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Anal Biochem ; 392(2): 103-9, 2009 Sep 15.
Article in English | MEDLINE | ID: mdl-19464246

ABSTRACT

High-sensitivity, high-throughput, and user-friendly lanthanide-based assays for receptor-ligand interactions provide an attractive alternative to the traditional radioligand displacement assays. In this study, three small-molecule pindolol ligand derivatives were synthesized and their binding properties were tested in a radioligand displacement assay. The ligand derivatives were further labeled with fluorescent europium(III) chelate for beta(2)-adrenergic receptor-ligand binding assay. The europium-labeled pindolol ligands having no spacer (C0) or a 12-carbon spacer (C12) arm bound to the human beta(2)-adrenergic receptors overexpressed in human embryonic kidney HEK293(i) cells. Europium ligand with a 6-carbon spacer arm (C6) showed no binding. Competitive binding assays were developed with the functional labeled ligands. The IC(50) values for beta(2)-adrenergic antagonist propranolol were 60 and 37 nM, the Z' values were 0.51 and 0.77, and the signal-to-background ratios were 5.5 and 16.0 for C0 and C12, respectively. This study shows that functional time-resolved fluorescent assays can be constructed using fluorescent lanthanide chelates conjugated to small-molecule ligands.


Subject(s)
Adrenergic beta-Antagonists/analysis , Adrenergic beta-Antagonists/metabolism , Europium/analysis , Pindolol/metabolism , Receptors, Adrenergic, beta-2/metabolism , Spectrometry, Fluorescence/methods , Adrenergic beta-Antagonists/chemical synthesis , Cell Line , Chelating Agents/analysis , Chelating Agents/chemistry , Chelating Agents/metabolism , Europium/chemistry , Humans , Ligands , Molecular Structure , Pindolol/analogs & derivatives , Pindolol/analysis , Pindolol/chemical synthesis , Receptors, Adrenergic, beta-2/genetics , Time Factors , Transgenes/genetics
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