Present address: Anna-Karin Tunemalm, FOI CBRN Defence and Security, S-901 82 Umeå, Sweden.
Using Ligand-Based Virtual Screening to Allosterically Stabilize the Activated State of a GPCR
Article first published online: 19 JAN 2010
© 2010 John Wiley & Sons A/S
Chemical Biology & Drug Design
Volume 75, Issue 3, pages 325–332, March 2010
How to Cite
Taylor, C. M., Rockweiler, N. B., Liu, C., Rikimaru, L., Tunemalm, A.-K., Kisselev, O. G. and Marshall, G. R. (2010), Using Ligand-Based Virtual Screening to Allosterically Stabilize the Activated State of a GPCR. Chemical Biology & Drug Design, 75: 325–332. doi: 10.1111/j.1747-0285.2009.00944.x
- Issue published online: 25 JAN 2010
- Article first published online: 19 JAN 2010
- Received 7 November 2009, revised 8 December 2009 and accepted for publication 8 December 2009
- ligand-based virtual screening;
- MII stabilization;
G-protein coupled receptors play an essential role in many biological processes. Despite an increase in the number of solved X-ray crystal structures of G-protein coupled receptors, capturing a G-protein coupled receptor in its activated state for structural analysis has proven to be difficult. An unexplored paradigm is stabilization of one or more conformational states of a G-protein coupled receptor via binding a small molecule to the intracellular loops. A short tetrazole peptidomimetic based on the photoactivated state of rhodopsin-bound structure of Gtα(340–350) was previously designed and shown to stabilize the photoactivated state of rhodopsin, the G-protein coupled receptor involved in vision. A pharmacophore model derived from the designed tetrazole tetrapeptide was used for ligand-based virtual screening to enhance the possible discovery of novel scaffolds. Maybridge Hitfinder and National Cancer Institute diversity libraries were screened for compounds containing the pharmacophore. Forty-seven compounds resulted from virtually screening the Maybridge library, whereas no hits resulted with the National Cancer Institute library. Three of the 47 Maybridge compounds were found to stabilize the MII state. As these compounds did not inhibit binding of transducin to photoactivated state of rhodopsin, they were assumed to be allosteric ligands. These compounds are potentially useful for crystallographic studies where complexes with these compounds might capture rhodopsin in its activated conformational state.