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甲状腺激素受体与类固醇受体共调节因子2相互作用抑制剂的定量高内涵筛选

qHTS for Inhibitors of the Interaction of Thyroid Hormone Receptor and Steroid Receptor Coregulator 2

作者信息

Huang Wenwei, Johnson Ronald L, Huang Ruili, Wichterman Jennifer, Hwang Jong Yeon, Guy R Kip

机构信息

NIH Chemical Genomics Center, National Human Genome Research Institute, National Institutes of Health, Bethesda MD 20892

Department of Chemical Biology and Therapeutics, St. Jude Children’s Research Hospital, Memphis, TN38105, USA

Abstract

Thyroid hormone receptors (TRs) are members of the nuclear hormone receptor superfamily and regulate many homeostatic processes, including basal metabolism, cardiovascular function, body weight, and lipid trafficking. Upon binding of the ligand triiodothyronine (T3), TR undergoes a conformational change that releases corepressors and recruits coactivators, such as Steroid Receptor Coactivator 2 (SRC2); in turn, these modulate the expression of target genes. In this report, we used a TRβ-SRC2 fluorescence polarization assay to screen the Molecular Libraries Small Molecule Repository (MLSMR) and identify a novel methylsulfonylnitrobenzoate (MSNB)-containing series that blocks the association of TRβ with a SRC2 peptide. This inhibitor probe molecule, ML151 (CID 5184800), blocked TRβ-SRC2 interaction with a potency of 1.8μM. Mechanistic studies revealed that ML151 (CID 5184800) is a covalent inhibitor and binds irreversibly to Cys298 within the AF-2 cleft of TRβ. This series will be useful for mechanistic studies of TR-SRC2 interactions, as well as other nuclear hormone receptor-coactivator interactions.

摘要

甲状腺激素受体(TRs)是核激素受体超家族的成员,可调节许多稳态过程,包括基础代谢、心血管功能、体重和脂质转运。在配体三碘甲状腺原氨酸(T3)结合后,TR会发生构象变化,释放共抑制因子并募集共激活因子,如类固醇受体共激活因子2(SRC2);反过来,这些因子会调节靶基因的表达。在本报告中,我们使用TRβ-SRC2荧光偏振测定法筛选了分子文库小分子储存库(MLSMR),并鉴定出一个含新型甲基磺酰基硝基苯甲酸酯(MSNB)的系列化合物,该系列化合物可阻断TRβ与SRC2肽的结合。这种抑制剂探针分子ML151(化合物识别号5184800)以1.8μM的效力阻断TRβ-SRC2相互作用。机制研究表明,ML151(化合物识别号5184800)是一种共价抑制剂,可不可逆地结合到TRβ的AF-2裂隙内的半胱氨酸298上。该系列化合物将有助于TR-SRC2相互作用以及其他核激素受体-共激活因子相互作用的机制研究。

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