Author:
Kaufmann Johanna,Blum Nina Kathleen,Nagel Falko,Schuler Anna,Drube Julia,Degenhart Carsten,Engel Julian,Eickhoff Jan Eicke,Dasgupta Pooja,Fritzwanker Sebastian,Guastadisegni Maria,Schulte Clemens,Miess-Tanneberg Elke,Maric Hans Michael,Spetea Mariana,Kliewer Andrea,Baumann Matthias,Klebl Bert,Reinscheid Rainer K.,Hoffmann Carsten,Schulz Stefan
Abstract
AbstractAnalysis of agonist-driven phosphorylation of G protein-coupled receptors (GPCRs) can provide valuable insights into the receptor activation state and ligand pharmacology. However, to date, assessment of GPCR phosphorylation using high-throughput applications has been challenging. We have developed and validated a bead-based immunoassay for the quantitative assessment of agonist-induced GPCR phosphorylation that can be performed entirely in multiwell cell culture plates. The assay involves immunoprecipitation of affinity-tagged receptors using magnetic beads followed by protein detection using phosphorylation-state-specific and phosphorylation state-independent anti-GPCR antibodies. As proof of concept, five prototypical GPCRs (MOP, C5a1, D1, SST2, CB2) were treated with different agonists and antagonists, and concentration-response curves were generated. We then extended our approach to establish selective cellular GPCR kinase (GRK) inhibitor assays, which led to the rapid identification of a selective GRK5/6 inhibitor (LDC8988) and a highly potent pan-GRK inhibitor (LDC9728). In conclusion, this versatile GPCR phosphorylation assay can be used extensively for ligand profiling and inhibitor screening.
Publisher
Cold Spring Harbor Laboratory