Structures of metabotropic GABABreceptor

Abstract

AbstractGABA (γ-aminobutyric acid) stimulation of the metabotropic GABABreceptor results in prolonged inhibition of neurotransmission that is central to brain physiology. GABABbelongs to the Family C of G protein-coupled receptors (GPCRs), which operate as dimers to relay synaptic neurotransmitter signals into a cellular response through the binding and activation of heterotrimeric G proteins. GABAB, however, is unique in its function as an obligate heterodimer in which agonist binding and G protein activation take place on distinct subunits. Here we show structures of heterodimeric and homodimeric full-length GABABreceptors. Complemented by cellular signaling assays and atomistic simulations, the structures reveal an essential role for the GABABextracellular loop 2 (ECL2) in relaying structural transitions by ordering the linker connecting the extracellular ligand-binding domain to the transmembrane region. Furthermore, the ECL2 of both GABABsubunits caps and interacts with the hydrophilic head of a phospholipid occupying the extracellular half of the transmembrane domain, thereby providing a potentially crucial link between ligand binding and the receptor core that engages G protein. These results provide a starting framework to decipher mechanistic modes of signal transduction mediated by GABABdimers and have important implications for rational drug design targeting these receptors.