A novel enzyme complementation-based assay for monitoring G-protein-coupled receptor internalization

G-protein-coupled receptor ( GPCR) signaling is involved in a wide range of physiological processes and diseases, and around one- half of currently used drugs target GPCRs. Assays for the signaling of GPCRs have suffered from drawbacks, including low signal- to- noise, temporally transient signals, and difficulty in applying a single assay to a wide range of GPCRs. We have developed a set of assays for G-protein-coupled receptor signaling based on beta-galactosidase enzyme complementation in live mammalian cells. We previously described an assay for GPCR activation by monitoring the binding of beta-arrestin to the receptor. Here we describe a second assay that monitors the internalization of GPCRs to endosomes, an event that follows receptor activation and is critical in desensitizing and resensitizing the receptor. We show that both assays display high signal- to- noise ratios with low variability and are quantitative for a wide range of GPCRs. EC(50)s obtained with these assays closely match results reported in the literature. Finally, we show that these assays are readily adapted to high- throughput chemical screens. Thus, these two assays for monitoring G- protein- coupled receptor activation and internalization should prove valuable in basic biological studies as well as in high- throughput screens.