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Identification Of Compounds That Potentiate Crebsignaling As Possible Enhancers Of Long-term Memory

机译:鉴定可能使crebsignaling可能增强长期记忆的化合物

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Many studies have implicated the cAMP Response Element Binding (CREB) protein signaling pathway in long-term memory. To identify small molecule enhancers of CREB activation of gene expression, we screened ≈73,000 compounds, each at 7-15 concentrations in a quantitative high-throughput screening (qHTS) format, for activity in cells by assaying CREB mediated β-lactamase reporter gene expression. We identified 1,800 compounds that potentiated CREB mediated gene expression, with potencies as low as 16 nM, comprising 96 structural series. Mechanisms of action were systematically determined, and compounds that affect phosphodies-terase 4, protein kinase A, and cAMP production were identified, as well as compounds that affect CREB signaling via apparently unidentified mechanisms. qHTS folowed by interrogation of pathway targets is an efficient paradigm for lead generation for chemical genomics and drug development.
机译:许多研究已将cAMP反应元件结合(CREB)蛋白信号传导途径与长期记忆联系起来。为了鉴定CREB激活基因表达的小分子增强子,我们通过定量CREB介导的β-内酰胺酶报告基因表达,筛选了约73,000种化合物,每种化合物以定量高通量筛选(qHTS)格式在7-15个浓度下在细胞中具有活性。 。我们鉴定了1,800种可增强CREB介导的基因表达的化合物,其效力低至16 nM,包括96个结构序列。系统地确定了作用机理,并鉴定了影响磷酸二酯酶4,蛋白激酶A和cAMP产生的化合物,以及通过明显未知的机理影响CREB信号传导的化合物。通过询问通路目标而获得的qHTS是用于化学基因组学和药物开发的潜在客户的有效范例。

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