Most metabolomics analyses rely upon matching observed fragmentation mass spectra to library spectra for structural annotation or compare spectra with each other through network analysis. As a key part of such processes, scoring functions are used to assess the similarity between pairs of fragment spectra. No studies have so far proposed scores fundamentally different to the popular cosine-based similarity score, despite the fact that its limitations are well understood. We propose a novel spectral similarity score known as Spec2Vec which adapts algorithms from natural language processing to learn relationships between peaks from co-occurrences across large spectra datasets. We find that similarities computed with Spec2Vec i) correlate better to structural similarity than cosine-based scores, ii) subsequently gives better performance in library matching tasks, and iii) is computationally more scalable than cosine-based scores. Given the central place of similarity scoring in key metabolomics analysis tasks such as library matching and spectral networking, we expect Spec2Vec to make a broad impact in all fields that rely upon untargeted metabolomics.

The long-term integrity of neuronal axons depends on intrinsic mechanisms such as axonal transport and on extrinsic support from adjacent glial cells. This study shows that genetic defects in glia that affect axonal integrity impair the secretion of oligodendrocyte exosomes and their ability to support nutrient-deprived neurons and promote axonal transport.