PT  - JOURNAL ARTICLE
AU  - Masataka Yanagawa
AU  - Takahiro Yamashita
AU  - Yoshinori Shichida
TI  - Activation Switch in the Transmembrane Domain of Metabotropic Glutamate Receptor
AID  - 10.1124/mol.109.056549
DP  - 2009 Jul 01
TA  - Molecular Pharmacology
PG  - 201--207
VI  - 76
IP  - 1
4099  - http://molpharm.aspetjournals.org/content/76/1/201.short
4100  - http://molpharm.aspetjournals.org/content/76/1/201.full
SO  - Mol Pharmacol2009 Jul 01; 76
AB  - Metabotropic glutamate receptors (mGluRs), members of family 3 G protein-coupled receptors, play pivotal roles in the modulation of synaptic transmission and are important drug targets for various neurological diseases. The structures of the extracellular ligand-binding domain (ECD) of mGluRs and its changes upon ligand binding have been well studied by various techniques, including X-ray crystallography. In contrast, little is known about the structure and structural changes of the seven-transmembrane domain (TMD). Here we searched for constitutively active mutation (CAM) sites in the TMD of mGluR8 to get insight into the epicenter of the structural changes in TMD, a potential target for allosteric ligands. Mutational analyses based on the knowledge of activating mutations of calcium-sensing receptor showed the presence of several CAM sites in the TMD of mGluR8. Among them, the site at position 764 in helix V, where threonine is present, is unique in that any substitution resulted in elevation of the basal activity, and some substitutions caused a loss of responsiveness to agonist. Further comprehensive mutational analyses indicated that the additional mutation of the CAM site at position 663 in helix III, where a tyrosine residue is present, generated a revertant phenotype. Mutations at these sites also increased the agonist binding affinity, although these sites are far from the ECD. These results indicated that the specific pair of amino acids at these CAM sites forms an activation switch that stabilizes the inactive state of mGluR8 and mediates the signal flow from the ECD to the cytoplasmic G protein-interacting site.