Drug and drug target identification for Friedreich ataxia

Friedreich 共济失调的药物和药物靶点鉴定

• 批准号: 7143801
• 负责人: ROBERT B WILSON
• 金额: $ 17.66万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-01 至 2008-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7143801
• 关键词: ataxia; fibroblasts; genetics; library; model; proteins; yeasts

DESCRIPTION (provided by applicant): We developed a primary, high-throughput drug-screening assay for Friedreich ataxia (FRDA) using a yeast model system, as well as a secondary screening assay using primary FRDA fibroblasts. Both assays are phenotypic and are based on the critical role of mitochondrial dysfunction in the signs and symptoms of FRDA. In the primary assay we turn off the expression of the yeast frataxin homologue, Yfh1p, using an inducible/repressible promoter, and then follow mitochondrial function in 96-well plates using a simple spectrophotometric readout. We optimized our assay to S/B values of > 8, and Z' scores of > 0.7. We successfully implemented our assay at the Southern Research Institute, which is in the process of screening the 102,000-compound NINDS library. The Southern Research Institute will also perform counter-screens (to identify false-positives) and dose-response analyses of all bona fide hit compounds. This proposal describes our plan to: 1) prioritize hit compounds based on secondary assays in yeast and human cells, 2) determine mechanisms of action, and 3) identify potential target proteins and pathways for FRDA therapeutics. Our overall goal is to identify compounds and cellular targets for the treatment of FRDA. Our Specific Aims are: 1. To test hit compounds from the primary screen in a secondary yeast assay. We will determine the effects of hit compounds on overall ATP production in the yeast model of FRDA. 2. To test compounds from Aim 1 in primary FRDA fibroblasts. We will determine the effects of compounds on tetrazolium dye reduction and on survival in the context of glutathione depletion. 3. To test compounds for mechanisms of action. We will take advantage of the complete library of yeast knockout strains to determine target proteins and pathways. We will confirm our findings in primary FRDA fibroblasts. 4. To perform a genetic suppressor analysis of Yfh1 -depleted cells. We will take advantage of the complete library of yeast knockout strains to identify additional target proteins and pathways using genetic suppressor analysis. We will confirm our findings in primary FRDA fibroblasts.

描述（由申请人提供）：我们使用酵母模型系统开发了用于Friedreich共济失调（FRDA）的主要高通量药物筛查测定法，以及使用主要FRDA成纤维细胞的次级筛选测定法。两种测定都是表型，并且基于线粒体功能障碍在FRDA的体征和症状中的关键作用。在主要测定中，我们使用可诱导/抑制启动子关闭酵母frataxin同源物YFH1P的表达，然后使用简单的分光光度计读数在96孔板中遵循96孔板的线粒体功能。我们将测定优化为> 8的S/B值，Z'分数> 0.7。我们在南方研究所成功实施了我们的测定法，该研究所正在筛选102,000个杂交的Ninds图书馆。南方研究所还将进行反屏幕（以识别假阳性）和所有真正的命中化合物的剂量反应分析。该提案描述了我们的计划：1）基于酵母和人类细胞中的二级测定的命中化合物的优先级，2）确定作用机理，3）确定frda疗法的潜在靶蛋白和途径。我们的总体目标是确定FRDA治疗的化合物和细胞靶标。我们的具体目的是：1。在次级酵母测定中测试主屏幕上的命中化合物。我们将确定HIT化合物对FRDA酵母模型中总ATP产生的影响。 2。在主要FRDA成纤维细胞中的AIM 1测试化合物。我们将确定化合物对谷胱甘肽耗竭背景下四唑次染料还原和生存的影响。 3。测试化合物的作用机理。我们将利用完整的酵母敲除菌株库来确定靶蛋白和途径。我们将在主要FRDA成纤维细胞中确认我们的发现。 4。进行YFH1缺失细胞的遗传抑制分析。我们将利用酵母敲除菌株的完整库，使用遗传抑制剂分析来识别其他靶蛋白和途径。我们将在主要FRDA成纤维细胞中确认我们的发现。