biostudies-literature00380Unknown7(1)Mitronova GYVisualization of the G-protein coupled receptor (GPCR) is of great importance for studying its function in a native cell. We have synthesized a series of red-emitting fluorescent probes targeting β-adrenergic receptor (βAR) that are compatible with confocal and Stimulated Emission Depletion (STED) microscopy as well as with Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) binding assay in living cells. The probe based on the agonist BI-167107 and fluorescent dye KK114 demonstrates nanomolar binding affinity and up to nine-fold β₂AR selectivity over β₁AR. Carazolol-derived probes are fluorogenic and allow no-wash imaging experiments. STED microscopy of β₂ARs stained at the native expression level on pancreatic CAPAN cells provides two-fold improvement in lateral optical resolution over confocal mode and reveals the formation of receptor microdomains. These probes retain their functional (agonist or antagonist) properties, allowing simultaneous modulation of cyclic adenosine monophosphate (cAMP) levels and receptor internalization as well as imaging receptor localization.Scientific reports12319https://www.ebi.ac.uk/biostudies/studies/S-EPMC5614969biostudies-literatureHigh-Affinity Functional Fluorescent Ligands for Human β-Adrenoceptors.PMC5614969Mitronova GYLukinavicius GButkevich ANKohl TBelov VNLehnart SEHell SW38falseHigh-Affinity Functional Fluorescent Ligands for Human β-Adrenoceptors.Visualization of the G-protein coupled receptor (GPCR) is of great importance for studying its function in a native cell. We have synthesized a series of red-emitting fluorescent probes targeting β-adrenergic receptor (βAR) that are compatible with confocal and Stimulated Emission Depletion (STED) microscopy as well as with Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) binding assay in living cells. The probe based on the agonist BI-167107 and fluorescent dye KK114 demonstrates nanomolar binding affinity and up to nine-fold β₂AR selectivity over β₁AR. Carazolol-derived probes are fluorogenic and allow no-wash imaging experiments. STED microscopy of β₂ARs stained at the native expression level on pancreatic CAPAN cells provides two-fold improvement in lateral optical resolution over confocal mode and reveals the formation of receptor microdomains. These probes retain their functional (agonist or antagonist) properties, allowing simultaneous modulation of cyclic adenosine monophosphate (cAMP) levels and receptor internalization as well as imaging receptor localization.2017-01-01T00:00:00Z2017 Sep2024-10-18T04:26:14.359Z2019-03-27T02:57:25ZS-EPMC56149692895155810.1038/s41598-017-12468-3