BRET- and fluorescence anisotropy-based assays for real-time monitoring of ligand binding to M2 muscarinic acetylcholine receptors
Autor: | Maris-Johanna Tahk, Max Keller, Corinna G. Gruber, Andrea Pegoli, Tõnis Laasfeld, Mari-Liis Tsernant, Lukas Grätz, Ago Rinken, Anni Allikalt |
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Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Chemistry Cell Biology Ligand (biochemistry) Fluorescence Receptor–ligand kinetics 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Muscarinic acetylcholine receptor Radioligand Biophysics Receptor Molecular Biology 030217 neurology & neurosurgery Fluorescence anisotropy G protein-coupled receptor |
Zdroj: | Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1868:118930 |
ISSN: | 0167-4889 |
DOI: | 10.1016/j.bbamcr.2020.118930 |
Popis: | BRET and fluorescence anisotropy (FA) are two fluorescence-based techniques used for the characterization of ligand binding to G protein-coupled receptors (GPCRs) and both allow monitoring of ligand binding in real time. In this study, we present the first direct comparison of BRET-based and FA-based binding assays using the human M2 muscarinic acetylcholine receptor (M2R) and two TAMRA (5-carboxytetramethylrhodamine)-labeled fluorescent ligands as a model system. The determined fluorescent ligand affinities from both assays were in good agreement with results obtained from radioligand competition binding experiments. The assays yielded real-time kinetic binding data revealing differences in the mechanism of binding for the investigated fluorescent probes. Furthermore, the investigation of various unlabeled M2R ligands yielded pharmacological profiles in accordance with earlier reported data. Taken together, this study showed that BRET- and FA-based binding assays represent valuable alternatives to radioactivity-based methods for screening purposes and for a precise characterization of binding kinetics supporting the exploration of binding mechanisms. |
Databáze: | OpenAIRE |
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