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A novel and selective fluorescent ligand for the study of adenosine A2B receptors

Patera, Foteini; Mistry, Sarah J.; Kindon, Nicholas D.; Comeo, Eleonora; Gouding, Joelle; Kellam, Barrie; Kilpatrick, Laura E.; Franks, Hester; Hill, Stephen J.

A novel and selective fluorescent ligand for the study of adenosine A2B receptors Thumbnail


Authors

Foteini Patera

Sarah J. Mistry

Eleonora Comeo

Profile image of BARRIE KELLAM

BARRIE KELLAM BARRIE.KELLAM@NOTTINGHAM.AC.UK
Professor of Medicinal Chemistry

HESTER FRANKS HESTER.FRANKS@NOTTINGHAM.AC.UK
Clinical Associate Professor/ anne Mclaren Fellowship

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 characterised 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 tumour 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 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 tumour microenvironment.

Citation

Patera, F., Mistry, S. J., Kindon, N. D., Comeo, E., Gouding, 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 2024-08
Deposit Date Jun 13, 2024
Publicly Available Date Jun 13, 2024
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
Keywords Adenosine A2B receptor; fluorescent ligand; macrophages; ligand-binding; PSB603; antagonist
Public URL https://nottingham-repository.worktribe.com/output/36011523
Publisher URL https://bpspubs.onlinelibrary.wiley.com/doi/10.1002/prp2.1223