RT Journal Article SR Electronic T1 Structural basis for regulation of human calcium-sensing receptor by magnesium ions and an unexpected tryptophan derivative co-agonist JF Science Advances JO Sci Adv FD American Association for the Advancement of Science SP e1600241 DO 10.1126/sciadv.1600241 VO 2 IS 5 A1 Zhang, Chen A1 Zhang, Tuo A1 Zou, Juan A1 Miller, Cassandra Lynn A1 Gorkhali, Rakshya A1 Yang, Jeong-Yeh A1 Schilmiller, Anthony A1 Wang, Shuo A1 Huang, Kenneth A1 Brown, Edward M. A1 Moremen, Kelley W. A1 Hu, Jian A1 Yang, Jenny J. YR 2016 UL http://advances.sciencemag.org/content/2/5/e1600241.abstract AB Ca2+-sensing receptors (CaSRs) modulate calcium and magnesium homeostasis and many (patho)physiological processes by responding to extracellular stimuli, including divalent cations and amino acids. We report the first crystal structure of the extracellular domain (ECD) of human CaSR bound with Mg2+ and a tryptophan derivative ligand at 2.1 Å. The structure reveals key determinants for cooperative activation by metal ions and aromatic amino acids. The unexpected tryptophan derivative was bound in the hinge region between two globular ECD subdomains, and represents a novel high-affinity co-agonist of CaSR. The dissection of structure-function relations by mutagenesis, biochemical, and functional studies provides insights into the molecular basis of human diseases arising from CaSR mutations. The data also provide a novel paradigm for understanding the mechanism of CaSR-mediated signaling that is likely shared by the other family C GPCR [G protein (heterotrimeric guanine nucleotide–binding protein)–coupled receptor] members and can facilitate the development of novel CaSR-based therapeutics.