| Literature DB >> 34725482 |
Roger Giné1, Jordi Capellades1,2, Josep M Badia1,2, Dennis Vughs3, Michaela Schwaiger-Haber4,5, Theodore Alexandrov6,7,8, Maria Vinaixa1,2, Andrea M Brunner3, Gary J Patti4,5, Oscar Yanes9,10.
Abstract
Comprehensive metabolome analyses are essential for biomedical, environmental, and biotechnological research. However, current MS1- and MS2-based acquisition and data analysis strategies in untargeted metabolomics result in low identification rates of metabolites. Here we present HERMES, a molecular-formula-oriented and peak-detection-free method that uses raw LC/MS1 information to optimize MS2 acquisition. Investigating environmental water, Escherichia coli, and human plasma extracts with HERMES, we achieved an increased biological specificity of MS2 scans, leading to improved mass spectral similarity scoring and identification rates when compared with a state-of-the-art data-dependent acquisition (DDA) approach. Thus, HERMES improves sensitivity, selectivity, and annotation of metabolites. HERMES is available as an R package with a user-friendly graphical interface for data analysis and visualization.Entities:
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Year: 2021 PMID: 34725482 PMCID: PMC9284938 DOI: 10.1038/s41592-021-01307-z
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 47.990