Functional effects of monoclonal antibodies to the purified amino-terminal extracellular domain of the human Ca2+ receptor

Jianxin Hu, Guadalupe Reyes-Cruz, Paul K. Goldsmith, Nicole M. Gantt, Jeffery L. Miller, Allen M. Spiegel

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

We generated three functionally unique monoclonal antibodies to the purified human CaR extracellular domain. Flow cytometry studies of chimeric receptors localized their epitopes to lobe 2 of the VFT domain. These results lead us to propose a mechanism for the functional effects of these antibodies. Introduction: The human Ca2+ receptor (CaR), which plays a central role in the regulation of [Ca2+]0 homeostasis, has a distinctively large extracellular domain that consists of a bilobed Venus flytrap (VFT) domain, involved in agonist binding, and a cysteine-rich domain. Functional antibodies that specifically bind to this domain would have therapeutic potential and could be used as a tool to gain insights into receptor activation as well. Materials and Methods: We generated three monoclonal antibodies (mAbs), 7F8, 5C8, and 1A8, to the purified human CaR extracellular domain. Functional characterization of these antibodies included Ca2+ stimulation of phosphoinositide hydrolysis to examine effects of intact or protease digested antibodies on sensitivity of the receptor to extracellular Ca2+ and flow cytometry assay of binding of the antibodies to HEK-293 cells expressing chimeric receptors to map antibody epitopes. Results: We found these mAbs specifically recognize native but not denatured human CaR or homologous native Fugu CaR. Sensitivity of the human CaR to extracellular calcium was increased by binding of 5C8 but decreased by binding of 1A8. A chimeric receptor FCFCF, with lobe 2 region of the human CaR VFT domain in the Fugu CaR backbone, bound all three mAbs, and the sensitivity of this chimeric CaR to extracellular Ca2+ was also increased by binding of 5C8 and decreased by binding of 1A8. Conclusions: The epitopes of these mAbs reside in the lobe 2 region of the human CaR VFT domain. 5C8 might activate the receptor by facilitating closure and/or rotation of the VFT domains on agonist binding, whereas 1A8 might inhibit the receptor by impeding such agonist-induced conformational changes. Recombinant antibodies with antigen binding domains of 5C8 and 1A8 could be useful in the treatment of hyperparathyroidism and osteoporosis, respectively.

Original languageEnglish (US)
Pages (from-to)601-608
Number of pages8
JournalJournal of Bone and Mineral Research
Volume22
Issue number4
DOIs
StatePublished - Apr 2007
Externally publishedYes

Fingerprint

Droseraceae
Monoclonal Antibodies
Antibodies
Takifugu
Epitopes
Flow Cytometry
Hyperparathyroidism
HEK293 Cells
Phosphatidylinositols
Osteoporosis
Cysteine
Hydrolysis
Homeostasis
Peptide Hydrolases
Calcium
Antigens

Keywords

  • Chimeric receptor
  • Extracellular domain
  • Human Ca receptor
  • Monoclonal antibodies
  • Venus flytrap-like domain

ASJC Scopus subject areas

  • Surgery

Cite this

Functional effects of monoclonal antibodies to the purified amino-terminal extracellular domain of the human Ca2+ receptor. / Hu, Jianxin; Reyes-Cruz, Guadalupe; Goldsmith, Paul K.; Gantt, Nicole M.; Miller, Jeffery L.; Spiegel, Allen M.

In: Journal of Bone and Mineral Research, Vol. 22, No. 4, 04.2007, p. 601-608.

