Parathyroid Hormone Senses Extracellular Calcium To Modulate Endocrine Signaling upon Binding to the Family B GPCR Parathyroid Hormone 1 Receptor

被引:6
作者
Culhane, Kelly J. [1 ]
Belina, Morgan E.
Sims, Jeremiah N. [3 ]
Cai, Yingying
Liu, Yuting
Wang, Pam S. P. [4 ]
Yan, Elsa C. Y. [2 ]
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, 266 Whitney Ave, New Haven, CT 06520 USA
[2] Yale Univ, Dept Chem, 225 Prospect St, New Haven, CT 06520 USA
[3] NIAID, Lab Malaria & Vector Res, NIH, Bethesda, MD 20892 USA
[4] Moderna Therapeut, 320 Bent St, Cambridge, MA 02141 USA
关键词
PROTEIN-COUPLED RECEPTOR; HIGH-LEVEL EXPRESSION; LARGE-SCALE PURIFICATION; BIOPHYSICAL CHARACTERIZATION; JUXTAMEMBRANE REGION; LIGAND-BINDING; PTH RECEPTOR; CELL-LINES; BONE; ACTIVATION;
D O I
10.1021/acschembio.8b00568
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Parathyroid hormone (PTH) binds to a family B G protein coupled receptor, parathyroid hormone 1 receptor (PTH1R). One of its functions is to regulate Ca2+ homeostasis in bone remodeling, during which Ca2+ can reach up to 40 mM. A truncated version of PTH, PTH(1-34), can fully activate PTH1R and has been used for osteoporosis treatments. Here, we used fluorescence anisotropy to examine the binding of PTH(1-34) to PTH1R purified in nanodiscs (PTH1R-ND) and found that the affinity increases 5-fold in the presence of 15 mM Ca2+. However, PTHrP(1-36), another truncated endogenous agonist for PTH1R, does not show this Ca2+ effect. Mutations of Glu19 and Glu22 in PTH(1-34) that are not conserved in PTHrP(1-36) largely abolished the Ca2+ effect. The results support that PTH(1-34) not only activates PTH1R but also uniquely senses Ca2+. This dual function of a peptide hormone is a novel observation that couples changes in extracellular environment with endocrine signaling. Understanding this can potentially reveal the complex role of PTH signaling in bone remodeling and improve the PTH(1-34) treatment for osteoporosis.
引用
收藏
页码:2347 / 2358
页数:12
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