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蛋白质组分析系统:一种实现蛋白质组元分析与蛋白质组特征图谱绘制协调统一的工作流程。

PROTEOMAS: a workflow enabling harmonized proteomic meta-analysis and proteomic signature mapping.

作者信息

Bahl Aileen, Ibrahim Celine, Plate Kristina, Haase Andrea, Dengjel Jörn, Nymark Penny, Dumit Verónica I

机构信息

Department of Chemicals and Product Safety, German Federal Institute for Risk Assessment (BfR), Berlin, Germany.

University of Fribourg, Fribourg, Switzerland.

出版信息

J Cheminform. 2023 Mar 19;15(1):34. doi: 10.1186/s13321-023-00710-2.

Abstract

Toxicological evaluation of substances in regulation still often relies on animal experiments. Understanding the substances' mode-of-action is crucial to develop alternative test strategies. Omics methods are promising tools to achieve this goal. Until now, most attention was focused on transcriptomics, while proteomics is not yet routinely applied in toxicology despite the large number of datasets available in public repositories. Exploiting the full potential of these datasets is hampered by differences in measurement procedures and follow-up data processing. Here we present the tool PROTEOMAS, which allows meta-analysis of proteomic data from public origin. The workflow was designed for analyzing proteomic studies in a harmonized way and to ensure transparency in the analysis of proteomic data for regulatory purposes. It agrees with the Omics Reporting Framework guidelines of the OECD with the intention to integrate proteomics to other omic methods in regulatory toxicology. The overarching aim is to contribute to the development of AOPs and to understand the mode of action of substances. To demonstrate the robustness and reliability of our workflow we compared our results to those of the original studies. As a case study, we performed a meta-analysis of 25 proteomic datasets to investigate the toxicological effects of nanomaterials at the lung level. PROTEOMAS is an important contribution to the development of alternative test strategies enabling robust meta-analysis of proteomic data. This workflow commits to the FAIR principles (Findable, Accessible, Interoperable and Reusable) of computational protocols.

摘要

法规中物质的毒理学评估通常仍依赖于动物实验。了解物质的作用模式对于开发替代测试策略至关重要。组学方法是实现这一目标的有前景的工具。到目前为止,大多数关注都集中在转录组学上,而蛋白质组学尽管公共数据库中有大量数据集,但尚未在毒理学中常规应用。测量程序和后续数据处理的差异阻碍了充分利用这些数据集的潜力。在此,我们展示了PROTEOMAS工具,它允许对来自公共来源的蛋白质组数据进行荟萃分析。该工作流程旨在以统一的方式分析蛋白质组学研究,并确保出于监管目的对蛋白质组数据进行分析时的透明度。它符合经合组织的组学报告框架指南,旨在将蛋白质组学与监管毒理学中的其他组学方法整合。总体目标是为构建作用机制(AOP)做出贡献,并了解物质的作用模式。为了证明我们工作流程的稳健性和可靠性,我们将我们的结果与原始研究的结果进行了比较。作为一个案例研究,我们对25个蛋白质组学数据集进行了荟萃分析,以研究纳米材料在肺部水平的毒理学效应。PROTEOMAS对开发替代测试策略做出了重要贡献,能够对蛋白质组数据进行稳健的荟萃分析。此工作流程遵循计算协议的FAIR原则(可查找、可访问、可互操作和可重用)。

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