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使用气相色谱-化学电离飞行时间质谱法测定同位素异构体和串联质谱同位素异构体比率——方法与测量不确定度

Determination of Isotopologue and Tandem Mass Isotopologue Ratios Using Gas Chromatography Chemical Ionization Time of Flight Mass Spectrometry - Methodology and Uncertainty of Measurement.

作者信息

Mairinger Teresa, Hann Stephen

机构信息

Department of Chemistry, University of Natural Resources and Life Sciences-BOKU Vienna, Vienna, Austria.

Department of Environmental Chemistry, Eawag: Swiss Federal Institute of Aquatic Science and Technology, Duebendorf, Switzerland.

出版信息

Methods Mol Biol. 2020;2088:1-16. doi: 10.1007/978-1-0716-0159-4_1.

Abstract

The accurate and precise analysis of isotopologue and tandem mass isotopologue ratios in heavy stable isotope labeling experiments is a critical part of assessing absolute intracellular metabolic fluxes. Resulting from feeding the organism of interest with a specifically isotope-labeled substrate, the principal characteristics of these labeling experiments are the metabolites' non-naturally distributed isotopologue patterns. For the purpose of inferring metabolic rates by maximizing the fit between a priori simulated and experimentally obtained labeling patterns, C is the preferred stable isotope of use.The analysis of the obtained labeling patterns can be approached by different mass spectrometric approaches. Gas chromatography (GC) features broad metabolite coverage and excellent separation efficiency of biologically relevant isomers. These advantages compensate for laborious derivatization steps and the resulting need for interference correction for natural abundant isotopes.Here, we describe a workflow based on GC-high resolution mass spectrometry with chemical ionization for the analysis of carbon-isotopologue distributions and some positional labeling information of primary metabolites. To study the associated measurement uncertainty of the resulting C labeling patterns, guidance to uncertainty estimation according to the EURACHEM guidelines with Monte-Carlo simulation is provided.

摘要

在重稳定同位素标记实验中,对同位素异构体和串联质谱同位素异构体比率进行准确精确的分析是评估绝对细胞内代谢通量的关键部分。用特定同位素标记的底物喂养目标生物体,这些标记实验的主要特征是代谢物的非自然分布同位素异构体模式。为了通过最大化先验模拟和实验获得的标记模式之间的拟合来推断代谢率,碳是首选的稳定同位素。可以通过不同的质谱方法来分析获得的标记模式。气相色谱(GC)具有广泛的代谢物覆盖范围和对生物相关异构体出色的分离效率。这些优点弥补了繁琐的衍生化步骤以及由此产生的对天然丰度同位素进行干扰校正的需求。在此,我们描述了一种基于GC-高分辨率质谱和化学电离的工作流程,用于分析主要代谢物的碳同位素异构体分布和一些位置标记信息。为了研究所得碳标记模式的相关测量不确定度,我们根据EURACHEM指南并结合蒙特卡洛模拟提供了不确定度估计的指导。

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