RT Journal Article
SR Electronic
T1 Identification and Pharmacological Characterization of Multiple Allosteric Binding Sites on the FFA1 Receptor
JF Molecular Pharmacology
JO Mol Pharmacol
FD American Society for Pharmacology and Experimental Therapeutics
SP mol.112.079640
DO 10.1124/mol.112.079640
A1 Daniel Lin
A1 Qi Guo
A1 Jian Luo
A1 Jane Zhang
A1 Kathy Nguyen
A1 Michael Chen
A1 Thanh Tran
A1 Paul J Dransfield
A1 Sean P Brown
A1 Jonathan Houze
A1 Marc Vimolratana
A1 Xian Yun Jiao
A1 Yingcai Wang
A1 Nigel J.M. Birdsall
A1 Gayathri Swaminath
YR 2012
UL http://molpharm.aspetjournals.org/content/early/2012/08/02/mol.112.079640.abstract
AB Abstract Activation of FFA1 (GPR40), a member of GPCR family A, is mediated by medium and long chain fatty acids and leads to amplification of glucose stimulated insulin secretion, suggesting a potential role for FFA1 as a target for type 2 diabetes. It has been previously assumed that there is a single binding site for fatty acids and synthetic FFA1 agonists. However, using members of two chemical series of partial and full agonists that have been identified, radioligand binding interaction studies revealed that the full agonists do not bind to the same site as the partial agonists but exhibit positive heterotropic cooperativity. Analysis of functional data reveals positive functional cooperativity between the full agonists and partial agonists in various functional assays (in vitro and ex vivo) and also in vivo. Furthermore, the endogenous fatty acid, docosahexaenoic acid (DHA) shows negative or neutral cooperativity with members of both series of agonists in binding assays but displays positive cooperativity in functional assays. Another synthetic agonist is allosteric with members of both agonist series, but apparently competitive with DHA. Therefore there appear to be three allosterically-linked binding sites on FFA1 with agonists specific for each of these sites. Activation of FFAR1 by each of these agonists is differentially affected by mutations of two arginine residues, previously found to be important of FFAR1 binding and activation. The high potencies of these ligands and their strong positive functional cooperativity with endogenous fatty acids, demonstrated in vitro and in vivo, has the potential to deliver therapeutic benefits.