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Mass Spectrometry-Based Metabolomics: Accelerating the Characterization of Discriminating Signals by Combining Statistical Correlations and Ultrahigh Resolution

机译:基于质谱的代谢组学:通过组合统计相关性和超高分辨率来加速区分信号的表征

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摘要

A strategy combining autocorrelation matrices and ultrahigh resolution mass spectrometry (MS) was developed to optimize the characterization of discriminating ions highlighted by metabolomics. As an example, urine samples from rats treated with phenobarbital (PB) were analyzed by ultrahigh-pressure chromatography with two different eluting conditions coupled to time-of-flight mass spectrometric detection in both the positive and negative electrospray ionization modes. Multivariate data analyses were performed to highlight discriminating variables from several thousand detected signals: a few hundred signals were found to be affected by PB, whereas a few tenths of them were linked to its metabolism. Autocorrelation matrices were then applied to eliminate adduct and fragment ions. Finally, the characterization of the ions of interest was performed with ultrahigh-resolution mass spectrometry and sequential MS~(n) experiments, by using a LC-LTQ-Orbitrap system. The use of different eluting conditions was shown to drastically impact on the chromatographic retention and ionization of compounds, thus providing a way to obtain more exhaustive metabolic fingerprints, whereas autocorrelation matrices allowed one to focus the identification work on the most relevant ions. By using such an approach, 14 PB metabolites were characterized in rat urines, some of which have not been reported in the literature.
机译:开发了一种将自相关矩阵和超高分辨率质谱(MS)相结合的策略,以优化由代谢组学突出显示的区分离子的表征。例如,用超高压色谱法在正电喷雾电离和负电喷雾电离模式下结合飞行时间质谱检测,通过超高压色谱法分析了用苯巴比妥(PB)处理的大鼠的尿液样品。进行了多变量数据分析,以突出显示从数千个检测到的信号中区分出的变量:发现数百个信号受PB影响,而其中十分之一与它的代谢有关。然后应用自相关矩阵消除加合物和碎片离子。最后,使用LC-LTQ-Orbitrap系统,通过超高分辨率质谱和顺序MS〜(n)实验对目标离子进行了表征。结果表明,使用不同的洗脱条件会严重影响化合物的色谱保留和电离,从而提供了一种获取更详尽的代谢指纹的方法,而自相关矩阵使人们可以将鉴定工作集中在最相关的离子上。通过使用这种方法,在大鼠尿液中表征了14种PB代谢产物,其中一些尚未在文献中报道。

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