S. cerevisiae is relatively easy to engineer and this has resulted in the development of sophisticated tools for the functional characterization of GPCRs. In this chapter, we provide protocols for both large-scale receptor expression in P. pastoris for structural studies and small-scale receptor expression in S. cerevisiae for functional characterization. In both cases, the receptor used is the human adenosine A2A receptor. The results that both we and others have obtained using these protocols show the wide utility of the yeast expression systems for the production of GPCRs.<br /> (© 2015 Elsevier Inc. All rights reserved.)
- Subjects :
- Gene Expression
Humans
Microscopy, Confocal methods
Pichia growth & development
Plasmids genetics
Receptors, G-Protein-Coupled analysis
Recombinant Proteins analysis
Recombinant Proteins genetics
Saccharomyces cerevisiae growth & development
Cloning, Molecular methods
Pichia genetics
Receptors, G-Protein-Coupled genetics
Saccharomyces cerevisiae genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1557-7988
- Volume :
- 556
- Database :
- MEDLINE
- Journal :
- Methods in enzymology
- Publication Type :
- Academic Journal
- Accession number :
- 25857781
- Full Text :
- https://doi.org/10.1016/bs.mie.2014.11.046