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Comparison of GC-MS and GC×GC-MS in the Analysis of Human Serum Samples for Biomarker Discovery

机译:GC-MS和GC×GC-MS在用于生物标志物发现的人血清样品分析中的比较

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摘要

We compared the performance of gas chromatography time-of-flight mass spectrometry (GC-MS) and comprehensive two-dimensional gas chromatography mass spectrometry (GC×GC-MS) for metabolite biomarker discovery. Metabolite extracts from 109 human serum samples were analyzed on both platforms with a pooled serum sample analyzed after every 9 biological samples for the purpose of quality control (QC). The experimental data derived from the pooled QC samples showed that the GC×GC-MS platform detected about three times as many peaks as the GC-MS platform at a signal-to-noise ratio SNR ≥ 50, and three times the number of metabolites were identified by mass spectrum matching with a spectral similarity score Rsim ≥ 600. Twenty-three metabolites had statistically significant abundance changes between the patient samples and the control samples in the GC-MS data set while 34 metabolites in the GC×GC-MS data set showed statistically significant differences. Among these two groups of metabolite biomarkers, nine metabolites were detected in both the GC-MS and GC×GC-MS data sets with the same direction and similar magnitude of abundance changes between the control and patient sample groups. Manual verification indicated that the difference in the number of the biomarkers discovered using these two platforms was mainly due to the limited resolution of chromatographic peaks by the GC-MS platform, which can result in severe peak overlap making subsequent spectrum deconvolution for metabolite identification and quantification difficult.
机译:我们比较了气相色谱飞行时间质谱(GC-MS)和全面二维气相色谱质谱(GC×GC-MS)在代谢物生物标记物发现方面的性能。在两个平台上分析了来自109个人血清样品的代谢物提取物,每9个生物样品后分析了合并的血清样品,以进行质量控制(QC)。从合并的QC样品获得的实验数据表明,在信噪比SNR≥50时,GC×GC-MS平台检测到的峰大约是GC-MS平台的三倍,而代谢物数量的三倍质谱相似性得分Rsim≥600进行质谱匹配鉴定。GC-MS数据集中有23种代谢物在患者样品和对照样品之间具有统计学上的显着变化,而GC×GC-MS数据中有34种代谢物集显示出统计学上的显着差异。在这两组代谢物生物标志物中,在GC-MS和GC×GC-MS数据集中检测到9种代谢物,对照组和患者样品组的方向相同,丰度变化幅度相似。手动验证表明,使用这两个平台发现的生物标志物数量的差异主要是由于GC-MS平台对色谱峰的分辨率有限,这可能导致严重的峰重叠,从而导致随后的光谱去卷积用于代谢物鉴定和定量难。

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