Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10843735 | Protein Expression and Purification | 2005 | 10 Pages |
Abstract
Understanding the three-dimensional structure of G protein-coupled receptors (GPCRs) has been limited by the technical challenges associated with expression, purification, and crystallization of membrane proteins, and their low abundance in native tissue. In the first large-scale comparative study of GPCR protein production using recombinant baculovirus, we report the characterization of 16 human receptors. The GPCRs were produced in three insect cell lines and functional protein levels monitored over 72Â h using radioligand binding assays. Different GPCRs exhibited widely different expression levels, ranging from less than 1Â pmol receptor/mg protein to more than 250Â pmol/mg. No single set of conditions was suitable for all GPCRs, and large differences were seen for the expression of individual GPCRs in different cell lines. Closely related GPCRs did not share similar expression profiles; however, high expression (greater than 20Â pmol/mg) was achieved for over half the GPCRs in our study. Overall, the levels of protein production compared favourably to other published systems.
Related Topics
Life Sciences
Biochemistry, Genetics and Molecular Biology
Biochemistry
Authors
Malika Akermoun, Markus Koglin, Darina Zvalova-Iooss, Nicolas Folschweiller, Simon J. Dowell, Katy L. Gearing,