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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >An integrated strategy to improve data acquisition and metabolite identification by time-staggered ion lists in UHPLC/Q-TOF MS-based metabolomics
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An integrated strategy to improve data acquisition and metabolite identification by time-staggered ion lists in UHPLC/Q-TOF MS-based metabolomics

机译:通过uHPLC / Q-TOF基于MS的代谢组学时间交错离子列表改善数据采集和代谢物鉴定的综合策略

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The narrow linear range and the limited scan time of the given ion make the quantification of the features challenging in liquid chromatography-mass spectrometry (LC–MS)-based untargeted metabolomics with the full-scan mode. And metabolite identification is another bottleneck of untargeted analysis owing to the difficulty of acquiring MS/MS information of most metabolites detected. In this study, an integrated workflow was proposed using the newly established multiple ion monitoring mode with time-staggered ion lists (tsMIM) and target-directed data-dependent acquisition with time-staggered ion lists (tsDDA) to improve data acquisition and metabolite identification in UHPLC/Q-TOF MS-based untargeted metabolomics. Compared to the conventional untargeted metabolomics, the proprosed workflow exhibited the better repeatability before and after data normalization. After selecting features with the significant change by statistical analysis, MS/MS information of all these features can be obtained by tsDDA analysis to facilitate metabolite identification. Using time-staggered ion lists, the workflow is more sensitive in data acquisition, especially for the low-abundant features. Moreover, the metabolites with low abundance tend to be wrongly integrated and triggered by full scan-based untargeted analysis with MSEacquisition mode, which can be greatly improved by the proposed workflow. The integrated workflow was also successfully applied to discover serum biosignatures for the genetic modification offat-1in mice, which indicated its practicability and great potential in future metabolomics studies.
机译:给定离子的窄线性范围和限量扫描时间使得在液相色谱 - 质谱(LC-MS)中具有挑战的特征的定量,基于全扫描模式,基于未确定的代谢组。并且代谢物鉴定是由于难以获取所检测到的大多数代谢物的MS / MS信息的难​​度而无法明确分析的另一个瓶颈。在本研究中,使用具有时间交错离子列表(TSMIM)和具有时间交错离子列表(TSDDA)的目标定向数据依赖性采集的集成工作流程,以改善数据采集和代谢物识别在UHPLC / Q-TOF基于MS的未确定代谢组科。与传统的未确定代谢组学相比,所谓的工作流程在数据标准化之前和之后表现出更好的可重复性。通过统计分析选择具有显着变化的特征后,通过TSDDA分析可以获得所有这些特征的MS / MS信息,以便于代谢物识别。使用时间交错的离子列表,工作流程在数据采集中更敏感,特别是对于低丰富的功能。此外,具有低丰度的代谢物往往是通过使用MSACQUINITION模式的全扫描的未确定分析而被错误地集成和触发,这可以通过所提出的工作流程大大提高。综合工作流程也成功地应用于发现血清生物炎,用于遗传修饰offat-1in小鼠,这表明其在未来的代谢组研究中的实用性和巨大潜力。

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