Cell-based and isoform-selective G protein-coupled receptor kinase assays for comprehensive inhibitor evaluation

G protein-coupled receptor (GPCR) signaling is regulated by four ubiquitously expressed GPCR kinase isoforms (GRKs), namely GRK2, GRK3, GRK5, and GRK6. Overexpression of individual GRKs occurs in diseases like cancer and heart failure, prompting a search for potent GRK inhibitors. While various in silico and in vitro approaches exist, few methods assess inhibitor efficacy in cellular systems. To address this, we used HEK293 cell lines co-expressing the β2 adrenergic receptor (β2) and one GRK isoform on a quadruple GRK2/3/5/6 knockout background (ΔQ-GRK). We evaluated the inhibition of isoproterenol (ISO)-induced T360/S364-β2 phosphorylation using the 7TM phosphorylation assay. This combination allowed comprehensive evaluation of commercially available GRK inhibitors. We conclude that compound 8h (GRK2/3 inhibitor) and compound 18 (GRK5/6 inhibitor) are highly recommendable tools for the study of GPCR phosphorylation and function in cellular systems. Together, these cell-based GRK inhibitor assays can facilitate medium- to high-throughput screening of future GRK-targeted drug candidates.

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Journal
Communications Biology
Published
2026-01-16
DOI
https://doi.org/10.1038/s42003-026-09568-0
Primary Topic
Receptor Mechanisms and Signaling
Type
article
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article

Cell-based and isoform-selective G protein-coupled receptor kinase assays for comprehensive inhibitor evaluation

Laura Klement, David Uehling, Falko Nagel, Nina Kathleen Blum et al.
Communications Biology
Receptor Mechanisms and Signaling
article

Cell-based and isoform-selective G protein-coupled receptor kinase assays for comprehensive inhibitor evaluation

Laura Klement, David Uehling, Falko Nagel, Nina Kathleen Blum, Babu Joseph, Verena Weizel, Edda SF Matthees, Julia Drube, Angelika Decker, Carsten Hoffmann, Manuela C. Kiefer
article en

Abstract

G protein-coupled receptor (GPCR) signaling is regulated by four ubiquitously expressed GPCR kinase isoforms (GRKs), namely GRK2, GRK3, GRK5, and GRK6. Overexpression of individual GRKs occurs in diseases like cancer and heart failure, prompting a search for potent GRK inhibitors. While various in silico and in vitro approaches exist, few methods assess inhibitor efficacy in cellular systems. To address this, we used HEK293 cell lines co-expressing the β2 adrenergic receptor (β2) and one GRK isoform on a quadruple GRK2/3/5/6 knockout background (ΔQ-GRK). We evaluated the inhibition of isoproterenol (ISO)-induced T360/S364-β2 phosphorylation using the 7TM phosphorylation assay. This combination allowed comprehensive evaluation of commercially available GRK inhibitors. We conclude that compound 8h (GRK2/3 inhibitor) and compound 18 (GRK5/6 inhibitor) are highly recommendable tools for the study of GPCR phosphorylation and function in cellular systems. Together, these cell-based GRK inhibitor assays can facilitate medium- to high-throughput screening of future GRK-targeted drug candidates.

Communications BiologyVol. 9(1)
Ontario Institute for Cancer Research (CA), Institute of Molecular Biotechnology (AT), Helmholtz Institute Jena (DE), Jena University Hospital (DE), Friedrich Schiller University Jena (DE)
Good health and well-being
Openalex Percentile: Top 87%
Receptor Mechanisms and Signaling
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Cell-based and isoform-selective G protein-coupled receptor kinase assays for comprehensive inhibitor evaluation — Laura Klement, David Uehling, et al. · Communications Biology (2026) | TGRS Research Map | TGRS