An Untargeted Metabolomic Workflow to Improve Structural Characterization of Metabolites

• Published in: Analytical chemistry (Washington) Vol. 85; no. 16; pp. 7713 - 7719
• Main Authors: Nikolskiy, Igor, Mahieu, Nathaniel G, Chen, Ying-Jr, Tautenhahn, Ralf, Patti, Gary J
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 20-08-2013
• Subjects: Algorithms; Cell Line, Transformed; Chromatography, Liquid; Contamination; Fragments; Humans; Mass Spectrometry; Metabolites; Metabolomics; Molecular Conformation; Performance evaluation; Simulation; Spectra; Spectrum analysis; Structural analysis; Windows (computer programs); Workflow
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac400751j

Mass spectrometry-based metabolomics relies on MS2 data for structural characterization of metabolites. To obtain the high-quality MS2 data necessary to support metabolite identifications, ions of interest must be purely isolated for fragmentation. Here, we show that metabolomic MS2 data are frequently characterized by contaminating ions that prevent structural identification. Although using narrow-isolation windows can minimize contaminating MS2 fragments, even narrow windows are not always selective enough, and they can complicate data analysis by removing isotopic patterns from MS2 spectra. Moreover, narrow windows can significantly reduce sensitivity. In this work, we introduce a novel, two-part approach for performing metabolomic identifications that addresses these issues. First, we collect MS2 scans with less stringent isolation settings to obtain improved sensitivity at the expense of specificity. Then, by evaluating MS2 fragment intensities as a function of retention time and precursor mass targeted for MS2 analysis, we obtain deconvolved MS2 spectra that are consistent with pure standards and can therefore be used for metabolite identification. The value of our approach is highlighted with metabolic extracts from brain, liver, astrocytes, as well as nerve tissue, and performance is evaluated by using pure metabolite standards in combination with simulations based on raw MS2 data from the METLIN metabolite database. A R package implementing the algorithms used in our workflow is available on our laboratory website (http://pattilab.wustl.edu/decoms2.php).