Detection of G Protein-selective G Protein-coupled Receptor (GPCR) Conformations in Live Cells

Although several recent studies have reported that GPCRs adopt multiple conformations, it remains unclear how subtle conformational changes are translated into divergent downstream responses. In this study, we report on a novel class of FRET-based sensors that can detect the ligand/mutagenic stabilization of GPCR conformations that promote interactions with G proteins in live cells. These sensors rely on the well characterized interaction between a GPCR and the C terminus of a G alpha subunit. We use these sensors to elucidate the influence of the highly conserved (E/D) RY motif on GPCR conformation. Specifically, Glu/Asp but not Arg mutants of the (E/D) RY motif are known to enhance basal GPCR signaling. Hence, it is unclear whether ionic interactions formed by the (E/D) RY motif ( ionic lock) are necessary to stabilize basal GPCR states. We find that mutagenesis of the beta 2-AR (E/D) RY ionic lock enhances interaction with G(s). However, only Glu/Asp but not Arg mutants increase G protein activation. In contrast, mutagenesis of the opsin (E/D) RY ionic lock does not alter its interaction with transducin. Instead, opsin-specific ionic interactions centered on residue Lys-296 are both necessary and sufficient to promote interactions with transducin. Effective suppression of beta 2-AR basal activity by inverse agonist ICI 118,551 requires ionic interactions formed by the (E/D) RY motif. In contrast, the inverse agonist metoprolol suppresses interactions with G(s) and promotes G(i) binding, with concomitant pertussis toxin-sensitive inhibition of adenylyl cyclase activity. Taken together, these studies validate the use of the new FRET sensors while revealing distinct structural mechanisms for ligand-dependent GPCR function.