4.7 Article

MetExpert: An expert system to enhance gas chromatography-mass spectrometry-based metabolite identifications

期刊

ANALYTICA CHIMICA ACTA
卷 1037, 期 -, 页码 316-326

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2018.03.052

关键词

Gas chromatography-Mass spectrometry; Metabolite identification; Expert system; In silico derivatization; Retention prediction; Substructure prediction

资金

  1. NSF-JST Metabolomics for a Low Carbon Society Award [1139489]
  2. University of Missouri Metabolomics Center
  3. Division Of Integrative Organismal Systems [1743594] Funding Source: National Science Foundation

向作者/读者索取更多资源

Gas chromatography. mass spectrometry (GCMS) is an important analytical technique in metabolomics studies and has been routinely used for metabolite profiling of biological samples. Spectral matching to databases of authentic compounds are the preferred tools for metabolite identifications; however, the metabolic coverage of these databases is still limited compared to the number of known metabolites. Several computational tools have been developed to facilitate the interpretation of MS data but unfortunately most of them have limited applicability to GCMS-based metabolite identification. In this paper, we introduce a computer-aided, metabolite expert system called MetExpert which emulates the metabolite-identification ability of a human expert using orthogonal datasets including molecular formulas, retention indices, and EI-MS spectra to characterize the molecular structures. This system integrates four modules including in silico derivatization, metabolite-likeness evaluation, retention prediction, and substructure prediction. In silico derivatization increases the searchable chemical space for TMS-derivatized metabolites many of which are absent in molecular structure databases. Metabolite-likeness evaluations are an efficient approach to select metabolite-like molecules when querying large databases such as PubChem. An artificial neutral network then establishes the quantitative structure. retention relationships for the accurate prediction of RIs that further refines the candidate molecules. In addition, PLS-DA models establish quantitative structure. spectra relationships for the prediction of metabolite substructures. Finally, weighted scoring of three orthogonal evaluations increases the identification rates. MetExpert outperformed current state-of-the-art methods such as MetFrag and CFM-ID for ranking the correct identifications. While spectral comparisons with chemical standards or de novo structural elucidations are necessary to validate the predictions, MetExpert provides an efficient and effective approach to prioritize the candidates. (C) 2018 Elsevier B.V. All rights reserved.

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