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MetDIA:基于数据非依赖采集的多重 MS/MS 谱图靶向代谢物提取。

MetDIA: Targeted Metabolite Extraction of Multiplexed MS/MS Spectra Generated by Data-Independent Acquisition.

机构信息

Interdisciplinary Research Center on Biology and Chemistry, and Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , Shanghai, 200032 People's Republic of China.

出版信息

Anal Chem. 2016 Sep 6;88(17):8757-64. doi: 10.1021/acs.analchem.6b02122. Epub 2016 Aug 8.

DOI:10.1021/acs.analchem.6b02122
PMID:27462997
Abstract

With recent advances in mass spectrometry, there is an increased interest in data-independent acquisition (DIA) techniques for metabolomics. With DIA technique, all metabolite ions are sequentially selected and isolated using a wide window to generate multiplexed MS/MS spectra. Therefore, DIA strategy enables a continuous and unbiased acquisition of all metabolites and increases the data dimensionality, but presents a challenge to data analysis due to the loss of the direct link between precursor ion and fragment ions. However, very few DIA data processing methods are developed for metabolomics application. Here, we developed a new DIA data analysis approach, namely, MetDIA, for targeted extraction of metabolites from multiplexed MS/MS spectra generated using DIA technique. MetDIA approach considers each metabolite in the spectral library as an analysis target. Ion chromatograms for each metabolite (both precursor ion and fragment ions) and MS(2) spectra are readily detected, extracted, and scored for metabolite identification, referred as metabolite-centric identification. A minimum metabolite-centric identification score responsible for 1% false positive rate of identification is determined as 0.8 using fully (13)C labeled biological extracts. Finally, the comparisons of our MetDIA method with data-dependent acquisition (DDA) method demonstrated that MetDIA could significantly detect more metabolites in biological samples, and is more accurate and sensitive for metabolite identifications. The MetDIA program and the metabolite spectral library is freely available on the Internet.

摘要

随着质谱技术的最新进展,人们对代谢组学中的数据非依赖性采集(DIA)技术越来越感兴趣。使用 DIA 技术,所有代谢物离子都使用宽窗口依次选择和分离,以生成多路复用的 MS/MS 光谱。因此,DIA 策略能够连续且无偏地采集所有代谢物,并增加数据的维度,但由于前体离子和碎片离子之间直接联系的丢失,对数据分析提出了挑战。然而,针对代谢组学应用,开发的 DIA 数据处理方法很少。在这里,我们开发了一种新的 DIA 数据分析方法,即 MetDIA,用于从 DIA 技术生成的多路复用 MS/MS 光谱中靶向提取代谢物。MetDIA 方法将光谱库中的每个代谢物都视为分析目标。易于检测、提取和评分每个代谢物(前体离子和碎片离子)的离子色谱图和 MS(2)光谱,用于代谢物鉴定,称为代谢物中心鉴定。使用完全(13)C 标记的生物提取物确定 0.8 的代谢物中心鉴定最低得分负责 1%的鉴定假阳性率。最后,我们的 MetDIA 方法与数据依赖采集(DDA)方法的比较表明,MetDIA 可以在生物样本中显著检测到更多的代谢物,并且在代谢物鉴定方面更准确和灵敏。MetDIA 程序和代谢物光谱库可在互联网上免费获取。

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