Milligan, G., Feng, G.J., Ward, R.J., Sartania, N. , Ramsay, D., McLean, A.J. and Carrillo, J.J. (2004) G protein-coupled receptor fusion proteins in drug discovery. Current Pharmaceutical Design, 10(17), pp. 1989-2001. (doi: 10.2174/1381612043384295) (PMID:15279540)
Full text not currently available from Enlighten.
Publisher's URL: http://dx.doi.org/10.2174/1381612043384295
Abstract
A wide range of peptides and polypeptides can be appended to either the N- or C-terminus of G proteincoupled receptors without disrupting substantially ligand binding and signal transduction. Following fusion of fluorescent proteins, reporter gene constructs or G protein α subunits to the C-terminal tail of a receptor high content and G protein activation assays can be employed to identify agonist ligands. Further modification of the receptor fusions to introduce enhanced levels of constitutive activity and to physically destabilise the protein allows antagonist / inverse agonists screens to be developed in parallel. Equivalent C-terminal addition of pairs of complementary, non-functional, polypeptide fragments allows the application of enzyme complementation techniques. Introduction of N-terminal tags to receptors has also allowed the introduction of novel assay techniques based on a pH-sensitive cyanine dye. These have the capacity to overcome certain limitations of GPCR-fluorescent protein fusions.
Item Type: | Articles |
---|---|
Status: | Published |
Refereed: | Yes |
Glasgow Author(s) Enlighten ID: | Milligan, Professor Graeme and Sartania, Dr Nana |
Authors: | Milligan, G., Feng, G.J., Ward, R.J., Sartania, N., Ramsay, D., McLean, A.J., and Carrillo, J.J. |
College/School: | College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing |
Journal Name: | Current Pharmaceutical Design |
Publisher: | Bentham Science Publishers |
ISSN: | 1381-6128 |
ISSN (Online): | 1873-4286 |
Related URLs: |
University Staff: Request a correction | Enlighten Editors: Update this record