Consider Eurofins DiscoverX’s custom development capabilities for custom cell lines, assays, & enzyme development.
GPCR internalization is essential to prevent cells from undergoing excessive receptor stimulation or periods of prolonged inactivity. If GPCR internalization is inhibited by a ligand, a protein mutation, or aberrant signaling, undesirable effects may occur, often resulting in drug tolerance, unwanted side effects, and disease.
PathHunter® GPCR internalization assays from Eurofins DiscoverX® are functional, cell-based assays that measure GPCR endocytosis. These non-imaging, non-antibody-based, mechanism of action (MOA)-reflective chemiluminescent cellular assays directly and quantitatively measure internalized GPCRs localized to intracellular endosomes. This allows the fate of activated GPCRs to be monitored in live cells without requiring expensive microscopy.
Consider Eurofins DiscoverX’s custom development capabilities for custom cell lines, assays, & enzyme development.
PathHunter GPCR internalization assays are based on the proprietary Enzyme Fragment Complementation (EFC) technology and provide a tool for secondary or orthogonal screening to identify safer drugs with less undesirable effects like drug tolerance, unwanted side effects, and disease. There are two assay formats for detecting receptor internalization in whole cells. The total internalization assay detects ligand-induced GPCR endocytosis via all endocytosis mechanisms; the activated internalization assay looks at only ligand-induced, β-arrestin-mediated receptor internalization.
PathHunter total GPCR internalization assay principle. Cell lines are engineered to co-express two fragments of the β-galactosidase (β-gal) enzyme – a small EFC enzyme donor (ED) and a larger EFC enzyme acceptor (EA). In A., the ED is tagged to the GPCR, and the EA is localized to the endosome. In B., the ED is localized to the endosome, and the EA tagged to the GPCR. In both formats, small molecule or biologic (e.g. antibody) ligands that bind the GPCR-tagged fusion protein leads to internalization (endocytosis) of the receptor to the endosome, forcing the complementation of the two β-gal enzyme fragments (ED and EA). The resulting functional β-gal enzyme hydrolyzes a substrate to generate a dose-dependent chemiluminescent signal.
PathHunter activated GPCR internalization assay principle. Cell lines are engineered to co-express an untagged GPCR, an EA tagged β-arrestin, and an ED tag localized to the endosomes. Activation of the untagged GPCR induces β-arrestin recruitment, followed by internalization of the GPCR-β-arrestin-EA complex to the ED-tagged endosomes. Similar to the total assay format, this internalization forces the complementation of the two β-gal enzyme fragments, forming a functional enzyme that hydrolyzes substrate to generate a chemiluminescent signal.