首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Integrating comprehensive two-dimensional gas chromatography mass spectrometry and parallel two-dimensional liquid chromatography mass spectrometry for untargeted metabolomics
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Integrating comprehensive two-dimensional gas chromatography mass spectrometry and parallel two-dimensional liquid chromatography mass spectrometry for untargeted metabolomics

机译:整合综合二维气相色谱质谱与并联二维液相色谱法质谱,以实现未明确的代谢组学

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The diverse characteristics and large number of entities make metabolite separation challenging in metabolomics. To date, there is not a singular instrument capable of analyzing all types of metabolites. In order to achieve a better separation for higher peak capacity and accurate metabolite identification and quantification, we integrated GC x GC-MS and parallel 2DLC-MS for analysis of polar metabolites. To test the performance of the developed system, 13 rats were fed different diets to form two animal groups. Polar metabolites extracted from rat livers were analyzed by GC x GC-MS, parallel 2DLC-MS (-) and parallel 2DLC-MS (+), respectively. By integrating all data together, 58 metabolites were detected with significant change in their abundance levels between groups (p <= 0.05). Of the 58 metabolites, three metabolites were detected in two platforms and two in all three platforms. Manual examination showed that discrepancy of metabolite regulation measured by different platforms was mainly caused by the poor shape of chromatographic peaks resulting from low instrument response. Pathway analysis demonstrated that integrating the results from multiple platforms increased the confidence of metabolic pathway assignment.
机译:不同的特点和大量实体使代谢物分离在代谢组织中具有挑战性。迄今为止,没有能够分析所有类型代谢物的奇异仪器。为了实现更高的峰值容量和准确的代谢物鉴定和定量的更好分离,我们集成了GC X GC-MS和并联2DLC-MS以分析极性代谢物。为了测试发达系统的性能,将13只大鼠喂食不同的饮食以形成两种动物组。通过GC X GC-MS,并联2DLC-MS(+)分析从大鼠肝脏中提取的极性代谢物。通过将所有数据集成在一起,检测到58个代谢物,在组之间的丰度水平的显着变化(P <= 0.05)。在58个代谢物中,在两个平台中检测到三种代谢物,在所有三个平台中都有两个。手动检查表明,不同平台测量的代谢物调节的差异主要是由于低仪器响应产生的色谱峰的差。途径分析表明,集成多个平台的结果增加了代谢途径分配的置信度。

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