Delineating a Ca2+ Binding Pocket within the Venus Flytrap Module of the Human Calcium-sensing Receptor

• Published in: The Journal of biological chemistry 2005-11, Vol.280 (45), p.37917-37923
• Main Authors: Silve, Caroline, Petrel, Christophe, Leroy, Christine, Bruel, Henri, Mallet, Eric, Rognan, Didier, Ruat, Martial
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Animals; Base Sequence; Binding Sites; Biochemistry, Molecular Biology; Calcium; Calcium - metabolism; Female; Humans; Life Sciences; Male; Mutation; Neurons and Cognition; Pedigree; Phylogeny; Rats; Receptors, AMPA; Receptors, AMPA - metabolism; Receptors, Calcium-Sensing; Receptors, Calcium-Sensing - chemistry; Receptors, Calcium-Sensing - genetics; Receptors, Calcium-Sensing - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M506263200

The Ca2+-sensing receptor (CaSR) belongs to the class III G-protein-coupled receptors (GPCRs), which include receptors for pheromones, amino acids, sweeteners, and the neurotransmitters glutamate and γ-aminobutyric acid (GABA). These receptors are characterized by a long extracellular amino-terminal domain called a Venus flytrap module (VFTM) containing the ligand binding pocket. To elucidate the molecular determinants implicated in Ca2+ recognition by the CaSR VFTM, we developed a homology model of the human CaSR VFTM from the x-ray structure of the metabotropic glutamate receptor type 1 (mGluR1), and a phylogenetic analysis of 14 class III GPCR VFTMs. We identified critical amino acids delineating a Ca2+ binding pocket predicted to be adjacent to, but distinct from, a cavity reminiscent of the binding site described for amino acids in mGluRs, GABA-B receptor, and GPRC6a. Most interestingly, these Ca2+-contacting residues are well conserved within class III GPCR VFTMs. Our model was validated by mutational and functional analysis, including the characterization of activating and inactivating mutations affecting a single amino acid, Glu-297, located within the proposed Ca2+ binding pocket of the CaSR and associated with autosomal dominant hypocalcemia and familial hypocalciuric hypercalcemia, respectively, genetic diseases characterized by perturbations in Ca2+ homeostasis. Altogether, these data define a Ca2+ binding pocket within the CaSR VFTM that may be conserved in several other class III GPCRs, thereby providing a molecular basis for extracellular Ca2+ sensing by these receptors.