A Robust and Rapid Method of Producing Soluble, Stable, and Functional G-Protein Coupled Receptors

• Main Authors: Baaske, Philipp (Author), Geissler, Sandra (Author), Wienken, Christoph J. (Author), Jerabek-Willemsen, Moran (Author), Duhr, Stefan (Author), Braun, Dieter (Author), Corin, Karolina A. (Contributor), Ravel, Deepali B. (Contributor), Song, Junyao (Contributor), Brown, Emily E. (Contributor), Wang, Xiaoqiang (Contributor), Zhang, Shuguang (Contributor)
• Other Authors: Massachusetts Institute of Technology. Center for Biomedical Engineering (Contributor), Massachusetts Institute of Technology. Department of Biological Engineering (Contributor), Massachusetts Institute of Technology. Department of Biology (Contributor)
• Format: Article
• Language: English
• Published: Public Library of Science, 2012-02-10T17:28:07Z.
• Subjects: Article
• Online Access: Get fulltext

 Membrane proteins, particularly G-protein coupled receptors (GPCRs), are notoriously difficult to express. Using commercial E.coli cell-free systems with the detergent Brij-35, we could rapidly produce milligram quantities of 13 unique GPCRs. Immunoaffinity purification yielded receptors at >90% purity. Secondary structure analysis using circular dichroism indicated that the purified receptors were properly folded. Microscale thermophoresis, a novel label-free and surface-free detection technique that uses thermal gradients, showed that these receptors bound their ligands. The secondary structure and ligand-binding results from cell-free produced proteins were comparable to those expressed and purified from HEK293 cells. Our study demonstrates that cell-free protein production using commercially available kits and optimal detergents is a robust technology that can be used to produce sufficient GPCRs for biochemical, structural, and functional analyses. This robust and simple method may further stimulate others to study the structure and function of membrane proteins.