Research output: Contribution to journalArticle

Hu, Jianxin ; Reyes-Cruz, Guadalupe ; Goldsmith, Paul K. ; Gantt, Nicole M. ; Miller, Jeffery L. ; Spiegel, Allen M. / Functional effects of monoclonal antibodies to the purified amino-terminal extracellular domain of the human Ca2+ receptor. In: Journal of Bone and Mineral Research. 2007 ; Vol. 22, No. 4. pp. 601-608.
@article{ef1059be5a4347a8837e068522ed41cf,
title = "Functional effects of monoclonal antibodies to the purified amino-terminal extracellular domain of the human Ca2+ receptor",
abstract = "We generated three functionally unique monoclonal antibodies to the purified human CaR extracellular domain. Flow cytometry studies of chimeric receptors localized their epitopes to lobe 2 of the VFT domain. These results lead us to propose a mechanism for the functional effects of these antibodies. Introduction: The human Ca2+ receptor (CaR), which plays a central role in the regulation of [Ca2+]0 homeostasis, has a distinctively large extracellular domain that consists of a bilobed Venus flytrap (VFT) domain, involved in agonist binding, and a cysteine-rich domain. Functional antibodies that specifically bind to this domain would have therapeutic potential and could be used as a tool to gain insights into receptor activation as well. Materials and Methods: We generated three monoclonal antibodies (mAbs), 7F8, 5C8, and 1A8, to the purified human CaR extracellular domain. Functional characterization of these antibodies included Ca2+ stimulation of phosphoinositide hydrolysis to examine effects of intact or protease digested antibodies on sensitivity of the receptor to extracellular Ca2+ and flow cytometry assay of binding of the antibodies to HEK-293 cells expressing chimeric receptors to map antibody epitopes. Results: We found these mAbs specifically recognize native but not denatured human CaR or homologous native Fugu CaR. Sensitivity of the human CaR to extracellular calcium was increased by binding of 5C8 but decreased by binding of 1A8. A chimeric receptor FCFCF, with lobe 2 region of the human CaR VFT domain in the Fugu CaR backbone, bound all three mAbs, and the sensitivity of this chimeric CaR to extracellular Ca2+ was also increased by binding of 5C8 and decreased by binding of 1A8. Conclusions: The epitopes of these mAbs reside in the lobe 2 region of the human CaR VFT domain. 5C8 might activate the receptor by facilitating closure and/or rotation of the VFT domains on agonist binding, whereas 1A8 might inhibit the receptor by impeding such agonist-induced conformational changes. Recombinant antibodies with antigen binding domains of 5C8 and 1A8 could be useful in the treatment of hyperparathyroidism and osteoporosis, respectively.",
keywords = "Chimeric receptor, Extracellular domain, Human Ca receptor, Monoclonal antibodies, Venus flytrap-like domain",
author = "Jianxin Hu and Guadalupe Reyes-Cruz and Goldsmith, {Paul K.} and Gantt, {Nicole M.} and Miller, {Jeffery L.} and Spiegel, {Allen M.}",
year = "2007",
month = "4",
doi = "10.1359/jbmr.070111",
language = "English (US)",
volume = "22",
pages = "601--608",
journal = "Journal of Bone and Mineral Research",
issn = "0884-0431",
publisher = "Wiley-Blackwell",
number = "4",

}

TY - JOUR

T1 - Functional effects of monoclonal antibodies to the purified amino-terminal extracellular domain of the human Ca2+ receptor

AU - Hu, Jianxin

AU - Reyes-Cruz, Guadalupe

AU - Goldsmith, Paul K.

AU - Gantt, Nicole M.

AU - Miller, Jeffery L.

AU - Spiegel, Allen M.

