Molecular Design Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.
J Med Chem. 2012 Jun 14;55(11):4978-89. doi: 10.1021/jm300068n. Epub 2012 May 24.
We describe a fully customizable and integrated target-specific "tiered" virtual screening approach tailored to identifying and characterizing novel peroxisome proliferator activated receptor γ (PPARγ) scaffolds. Built on structure- and ligand-based computational techniques, a consensus protocol was developed for use in the virtual screening of chemical databases, focused toward retrieval of novel bioactive chemical scaffolds for PPARγ. Consequent from application, three novel PPAR scaffolds displaying distinct chemotypes have been identified, namely, 5-(4-(benzyloxy)-3-chlorobenzylidene)dihydro-2-thioxopyrimidine-4,6(1H,5H)-dione (MDG 548), 3-((4-bromophenoxy)methyl)-N-(4-nitro-1H-pyrazol-1-yl)benzamide (MDG 559), and ethyl 2-[3-hydroxy-5-(5-methyl-2-furyl)-2-oxo-4-(2-thienylcarbonyl)-2,5-dihydro-1H-pyrrol-1-yl]-4-methyl-1,3-thiazole-5-carboxylate (MDG 582). Fluorescence polarization(FP) and time resolved fluorescence resonance energy transfer (TR-FRET) show that these compounds display high affinity competitive binding to the PPARγ-LBD (EC(50) of 215 nM to 5.45 μM). Consequent characterization by a TR-FRET activation reporter assay demonstrated agonism of PPARγ by all three compounds (EC(50) of 467-594 nM). Additionally, differential PPAR isotype specificity was demonstrated through assay against PPARα and PPARδ subtypes. This work showcases the ability of target specific "tiered screen" protocols to successfully identify novel scaffolds of individual receptor subtypes with greater efficacy than isolated screening methods.
我们描述了一种完全可定制和集成的针对特定靶标的“分层”虚拟筛选方法,旨在识别和表征新型过氧化物酶体增殖物激活受体γ(PPARγ)支架。该方法建立在结构和配体基于计算技术的基础上,开发了一种共识协议,用于化学数据库的虚拟筛选,旨在检索新型生物活性化学支架用于 PPARγ。应用后,已经确定了三种新型的 PPAR 支架,它们具有不同的化学类型,分别为 5-(4-(苄氧基)-3-氯亚苄基)二氢-2-硫代嘧啶-4,6(1H,5H)-二酮(MDG 548)、3-((4-溴苯氧基)甲基)-N-(4-硝基-1H-吡唑-1-基)苯甲酰胺(MDG 559)和乙基 2-[3-羟基-5-(5-甲基-2-呋喃基)-2-氧代-4-(2-噻吩羰基)-2,5-二氢-1H-吡咯-1-基]-4-甲基-1,3-噻唑-5-羧酸酯(MDG 582)。荧光偏振(FP)和时间分辨荧光共振能量转移(TR-FRET)表明,这些化合物对 PPARγ-LBD 具有高亲和力的竞争性结合(EC50 为 215 nM 至 5.45 μM)。随后通过 TR-FRET 激活报告基因测定对其进行了特征分析,证明了这三种化合物均对 PPARγ 具有激动作用(EC50 为 467-594 nM)。此外,通过针对 PPARα 和 PPARδ 亚型的测定证明了不同的 PPAR 同工型特异性。这项工作展示了针对特定靶标的“分层筛选”协议成功识别新型单个受体亚型支架的能力,其功效优于单独的筛选方法。