Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2015 Aug 3:81:29.14.1-29.14.29.
doi: 10.1002/0471140864.ps2914s81.

Cell-Free Expression of G Protein-Coupled Receptors

Affiliations

Cell-Free Expression of G Protein-Coupled Receptors

Kenneth Segers et al. Curr Protoc Protein Sci. .

Abstract

The large-scale production of recombinant G protein-coupled receptors (GPCRs) is one of the major bottlenecks that hamper functional and structural studies of this important class of integral membrane proteins. Heterologous overexpression of GPCRs often results in low yields of active protein, usually due to a combination of several factors, such as low expression levels, protein insolubility, host cell toxicity, and the need to use harsh and often denaturing detergents (e.g., SDS, LDAO, OG, and DDM, among others) to extract the recombinant receptor from the host cell membrane. Many of these problematic issues are inherently linked to cell-based expression systems and can therefore be circumvented by the use of cell-free systems. In this unit, we provide a range of protocols for the production of GPCRs in a cell-free expression system. Using this system, we typically obtain GPCR expression levels of ∼1 mg per ml of reaction mixture in the continuous-exchange configuration. Although the protocols in this unit have been optimized for the cell-free expression of GPCRs, they should provide a good starting point for the production of other classes of membrane proteins, such as ion channels, aquaporins, carrier proteins, membrane-bound enzymes, and even large molecular complexes.

Keywords: E. coli extract; GPCR; cell-free expression; detergent; lipid; membrane protein.

PubMed Disclaimer

References

Literature Cited

    1. Ahn, J.H. , Hwang, M.Y. , Lee, K.H. , Choi, C.Y. , and Kim, D.M. 2007. Use of signal sequences as an in situ removable sequence element to stimulate protein synthesis in cell-free extracts. Nucleic Acids Res. 35:e21.
    1. Anastasina, M. , Terenin, I. , Butcher, S.J. , and Kainov, D.E. 2014. A technique to increase protein yield in a rabbit reticulocyte lysate translation system. Biotechniques 56:36-39.
    1. Andrell, J. and Tate, C.G. 2013. Overexpression of membrane proteins in mammalian cells for structural studies. Mol. Membrane Biol. 30:52-63.
    1. Ausubel, F.M. , Brent, R. , Kingston, R.E. , Moore, D.D. , Seidman, J.G. , Smith, J.A. , and Struhl, K. , (eds). 2015. Current Protocols in Molecular Biology. John Wiley & Sons, Hoboken, N.J.
    1. Bernhard, F. and Tozawa, Y. 2013. Cell-free expression-making a mark. Curr. Opin. Struct. Biol. 23:374-380.

MeSH terms

LinkOut - more resources