Adaptive Modeling of Tandem Mass Spectrometry Data: Creation of the METLIN 960K MRM Database

Multiple Reaction Monitoring (MRM) remains the gold standard for quantitative mass spectrometry but continues to be constrained by the limited availability of high-quality transitions and collision energy (CE) values for many biologically and chemically relevant molecules. Here, we present the METLIN 960K MRM library, a 960,000-compound transition resource derived entirely from empirically acquired MS/MS data. MRM transitions were generated in both positive and negative ionization modes using an empirical spline-based pipeline refined by AI BioSync, an XCMS enhancement that provides a framework of AI and machine-learning tools designed to decipher spectral data for biological and analytical relevance. Central to this approach is spline fitting of CE-dependent intensity profiles from experimental MS/MS data collected at four discrete energies (0, 10, 20, and 40 eV), enabling continuous CE modeling and precise prediction of optimal fragmentation conditions. Supervised learning models were used within AI BioSync to refine spline fitting across diverse chemical classes, improving reproducibility and predictive accuracy. Validation across more than 100 authentic compounds, including rare metabolites and diverse small molecules, demonstrated robust detection down to 1 nM, confirming both sensitivity and scalability. This framework also holds immediate applicability for preclinical drug development studies, where authentic metabolite and impurity standards are often unavailable. Unlike prior methods reliant on <i>in silico</i> fragmentation or heuristic rules, all transitions are derived directly from experimental MS/MS data using absolute intensities. The resulting precursor <i>m</i>/<i>z</i>-centric METLIN 960K MRM library (https://metlin.scripps.edu) greatly expands the chemical space accessible to targeted quantitation, providing a scalable, vendor-independent path for sensitive and specific molecular detection across research, clinical, and applied applications.

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Publication Details

Journal
Analytical Chemistry
Published
2025-10-28
DOI
https://doi.org/10.1021/acs.analchem.5c04639
Citations
2
Primary Topic
Mass Spectrometry Techniques and Applications
Type
article
Field-Weighted Citation Impact
1.51
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article

Adaptive Modeling of Tandem Mass Spectrometry Data: Creation of the METLIN 960K MRM Database

Robert S. Plumb, Aries Aisporna, Winnie Uritboonthai, Bill Webb et al.
2 citations
Analytical Chemistry
Mass Spectrometry Techniques and Applications
1.51
article

Adaptive Modeling of Tandem Mass Spectrometry Data: Creation of the METLIN 960K MRM Database

Robert S. Plumb, Aries Aisporna, Winnie Uritboonthai, Bill Webb, Gary Siuzdak, Elizabeth Billings, Corey Hoang, Linh Hoang
article en
2 citations

Abstract

Multiple Reaction Monitoring (MRM) remains the gold standard for quantitative mass spectrometry but continues to be constrained by the limited availability of high-quality transitions and collision energy (CE) values for many biologically and chemically relevant molecules. Here, we present the METLIN 960K MRM library, a 960,000-compound transition resource derived entirely from empirically acquired MS/MS data. MRM transitions were generated in both positive and negative ionization modes using an empirical spline-based pipeline refined by AI BioSync, an XCMS enhancement that provides a framework of AI and machine-learning tools designed to decipher spectral data for biological and analytical relevance. Central to this approach is spline fitting of CE-dependent intensity profiles from experimental MS/MS data collected at four discrete energies (0, 10, 20, and 40 eV), enabling continuous CE modeling and precise prediction of optimal fragmentation conditions. Supervised learning models were used within AI BioSync to refine spline fitting across diverse chemical classes, improving reproducibility and predictive accuracy. Validation across more than 100 authentic compounds, including rare metabolites and diverse small molecules, demonstrated robust detection down to 1 nM, confirming both sensitivity and scalability. This framework also holds immediate applicability for preclinical drug development studies, where authentic metabolite and impurity standards are often unavailable. Unlike prior methods reliant on <i>in silico</i> fragmentation or heuristic rules, all transitions are derived directly from experimental MS/MS data using absolute intensities. The resulting precursor <i>m</i>/<i>z</i>-centric METLIN 960K MRM library (https://metlin.scripps.edu) greatly expands the chemical space accessible to targeted quantitation, providing a scalable, vendor-independent path for sensitive and specific molecular detection across research, clinical, and applied applications.

Analytical ChemistryVol. 97(44)
Scripps Research Institute (US), University of Liverpool (GB), Netherlands Metabolomics Centre (NL), Structural Integrity Associates (United States) (US)
Openalex Percentile: Top 15%
Mass Spectrometry Techniques and Applications
1.51
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