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CFTR Lifecycle Map—A Systems Medicine Model of CFTR Maturation to Predict Possible Active Compound Combinations

机译:CFTR生命周期地图 - CFTR成熟的系统药模型以预测可能的活性化合物组合

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摘要

Different causative therapeutics for CF patients have been developed. There are still no mutation-specific therapeutics for some patients, especially those with rare CFTR mutations. For this purpose, high-throughput screens have been performed which result in various candidate compounds, with mostly unclear modes of action. In order to elucidate the mechanism of action for promising candidate substances and to be able to predict possible synergistic effects of substance combinations, we used a systems biology approach to create a model of the CFTR maturation pathway in cells in a standardized, human- and machine-readable format. It is composed of a core map, manually curated from small-scale experiments in human cells, and a coarse map including interactors identified in large-scale efforts. The manually curated core map includes 170 different molecular entities and 156 reactions from 221 publications. The coarse map encompasses 1384 unique proteins from four publications. The overlap between the two data sources amounts to 46 proteins. The CFTR Lifecycle Map can be used to support the identification of potential targets inside the cell and elucidate the mode of action for candidate substances. It thereby provides a backbone to structure available data as well as a tool to develop hypotheses regarding novel therapeutics.
机译:对于CF患者的不同病因治疗已经制定出来。还有没有一些患者突变特异性疗法,尤其是那些罕见的CFTR突变。为此,高通量筛选已完成的导致各种候选化合物,用行动大多不清楚模式。为了阐明其作用机制为有前途的候选物质,并能够预测物质组合的可能的协同作用,我们使用了系统生物学方法来创建CFTR成熟途径的在一个标准化的,人类和机器的细胞的模型可读格式。它是由一个芯地图,从小规模实验中的人类细胞手工辅助,和一个粗略地图包括在大规模努力鉴定相互作用物。的手工辅助芯地图包括170个不同的分子实体和从221个出版物156个反应。粗略地图涵盖了从四个出版物1384克独特的蛋白质。两个数据源之间的重叠达46克的蛋白质。该CFTR生命周期地图可以用来支持在细胞内的潜在目标的确定和阐明行动的模式候选物质。它由此提供骨干结构中可用的数据,以及制定关于新疗法的假设的工具。

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