Catherine J. Hutchings
Monoclonal anti-β1-adrenergic receptor antibodies activate G protein signaling in the absence of β-arrestin recruitment
Hutchings, Catherine J.; Cseke, Gabriella; Osborne, Greg; Woolard, Jeanette; Zhukov, Andrei; Koglin, Markus; Jazayeri, Ali; Pandya-Pathak, Jahnavi; Langmead, Christopher J.; Hill, Stephen J.; Weir, Malcolm; Marshall, Fiona H.
Authors
Gabriella Cseke
Greg Osborne
JEANETTE WOOLARD Jeanette.Woolard@nottingham.ac.uk
Professor of Cardiovascular Physiology and Pharmacology
Andrei Zhukov
Markus Koglin
Ali Jazayeri
Jahnavi Pandya-Pathak
Christopher J. Langmead
STEPHEN HILL STEVE.HILL@NOTTINGHAM.AC.UK
Professor of Molecular Pharmacology
Malcolm Weir
Fiona H. Marshall
Abstract
Thermostabilized G protein-coupled receptors used as antigens for in vivo immunization have resulted in the generation of functional agonistic anti-β1-adrenergic (β1AR) receptor monoclonal antibodies (mAbs). The focus of this study was to examine the pharmacology of these antibodies to evaluate their mechanistic activity at β1AR. Immunization with the β1AR stabilized receptor yielded five stable hybridoma clones, four of which expressed functional IgG, as determined in cell-based assays used to evaluate cAMP stimulation. The antibodies bind diverse epitopes associated with low nanomolar agonist activity at β1AR, and they appeared to show some degree of biased signaling as they were inactive in an assay measuring signaling through β-arrestin. In vitro characterization also verified different antibody-receptor interactions reflecting the different epitopes on the extracellular surface of β1AR to which the mAbs bind. The anti-β1AR mAbs only demonstrated agonist activity when in dimeric antibody format, but not as the monomeric Fab format, suggesting that agonist activation may be mediated through promoting receptor dimerization. Finally, we have also shown that at least one of these antibodies exhibits in vivo functional activity at a therapeutically-relevant dose producing an increase in heart rate consistent with β1AR agonism.
Citation
Hutchings, C. J., Cseke, G., Osborne, G., Woolard, J., Zhukov, A., Koglin, M., …Marshall, F. H. (2014). Monoclonal anti-β1-adrenergic receptor antibodies activate G protein signaling in the absence of β-arrestin recruitment. mAbs, 6(1), 246-261. https://doi.org/10.4161/mabs.27226
Journal Article Type | Article |
---|---|
Acceptance Date | Nov 15, 2013 |
Online Publication Date | Nov 19, 2013 |
Publication Date | 2014-01 |
Deposit Date | Jul 21, 2016 |
Publicly Available Date | Jul 21, 2016 |
Journal | mAbs |
Print ISSN | 1942-0862 |
Electronic ISSN | 1942-0870 |
Publisher | Taylor and Francis |
Peer Reviewed | Peer Reviewed |
Volume | 6 |
Issue | 1 |
Pages | 246-261 |
DOI | https://doi.org/10.4161/mabs.27226 |
Keywords | stabilized receptor, Beta 1 adrenergic receptor, GPCR, extracellular domain, extracellular loop, functional antibody, isoprenaline, propranolol |
Public URL | https://nottingham-repository.worktribe.com/output/719289 |
Publisher URL | http://www.tandfonline.com/doi/abs/10.4161/mabs.27226 |
Contract Date | Jul 21, 2016 |
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://eprints.nottingham.ac.uk/end_user_agreement.pdf
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