Development of an HTS-compatible assay for discovery of RORα modulators using AlphaScreen® technology

J Biomol Screen. 2011 Feb;16(2):183-91. doi: 10.1177/1087057110389040.

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.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

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

Substances

  • Heat-Shock Proteins
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • RORA protein, human
  • Transcription Factors