Abstract

Heptahelical receptors activate intracellular signaling pathways by catalyzing GTP for GDP exchange on the heterotrimeric G protein α subunit (Gα). Despite the crucial role of this process in cell signaling, little is known about the mechanism of G protein activation. Here we explore the structural basis for receptor-mediated GDP release using electron paramagnetic resonance spectroscopy. Binding to the activated receptor (R|[ast]|) causes an apparent rigid-body movement of the α5 helix of Gα that would perturb GDP binding at the β6-α5 loop. This movement was not observed when a flexible loop was inserted between the α5 helix and the R|[ast]|-binding C terminus, which uncouples R|[ast]| binding from nucleotide exchange, suggesting that this movement is necessary for GDP release. These data provide the first direct observation of R|[ast]|-mediated conformational changes in G proteins and define the structural basis for GDP release from Gα.