Erny Guillaume L, Gomes Ricardo A, Santos Mónica S F, Santos Lúcia, Neuparth Nuno, Carreiro-Martins Pedro, Marques João Gaspar, Guerreiro Ana C L, Gomes-Alves Patrícia
LEPABE - Laboratory for Process Engineering, Environment, Biotechnology and Energy, Faculdade de Engenharia da Universidade do Porto, Rua Dr. Roberto Frias, 4200-465 Porto, Portugal.
UniMS - Mass Spectrometry Unit, iBET, Av República, EAN, 2780-157 Oeiras, Portugal.
ACS Omega. 2020 Jun 23;5(26):16089-16098. doi: 10.1021/acsomega.0c01610. eCollection 2020 Jul 7.
Separation techniques hyphenated to high-resolution mass spectrometry are essential in untargeted metabolomic analyses. Due to the complexity and size of the resulting data, analysts rely on computer-assisted tools to mine for features that may represent a chromatographic signal. However, this step remains problematic, and a high number of false positives are often obtained. This work reports a novel approach where each step is carefully controlled to decrease the likelihood of errors. Datasets are first corrected for baseline drift and background noise before the MS scans are converted from profile to centroid. A new alignment strategy that includes purity control is introduced, and features are quantified using the original data with scans recorded as profile, not the extracted features. All the algorithms used in this work are part of the Finnee Matlab toolbox that is freely available. The approach was validated using metabolites in exhaled breath condensates to differentiate individuals diagnosed with asthma from patients with chronic obstructive pulmonary disease. With this new pipeline, twice as many markers were found with Finnee in comparison to XCMS-online, and nearly 50% more than with MS-Dial, two of the most popular freeware for untargeted metabolomics analysis.
与高分辨率质谱联用的分离技术在非靶向代谢组学分析中至关重要。由于所得数据的复杂性和规模,分析人员依靠计算机辅助工具来挖掘可能代表色谱信号的特征。然而,这一步骤仍然存在问题,并且经常会获得大量假阳性结果。这项工作报告了一种新颖的方法,其中每个步骤都经过仔细控制以降低出错的可能性。在将质谱扫描从轮廓图转换为质心图之前,首先对数据集进行基线漂移和背景噪声校正。引入了一种包括纯度控制的新对齐策略,并使用记录为轮廓图的原始数据而非提取的特征对特征进行定量。这项工作中使用的所有算法都是免费提供的Finnee Matlab工具箱的一部分。该方法通过呼出气冷凝物中的代谢物进行验证,以区分被诊断为哮喘的个体与慢性阻塞性肺疾病患者。使用这个新流程,与XCMS-online相比,使用Finnee发现的标志物数量增加了一倍,与MS-Dial相比增加了近50%,XCMS-online和MS-Dial是用于非靶向代谢组学分析的两种最流行的免费软件。