Mutational analysis of G-protein coupled receptor--FFA2

Biochem Biophys Res Commun. 2011 Feb 4;405(1):122-7. doi: 10.1016/j.bbrc.2010.12.139. Epub 2011 Jan 7.

Abstract

FFA2 (GPR43) is a receptor for short-chain fatty acids (SCFAs), acetate, and propionate. FFA2 is predominantly expressed in islets, a subset of immune cells, adipocytes, and the gastrointestinal tract which suggest a possible role in inflammatory and metabolic conditions. We have previously described the identification and characterization of novel phenylacetamides as allosteric agonists of FFA2. In the current study, we have investigated the molecular determinants contributing to receptor activation with the endogenous and synthetic ligands as well as allosteric interactions between these two sites. The mutational analysis revealed previously unidentified sites that may allosterically regulate orthosteric ligand's function as well as residues potentially important for the interactions between orthosteric and allosteric binding sites.

MeSH terms

  • Allosteric Regulation
  • Animals
  • Binding Sites
  • DNA Mutational Analysis
  • HEK293 Cells
  • Humans
  • Ligands
  • Mutagenesis
  • Protein Conformation
  • Receptors, Cell Surface / agonists*
  • Receptors, Cell Surface / chemistry
  • Receptors, Cell Surface / genetics*

Substances

  • FFA2R protein, human
  • Ligands
  • Receptors, Cell Surface