bioRxivBioinformaticsPreprint
Predicting Discrete Structural Transformations in Small Molecules from Tandem Mass Spectrometry
Xianghu WangiD, Gwendolyn KileriD, Daniela Herrera-RoseroiD, Mohammed Reza ShahnehiD, Michael J. StrobeliD, Christian GeibeliD, Yasin El AbieadiD, Vanessa V. PhelaniD, Daniel PetrasiD, Mingxun WangiD
Abstract
Tandem mass spectrometry (MS/MS) fragments molecules into smaller pieces, generating spectra composed of m/z values and intensities that encode structural information for molecular annotation. With increasing mass spectrometry data acquisition speeds, manual annotation from MS/MS lags far behind data generation and remains a bottleneck in metabolite annotation. Current computational methods, such as molecular networking, address this challenge by organizing similar structures into families of related compounds. However, they generally provide only similarity scores, offering weak actionable insights for structural annotation. To address this limitation, we present the Molecular Transformation Graph Edit Measure (MT-GEM), a distance metric that quantifies discrete structural transformations between molecules through graph edge removals that approximate structural modifications. Building on this metric, we developed an ensemble machine learning architecture, the Spectrum Transformation Edit Predictor (STEP), that builds upon TransExION and DREAMS to predict MT-GEM distances from MS/MS spectra. STEP achieves an average precision of 48.4% for identifying single structural transformations between MS/MS pairs, representing more than a tenfold improvement over state-of-the-art similarity metrics, including spectral entropy similarity (3.8%) and modified cosine (2.5%). On experimental human gut microbial community data, STEP identifies 3 times more single-transformation metabolite pairs than feature-based molecular networking at equivalent precision. In a discovery application, STEP highlights one drug metabolite and two new natural product analogs missed by modified cosine in feature-based molecular networking. By providing discrete transformation predictions rather than continuous similarity scores, MT-GEM and STEP enable hypothesis-driven metabolite annotation with testable structural modifications, which we envision will accelerate discovery of new molecules from MS/MS metabolomics datasets.
- organism: human
- assay: metabolomics
- research focus: drug response / drug discovery
- approach: machine learning (classical)
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Molecular structure discovery for untargeted metabolomics using biotransformation rules and global molecular networking
Margaret R. Martin, Wout Bittremieux, Soha Hassoun·Analytical ChemistryPeer-reviewed·Feb 4, 2025
- Learning interpretable structural similarity from tandem mass spectra for small molecule analog discovery
Juan Sebastian Piedrahita Giraldo, Katyeny Manuela da Silva, … Wout Bittremieux·bioRxiv·Jun 23, 2026
- BertMS-enabled molecular networking for unknown compounds dereplication
Luning Zhou, Wu Shuang, … Li Dehai·bioRxiv·Mar 19, 2026
- Annotating metabolite mass spectra with domain-inspired chemical formula transformers
Samuel Goldman, Jeremy Wohlwend, … Connor W. Coley·Nature Machine IntelligencePeer-reviewed·Aug 17, 2023
- Identification of metabolites from tandem mass spectra with a machine learning approach utilizing structural features
Yuanyue Li, Michael Kuhn, … Peer Bork B·BioinformaticsPeer-reviewed·Sep 26, 2019
- MESSAR: Automated recommendation of metabolite substructures from tandem mass spectra
Youzhong Liu, Aida Mrzic, … Kris Laukens·PLoS ONEPeer-reviewed·Jan 16, 2020