Foteini Patera
A novel and selective fluorescent ligand for the study of adenosine A2B receptors
Patera, Foteini; Mistry, Sarah J.; Kindon, Nicholas D.; Comeo, Eleonora; Goulding, Joelle; Kellam, Barrie; Kilpatrick, Laura E.; Franks, Hester; Hill, Stephen J.
Authors
Sarah J. Mistry
Dr NICHOLAS KINDON Nicholas.Kindon@nottingham.ac.uk
SENIOR RESEARCH FELLOW
Eleonora Comeo
Dr JOELLE GOULDING JOELLE.GOULDING@NOTTINGHAM.AC.UK
SENIOR RESEARCH FELLOW
Professor BARRIE KELLAM BARRIE.KELLAM@NOTTINGHAM.AC.UK
Head of School (Professor of Medicinal Chemistry)
Dr LAURA KILPATRICK LAURA.KILPATRICK@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR
Dr HESTER FRANKS HESTER.FRANKS@NOTTINGHAM.AC.UK
CLINICAL ASSOCIATE PROFESSOR/ ANNE MCLAREN FELLOWSHIP
Professor STEPHEN HILL STEVE.HILL@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR PHARMACOLOGY
Abstract
Fluorescent ligands have proved to be powerful tools in the study of G protein-coupled receptors in living cells. Here we have characterized a new fluorescent ligand PSB603-BY630 that has high selectivity for the human adenosine A2B receptor (A2BR). The A2BR appears to play an important role in regulating immune responses in the tumor microenvironment. Here we have used PSB603-BY630 to monitor specific binding to A2BRs in M1- and M2-like macrophages derived from CD14+ human monocytes. PSB603-BY630 bound with high affinity (18.3 nM) to nanoluciferase-tagged A2BRs stably expressed in HEK293G cells. The ligand exhibited very high selectivity for the A2BR with negligible specific-binding detected at NLuc-A2AR, NLuc-A1R, or NLuc-A3R receptors at concentrations up to 500 nM. Competition binding studies showed the expected pharmacology at A2BR with the A2BR-selective ligands PSB603 and MRS-1706 demonstrating potent inhibition of the specific binding of 50 nM PSB603-BY630 to A2BR. Functional studies in HEK293G cells using Glosensor to monitor Gs-coupled cyclic AMP responses indicated that PSB603-BY630 acted as a negative allosteric regular of the agonist responses to BAY 60–6583. Furthermore, flow cytometry analysis confirmed that PSB603-BY630 could be used to selectively label endogenous A2BRs expressed on human macrophages. This ligand should be an important addition to the library of fluorescent ligands which are selective for the different adenosine receptor subtypes, and will enable study of the role of A2BRs on immune cells in the tumor microenvironment.
Citation
Patera, F., Mistry, S. J., Kindon, N. D., Comeo, E., Goulding, J., Kellam, B., Kilpatrick, L. E., Franks, H., & Hill, S. J. (2024). A novel and selective fluorescent ligand for the study of adenosine A2B receptors. Pharmacology Research and Perspectives, 12(4), Article e1223. https://doi.org/10.1002/prp2.1223
Journal Article Type | Article |
---|---|
Acceptance Date | May 27, 2024 |
Online Publication Date | Jun 21, 2024 |
Publication Date | Jun 21, 2024 |
Deposit Date | Feb 24, 2025 |
Publicly Available Date | Feb 26, 2025 |
Journal | Pharmacology Research and Perspectives |
Electronic ISSN | 2052-1707 |
Publisher | Wiley Open Access |
Peer Reviewed | Peer Reviewed |
Volume | 12 |
Issue | 4 |
Article Number | e1223 |
DOI | https://doi.org/10.1002/prp2.1223 |
Public URL | https://nottingham-repository.worktribe.com/output/36580296 |
Publisher URL | https://bpspubs.onlinelibrary.wiley.com/doi/10.1002/prp2.1223 |
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Copyright Statement
© 2024 The Author(s). Pharmacology Research & Perspectives published by British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics and John Wiley & Sons Ltd.
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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