Reconstitution of membrane proteins: a GPCR as an example

Goddard, Alan, Dijkman, Patricia, Adamson, Roslin , Dos Reis, Rosana and Watts, Anthony (2015) Reconstitution of membrane proteins: a GPCR as an example. Methods in Enzymology, 556 . pp. 405-424. ISSN 0076-6879

Full text not available from this repository.

Item Type:Article
Item Status:Live Archive


Membrane proteins are the gatekeepers to the cell and are essential to the function of all cells, controlling the flow of molecules and information across the cell membrane. Much effort has been put into the development of systems for studying membrane proteins in simplified environments that nevertheless mimic their native lipid environment. After isolation and production of purified membrane proteins in detergent, it is often necessary to reconstitute them into a lipid structure such as liposome, nanodisc, or lipodisq. Each of these has the advantage of returning the protein to a defined lipid environment, and the choice of system depends on the application. Regardless of the system to be used, the fundamental process involves the removal of detergent and incorporation of the protein into a stable lipid system. This chapter details methodologies we have developed, mainly focussed on the model G protein-coupled receptor (GPCR) neurotensin receptor 1, and the GPCR-homologue and model, bacteriorhopdopsin.

Additional Information:Elsevier Monograph series Membrane Proteins—Production and Functional Characterization
Keywords:Bacteriorhopdopsin; Cell membrane; G protein-coupled receptor; GPCR-homologue; Lipid structure; Membrane proteins; Neurotensin receptor 1, bmjgoldcheck, NotOAChecked
Subjects:C Biological Sciences > C770 Biophysical Science
C Biological Sciences > C790 Molecular Biology, Biophysics and Biochemistry not elsewhere classified
Divisions:College of Science > School of Life Sciences
Related URLs:
ID Code:17171
Deposited On:16 Apr 2015 15:19

Repository Staff Only: item control page