| Literature DB >> 24900622 |
Antonio Macchiarulo1, Antimo Gioiello1, Charles Thomas2, Thijs W H Pols2, Roberto Nuti3, Cristina Ferrari1, Nicola Giacchè3, Francesca De Franco3, Mark Pruzanski4, Johan Auwerx2, Kristina Schoonjans2, Roberto Pellicciari5.
Abstract
TGR5 is a G-protein-coupled receptor (GPCR) mediating cellular responses to bile acids (BAs). Although some efforts have been devoted to generate homology models of TGR5 and draw structure-activity relationships of BAs, none of these studies has hitherto described how BAs bind to TGR5. Here, we present an integrated computational, chemical, and biological approach that has been instrumental to determine the binding mode of BAs to TGR5. As a result, key residues have been identified that are involved in mediating the binding of BAs to the receptor. Collectively, these results provide new hints to design potent and selective TGR5 agonists.Entities:
Keywords: Bile acids; GPCR; TGR5; diabetes; homology modeling; molecular docking; site-directed mutagenesis
Year: 2013 PMID: 24900622 PMCID: PMC4027510 DOI: 10.1021/ml400247k
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345