| Literature DB >> 28570808 |
Anders Højgaard Hansen1, Eugenia Sergeev2, Sunil K Pandey1, Brian D Hudson2, Elisabeth Christiansen1, Graeme Milligan2, Trond Ulven1.
Abstract
The free fatty acid receptor 2 (FFA2/GPR43) is considered a potential target for treatment of metabolic and inflammatory diseases. Here we describe the development of the first fluorescent tracer for FFA2 intended as a tool for assessment of thermodynamic and kinetic binding parameters of unlabeled ligands. Starting with a known azetidine FFA2 antagonist, we used a carboxylic acid moiety known not to be critical for receptor interaction as attachment point for a nitrobenzoxadiazole (NBD) fluorophore. This led to the development of 4 (TUG-1609), a fluorescent tracer for FFA2 with favorable spectroscopic properties and high affinity, as determined by bioluminescence resonance energy transfer (BRET)-based saturation and kinetic binding experiments, as well as a high specific to nonspecific BRET binding signal. A BRET-based competition binding assay with 4 was also established and used to determine binding constants and kinetics of unlabeled ligands.Entities:
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Year: 2017 PMID: 28570808 DOI: 10.1021/acs.jmedchem.7b00338
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446