PY - 2007/4

Y1 - 2007/4

N2 - We generated three functionally unique monoclonal antibodies to the purified human CaR extracellular domain. Flow cytometry studies of chimeric receptors localized their epitopes to lobe 2 of the VFT domain. These results lead us to propose a mechanism for the functional effects of these antibodies. Introduction: The human Ca2+ receptor (CaR), which plays a central role in the regulation of [Ca2+]0 homeostasis, has a distinctively large extracellular domain that consists of a bilobed Venus flytrap (VFT) domain, involved in agonist binding, and a cysteine-rich domain. Functional antibodies that specifically bind to this domain would have therapeutic potential and could be used as a tool to gain insights into receptor activation as well. Materials and Methods: We generated three monoclonal antibodies (mAbs), 7F8, 5C8, and 1A8, to the purified human CaR extracellular domain. Functional characterization of these antibodies included Ca2+ stimulation of phosphoinositide hydrolysis to examine effects of intact or protease digested antibodies on sensitivity of the receptor to extracellular Ca2+ and flow cytometry assay of binding of the antibodies to HEK-293 cells expressing chimeric receptors to map antibody epitopes. Results: We found these mAbs specifically recognize native but not denatured human CaR or homologous native Fugu CaR. Sensitivity of the human CaR to extracellular calcium was increased by binding of 5C8 but decreased by binding of 1A8. A chimeric receptor FCFCF, with lobe 2 region of the human CaR VFT domain in the Fugu CaR backbone, bound all three mAbs, and the sensitivity of this chimeric CaR to extracellular Ca2+ was also increased by binding of 5C8 and decreased by binding of 1A8. Conclusions: The epitopes of these mAbs reside in the lobe 2 region of the human CaR VFT domain. 5C8 might activate the receptor by facilitating closure and/or rotation of the VFT domains on agonist binding, whereas 1A8 might inhibit the receptor by impeding such agonist-induced conformational changes. Recombinant antibodies with antigen binding domains of 5C8 and 1A8 could be useful in the treatment of hyperparathyroidism and osteoporosis, respectively.

AB - We generated three functionally unique monoclonal antibodies to the purified human CaR extracellular domain. Flow cytometry studies of chimeric receptors localized their epitopes to lobe 2 of the VFT domain. These results lead us to propose a mechanism for the functional effects of these antibodies. Introduction: The human Ca2+ receptor (CaR), which plays a central role in the regulation of [Ca2+]0 homeostasis, has a distinctively large extracellular domain that consists of a bilobed Venus flytrap (VFT) domain, involved in agonist binding, and a cysteine-rich domain. Functional antibodies that specifically bind to this domain would have therapeutic potential and could be used as a tool to gain insights into receptor activation as well. Materials and Methods: We generated three monoclonal antibodies (mAbs), 7F8, 5C8, and 1A8, to the purified human CaR extracellular domain. Functional characterization of these antibodies included Ca2+ stimulation of phosphoinositide hydrolysis to examine effects of intact or protease digested antibodies on sensitivity of the receptor to extracellular Ca2+ and flow cytometry assay of binding of the antibodies to HEK-293 cells expressing chimeric receptors to map antibody epitopes. Results: We found these mAbs specifically recognize native but not denatured human CaR or homologous native Fugu CaR. Sensitivity of the human CaR to extracellular calcium was increased by binding of 5C8 but decreased by binding of 1A8. A chimeric receptor FCFCF, with lobe 2 region of the human CaR VFT domain in the Fugu CaR backbone, bound all three mAbs, and the sensitivity of this chimeric CaR to extracellular Ca2+ was also increased by binding of 5C8 and decreased by binding of 1A8. Conclusions: The epitopes of these mAbs reside in the lobe 2 region of the human CaR VFT domain. 5C8 might activate the receptor by facilitating closure and/or rotation of the VFT domains on agonist binding, whereas 1A8 might inhibit the receptor by impeding such agonist-induced conformational changes. Recombinant antibodies with antigen binding domains of 5C8 and 1A8 could be useful in the treatment of hyperparathyroidism and osteoporosis, respectively.

KW - Chimeric receptor

KW - Extracellular domain

KW - Human Ca receptor

KW - Monoclonal antibodies

KW - Venus flytrap-like domain

UR - http://www.scopus.com/inward/record.url?scp=34249718528&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=34249718528&partnerID=8YFLogxK

U2 - 10.1359/jbmr.070111

DO - 10.1359/jbmr.070111

M3 - Article

VL - 22

SP - 601

EP - 608

JO - Journal of Bone and Mineral Research

JF - Journal of Bone and Mineral Research

SN - 0884-0431

IS - 4

ER -