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Novel Strategy for Non-Targeted Isotope-Assisted Metabolomics by Means of Metabolic Turnover and Multivariate Analysis

机译:代谢转换和多元分析的非目标同位素辅助代谢组学新策略

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摘要

Isotope-labeling is a useful technique for understanding cellular metabolism. Recent advances in metabolomics have extended the capability of isotope-assisted studies to reveal global metabolism. For instance, isotope-assisted metabolomics technology has enabled the mapping of a global metabolic network, estimation of flux at branch points of metabolic pathways, and assignment of elemental formulas to unknown metabolites. Furthermore, some data processing tools have been developed to apply these techniques to a non-targeted approach, which plays an important role in revealing unknown or unexpected metabolism. However, data collection and integration strategies for non-targeted isotope-assisted metabolomics have not been established. Therefore, a systematic approach is proposed to elucidate metabolic dynamics without targeting pathways by means of time-resolved isotope tracking, i.e., “metabolic turnover analysis”, as well as multivariate analysis. We applied this approach to study the metabolic dynamics in amino acid perturbation of Saccharomyces cerevisiae. In metabolic turnover analysis, 69 peaks including 35 unidentified peaks were investigated. Multivariate analysis of metabolic turnover successfully detected a pathway known to be inhibited by amino acid perturbation. In addition, our strategy enabled identification of unknown peaks putatively related to the perturbation.
机译:同位素标记是了解细胞代谢的有用技术。代谢组学的最新进展扩展了同位素辅助研究的能力,以揭示全球代谢。例如,同位素辅助的代谢组学技术已实现了全球代谢网络的映射,代谢途径分支点通量的估计以及将元素式分配给未知代谢物。此外,已经开发了一些数据处理工具以将这些技术应用于非目标方法,该方法在揭示未知或意外代谢方面起着重要作用。但是,尚未建立用于非目标同位素辅助代谢组学的数据收集和整合策略。因此,提出了一种系统的方法,其通过时间分辨的同位素追踪,即“代谢转换分析”以及多变量分析来阐明不以靶向途径为目标的代谢动力学。我们应用这种方法来研究酿酒酵母氨基酸扰动的代谢动力学。在代谢转换分析中,研究了69个峰,包括35个未鉴定的峰。代谢转换的多变量分析成功地检测出已知被氨基酸扰动抑制的途径。另外,我们的策略可以识别与干扰有关的未知峰。

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