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ThermoBRET: A Ligand-Engagement Nanoscale Thermostability Assay Applied to GPCRs**

Hoare, Bradley L.; Tippett, David N.; Kaur, Amandeep; Cullum, Sean A.; Miljuš, Tamara; Koers, Eline J.; Harwood, Clare R.; Dijon, Nicola; Holliday, Nicholas D.; Sykes, David A.; Veprintsev, Dmitry B.

ThermoBRET: A Ligand-Engagement Nanoscale Thermostability Assay Applied to GPCRs** Thumbnail


Authors

Bradley L. Hoare

David N. Tippett

Amandeep Kaur

Sean A. Cullum

Tamara Miljuš

Clare R. Harwood

Nicola Dijon

David A. Sykes

DMITRY VEPRINTSEV DMITRY.VEPRINTSEV@NOTTINGHAM.AC.UK
Professor of Molecular and Cellular Pharmacology



Abstract

Measurements of membrane protein thermostability reflect ligand binding. Current thermostability assays often require protein purification or rely on pre-existing radiolabelled or fluorescent ligands, limiting their application to established targets. Alternative methods, such as fluorescence-detection size exclusion chromatography thermal shift, detect protein aggregation but are not amenable to high-throughput screening. Here, we present a ThermoBRET method to quantify the relative thermostability of G protein coupled receptors (GPCRs), using cannabinoid receptors (CB1 and CB2) and the β2-adrenoceptor (β2AR) as model systems. ThermoBRET reports receptor unfolding, does not need labelled ligands and can be used with non-purified proteins. It uses Bioluminescence Resonance Energy Transfer (BRET) between Nanoluciferase (Nluc) and a thiol-reactive fluorescent dye that binds cysteines exposed by unfolding. We demonstrate that the melting point (Tm) of Nluc-fused GPCRs can be determined in non-purified detergent solubilised membrane preparations or solubilised whole cells, revealing differences in thermostability for different solubilising conditions and in the presence of stabilising ligands. We extended the range of the assay by developing the thermostable tsNLuc by incorporating mutations from the fragments of split-Nluc (Tm of 87 °C versus 59 °C). ThermoBRET allows the determination of GPCR thermostability, which is useful for protein purification optimisation and drug discovery screening.

Citation

Hoare, B. L., Tippett, D. N., Kaur, A., Cullum, S. A., Miljuš, T., Koers, E. J., …Veprintsev, D. B. (2024). ThermoBRET: A Ligand-Engagement Nanoscale Thermostability Assay Applied to GPCRs**. ChemBioChem, 25(2), Article e202300459. https://doi.org/10.1002/cbic.202300459

Journal Article Type Article
Acceptance Date Oct 23, 2023
Online Publication Date Nov 28, 2023
Publication Date Jan 15, 2024
Deposit Date Nov 20, 2023
Publicly Available Date Oct 24, 2024
Journal ChemBioChem
Print ISSN 1439-4227
Electronic ISSN 1439-7633
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 25
Issue 2
Article Number e202300459
DOI https://doi.org/10.1002/cbic.202300459
Keywords GPCR, membrane protein stability, thermal shift, ligand binding, detergent solubilisation, thermostability, thermal shift assay, nanoBRET
Public URL https://nottingham-repository.worktribe.com/output/27069687
Publisher URL https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cbic.202300459

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