Title

Role of Ca2+ and L-Phe in Regulating Functional Cooperativity of Disease- Associated ‘‘Toggle’’ Calcium-Sensing Receptor Mutations

Authors

Chen Zhang, Georgia State UniversityFollow
Nagaraju Mulpuri, Georgia State UniversityFollow
Fadil M. Hannan, University of OxfordFollow
M. Andrew Nesbit, University of Oxford
Rajesh V. Thakker, University of OxfordFollow
Donald Hamelberg, Georgia State UniversityFollow
Edward M. Brown, Brigham and Women's Hospital
Jenny J. Yang, Georgia State UniversityFollow

Document Type

Article

Publication Date

11-2014

Abstract

The Ca2+-sensing receptor (CaSR) regulates Ca2+ homeostasis in the body by monitoring extracellular levels of Ca2+ ([Ca2+]o) and amino acids. Mutations at the hinge region of the N-terminal Venus flytrap domain (VFTD) produce either receptor inactivation (L173P, P221Q) or activation (L173F, P221L) related to hypercalcemic or hypocalcemic disorders. In this paper, we report that both L173P and P221Q markedly impair the functional positive cooperativity of the CaSR as reflected by [Ca2+]o–induced [Ca2+]i oscillations, inositol-1-phosphate (IP1) accumulation and extracellular signal-regulated kinases (ERK1/2) activity. In contrast, L173F and P221L show enhanced responsiveness of these three functional readouts to [Ca2+]o. Further analysis of the dynamics of the VFTD mutants using computational simulation studies supports disruption in the correlated motions in the loss-offunction CaSR mutants, while these motions are enhanced in the gain-of-function mutants. Wild type (WT) CaSR was modulated by L-Phe in a heterotropic positive cooperative way, achieving an EC50 similar to those of the two activating mutations. The response of the inactivating P221Q mutant to [Ca2+]o was partially rescued by L-Phe, illustrating the capacity of the L-Phe binding site to enhance the positive homotropic cooperativity of CaSR. L-Phe had no effect on the other inactivating mutant. Moreover, our results carried out both in silico and in intact cells indicate that residue Leu173, which is close to residues that are part of the L-Phe-binding pocket, exhibited impaired heterotropic cooperativity in the presence of L-Phe. Thus, Pro221 and Leu173 are important for the positive homo- and heterotropic cooperative regulation elicited by agonist binding.

Comments

Originally Published in:

PLoS ONE 9(11): e113622. doi:http://dx.doi.org/10.1371/journal.pone.0113622

Recommended Citation

Zhang C, Mulpuri N, Hannan FM, Nesbit MA, Thakker RV, et al. (2014) Role of Ca2+ and LPhe in Regulating Functional Cooperativity of Disease-Associated ‘‘Toggle’’ Calcium-Sensing Receptor Mutations. PLoS ONE 9(11): e113622. doi:http://dx.doi.org/10.1371/journal.pone.0113622

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