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.