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Development of an HTS-Compatible Assay for Discovery of RORα Modulators Using AlphaScreen® Technology
Author(s) -
Monica A. Istrate,
Timothy Spicer,
Yan Wang,
Jerrold A. Bernard,
Leah M. Helvering,
Wayne P. Bocchinfuso,
Timothy I. Richardson,
Richard W. Zink,
Naresh Kumar,
Chahrzad MontroseRafizadeh,
Jeffrey A. Dodge,
Peter Hodder,
Patrick R. Griffin
Publication year - 2011
Publication title -
slas discovery
Language(s) - English
Resource type - Journals
eISSN - 2472-5560
pISSN - 2472-5552
DOI - 10.1177/1087057110389040
Subject(s) - drug discovery , computational biology , chemistry , biology , biochemistry
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.

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