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J Biomol Screen ; 16(2): 183-91, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21297105

ABSTRACT

The retinoid acid receptor-related orphan receptors (RORs) represent important targets for the treatment of metabolic and immune disorders. Here the authors describe the application of AlphaScreen(®) technology to develop a high-throughput screening (HTS)-compatible assay to facilitate the discovery of RORα modulators. Using the ligand binding domain (LBD) of RORα and a peptide derived from the NR1 box of the nuclear receptor coactivator PGC-1α, a 384-well format assay was developed exhibiting high sensitivity, requiring only low nanomolar concentration of reagents. Recently, it was shown that oxysterols such as 7α-hydroxycholesterol (7α-OHC) function as modulators of the RORs. In this assay, 7α-OHC produced a concentration-response curve with an EC(50) of 162 nM, a Z' factor of 0.6, and a signal-to-background (S/B) ratio of 4.2, demonstrating that the assay is HTS compatible. Validation of the assay was afforded by screening against the Sigma LOPAC1280™ library in a 384-well format. In summary, the results presented here demonstrate that this assay can be used to screen large chemical libraries to discover novel modulators of RORα.


Subject(s)
Drug Discovery/methods , High-Throughput Screening Assays , Nuclear Receptor Subfamily 1, Group F, Member 1/metabolism , Dose-Response Relationship, Drug , HEK293 Cells , Heat-Shock Proteins/metabolism , Humans , Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha , Protein Binding , Reproducibility of Results , Sensitivity and Specificity , Transcription Factors/metabolism
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