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Abstract
<jats:p>Molecular imaging by imaging mass spectrometry (IMS) has become a key modality for spatial proteomics, lipidomics, glycomics, and metabolomics. It maps hundreds to thousands of molecular species con-currently throughout tissue without prior labeling. However, reporting thousands of ion images makes IMS measurements very high-dimensional, complicating interpretation. Furthermore, IMS data contain implicit chemical relationships. For example, the same molecular species can be re-ported by several separately-measured ion species, each an isotopic variant or isotopologue of that molecule. While conventional dimensionality reduction methods such as principal component analysis can address the dimensionality challenge, they typically do not preserve chemical relationships (e.g., isotopologue grouping), making biological interpretation harder. As advanced, higher-dimensional measurement types such as ion mobility IMS (IM-IMS) expand into spatial omics, addressing interpretability in a chemically informed way becomes pressing. Therefore, we present IsoMobil, a dimensionality-reduction framework for IM-IMS data that empirically detects potential isotopologues. Besides reducing dataset complexity, it facilitates interpretation at the (biologically relevant) molecular-species level rather than ion-species level. The algorithm finds spatially coherent ion species, filters them based on isotope-induced mass-to-charge (m/z ) distances and mobility-bin consistency (isotopo-logues have near-identical collisional cross-sections). This yields a compact representation where isotopologue-candidate families, rather than individual ion-species, form latent dimensions. In a synthetic benchmark, IsoMobil outperformed (F1=1.0) spatial-only and m/z -based methods (F1≈0.67). In a human colon case study, IsoMobil found 77 isotopologue-candidate groups (COSH-P-quality≥0.85) among 6344 lipid ion species. By automating isotopologue discovery, IsoMobil lifts biological interpretation of exploratory, untargeted spatial omics by IM-IMS to the molecular-species level.</jats:p>