Literature DB >> 21482722

A quantitative high-throughput screen identifies novel inhibitors of the interaction of thyroid receptor beta with a peptide of steroid receptor coactivator 2.

Ronald L Johnson1, Jong Yeon Hwang, Leggy A Arnold, Ruili Huang, Jennifer Wichterman, Indre Augustinaite, Christopher P Austin, James Inglese, R Kiplin Guy, Wenwei Huang.   

Abstract

The thyroid hormone receptors (TR) are members of the nuclear hormone receptor (NHR) superfamily that regulate development, growth, and metabolism. Upon ligand binding, TR releases bound corepressors and recruits coactivators to modulate target gene expression. Steroid receptor coactivator 2 (SRC2) is an important coregulator that interacts with TRβ to activate gene transcription. To identify novel inhibitors of the TRβ and SRC2 interaction, the authors performed a quantitative high-throughput screen (qHTS) of a TRβ-SRC2 fluorescence polarization assay against more than 290 000 small molecules. The qHTS assayed compounds at 6 concentrations up to 92 µM to generate titration-response curves and determine the potency and efficacy of all compounds. The qHTS data set enabled the characterization of actives for structure-activity relationships as well as for potential artifacts such as fluorescence interference. Selected qHTS actives were tested in the screening assay using fluoroprobes labeled with Texas Red or fluorescein. The retest identified 19 series and 4 singletons as active in both assays with 40% or greater efficacy, free of compound interference, and not toxic to mammalian cells. Selected compounds were tested as independent samples, and a methylsulfonylnitrobenzoate series inhibited the TRβ-SRC2 interaction with 5 µM IC(50). This series represents a new class of thyroid hormone receptor-coactivator modulators.

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Year:  2011        PMID: 21482722      PMCID: PMC3162318          DOI: 10.1177/1087057111402199

Source DB:  PubMed          Journal:  J Biomol Screen        ISSN: 1087-0571


  33 in total

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Authors:  J C Owicki
Journal:  J Biomol Screen       Date:  2000-10

2.  Real experiences of uHTS: a prototypic 1536-well fluorescence anisotropy-based uHTS screen and application of well-level quality control procedures.

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Journal:  J Biomol Screen       Date:  2001-10

Review 3.  Physiological and molecular basis of thyroid hormone action.

Authors:  P M Yen
Journal:  Physiol Rev       Date:  2001-07       Impact factor: 37.312

Review 4.  Nuclear hormone receptors and gene expression.

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Journal:  Physiol Rev       Date:  2001-07       Impact factor: 37.312

5.  Steroid receptor coactivator peptidomimetics.

Authors:  Timothy R Geistlinger; R Kiplin Guy
Journal:  Methods Enzymol       Date:  2003       Impact factor: 1.600

6.  Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor.

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Review 7.  The SRC family of nuclear receptor coactivators.

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Journal:  Gene       Date:  2000-03-07       Impact factor: 3.688

8.  Methylsulfonylnitrobenzoates, a new class of irreversible inhibitors of the interaction of the thyroid hormone receptor and its obligate coactivators that functionally antagonizes thyroid hormone.

Authors:  Jong Yeon Hwang; Wenwei Huang; Leggy A Arnold; Ruili Huang; Ramy R Attia; Michele Connelly; Jennifer Wichterman; Fangyi Zhu; Indre Augustinaite; Christopher P Austin; James Inglese; Ronald L Johnson; R Kiplin Guy
Journal:  J Biol Chem       Date:  2011-02-14       Impact factor: 5.157

9.  Geneserine and geneseroline revisited: acid-base catalyzed equilibria of hexahydropyrrolo-[2,3-b]-indole N-oxides with hexahydro-1,2-oxazino-[5,6-b]-indoles.

Authors:  Q S Yu; H J Yeh; A Brossi; J L Flippen-Anderson
Journal:  J Nat Prod       Date:  1989 Mar-Apr       Impact factor: 4.050

Review 10.  Review of the in vivo functions of the p160 steroid receptor coactivator family.

Authors:  Jianming Xu; Qingtian Li
Journal:  Mol Endocrinol       Date:  2003-06-12
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  5 in total

Review 1.  Thyroid disrupting chemicals and developmental neurotoxicity - New tools and approaches to evaluate hormone action.

Authors:  Katherine L O'Shaughnessy; Mary E Gilbert
Journal:  Mol Cell Endocrinol       Date:  2019-11-21       Impact factor: 4.102

2.  Methylsulfonylnitrobenzoates, a new class of irreversible inhibitors of the interaction of the thyroid hormone receptor and its obligate coactivators that functionally antagonizes thyroid hormone.

Authors:  Jong Yeon Hwang; Wenwei Huang; Leggy A Arnold; Ruili Huang; Ramy R Attia; Michele Connelly; Jennifer Wichterman; Fangyi Zhu; Indre Augustinaite; Christopher P Austin; James Inglese; Ronald L Johnson; R Kiplin Guy
Journal:  J Biol Chem       Date:  2011-02-14       Impact factor: 5.157

3.  Synthesis and evaluation of sulfonylnitrophenylthiazoles (SNPTs) as thyroid hormone receptor-coactivator interaction inhibitors.

Authors:  Jong Yeon Hwang; Ramy R Attia; Fangyi Zhu; Lei Yang; Andrew Lemoff; Cynthia Jeffries; Michele C Connelly; R Kiplin Guy
Journal:  J Med Chem       Date:  2012-02-23       Impact factor: 7.446

4.  Deficiency of thyroid hormone receptor protects retinal pigment epithelium and photoreceptors from cell death in a mouse model of age-related macular degeneration.

Authors:  Hongwei Ma; Fan Yang; Xi-Qin Ding
Journal:  Cell Death Dis       Date:  2022-03-21       Impact factor: 8.469

Review 5.  Chemical Screening of Nuclear Receptor Modulators.

Authors:  Mari Ishigami-Yuasa; Hiroyuki Kagechika
Journal:  Int J Mol Sci       Date:  2020-07-31       Impact factor: 5.923

  5 in total

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