Untargeted metabolomics approaches deal with complex data hindering structural information for the comprehensive analysis of unknown metabolite features. We investigated the metabolite discovery capacity and the possible extension of the annotation coverage of the Feature-Based Molecular Networking (FBMN) approach by adding two novel nutritionally-relevant (contextual) mass spectral libraries to the existing public ones, as compared to widely-used open-source annotation protocols. Two contextual mass spectral libraries in positive and negative ionization mode of ~300 reference molecules relevant for plant-based nutrikinetic studies were created and made publicly available through the GNPS platform. The postprandial urinary metabolome analysis within the intervention of Vaccinium supplements was selected as a case study. Following the FBMN approach in combination with the added contextual mass spectral libraries, 67 berry-related and human endogenous metabolites were annotated, achieving a structural annotation coverage comparable to or higher than existing non-commercial annotation workflows. To further exploit the quantitative data obtained within the FBMN environment, the postprandial behavior of the annotated metabolites was analyzed with Pearson product-moment correlation. This simple chemometric tool linked several molecular families with phase II and phase I metabolism. The proposed approach is a powerful strategy to employ in longitudinal studies since it reduces the unknown chemical space by boosting the annotation power to characterize biochemically relevant metabolites in human biofluids

Renai, L.; Ulaszewska, M.; Mattivi, F.; Bartoletti, R.; Del Bubba, M.; van der Hooft, J.J.J. (2022-10-21). Combining feature-based molecular networking and contextual mass spectral libraries to decipher nutrimetabolomics profiles. METABOLITES, 12 (10): 1005. doi: 10.3390/metabo12101005 handle: https://hdl.handle.net/10449/85316

Combining feature-based molecular networking and contextual mass spectral libraries to decipher nutrimetabolomics profiles

Ulaszewska, M.
;
Mattivi, Fulvio;
2022-10-21

Abstract

Untargeted metabolomics approaches deal with complex data hindering structural information for the comprehensive analysis of unknown metabolite features. We investigated the metabolite discovery capacity and the possible extension of the annotation coverage of the Feature-Based Molecular Networking (FBMN) approach by adding two novel nutritionally-relevant (contextual) mass spectral libraries to the existing public ones, as compared to widely-used open-source annotation protocols. Two contextual mass spectral libraries in positive and negative ionization mode of ~300 reference molecules relevant for plant-based nutrikinetic studies were created and made publicly available through the GNPS platform. The postprandial urinary metabolome analysis within the intervention of Vaccinium supplements was selected as a case study. Following the FBMN approach in combination with the added contextual mass spectral libraries, 67 berry-related and human endogenous metabolites were annotated, achieving a structural annotation coverage comparable to or higher than existing non-commercial annotation workflows. To further exploit the quantitative data obtained within the FBMN environment, the postprandial behavior of the annotated metabolites was analyzed with Pearson product-moment correlation. This simple chemometric tool linked several molecular families with phase II and phase I metabolism. The proposed approach is a powerful strategy to employ in longitudinal studies since it reduces the unknown chemical space by boosting the annotation power to characterize biochemically relevant metabolites in human biofluids
Bioinformatics
Chemometrics
Computational metabolomics
Human urine
Liquid chromatography
Untargeted mass spectrometry
Settore CHIM/10 - CHIMICA DEGLI ALIMENTI
21-ott-2022
Renai, L.; Ulaszewska, M.; Mattivi, F.; Bartoletti, R.; Del Bubba, M.; van der Hooft, J.J.J. (2022-10-21). Combining feature-based molecular networking and contextual mass spectral libraries to decipher nutrimetabolomics profiles. METABOLITES, 12 (10): 1005. doi: 10.3390/metabo12101005 handle: https://hdl.handle.net/10449/85316
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