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A complementary approach for detecting biological signals through a semi-automated feature selection tool

dc.contributor.authorArini, Gabriel Santos
dc.contributor.authorMencucini, Luiz Gabriel Souza
dc.contributor.authorde Felício, Rafael
dc.contributor.authorFeitosa, Luís Guilherme Pereira
dc.contributor.authorRezende-Teixeira, Paula
dc.contributor.authorde Oliveira Tsuji, Henrique Marcel Yudi
dc.contributor.authorPilon, Alan Cesar [UNESP]
dc.contributor.authorPinho, Danielle Rocha
dc.contributor.authorLotufo, Letícia Veras Costa
dc.contributor.authorLopes, Norberto Peporine
dc.contributor.authorTrivella, Daniela Barretto Barbosa
dc.contributor.authorda Silva, Ricardo Roberto
dc.date.accessioned2026-04-17T14:35:10Z
dc.date.issued2024-10-25
dc.description.abstractIntroduction: Untargeted metabolomics is often used in studies that aim to trace the metabolic profile in a broad context, with the data-dependent acquisition (DDA) mode being the most commonly used method. However, this approach has the limitation that not all detected ions are fragmented in the data acquisition process, in addition to the lack of specificity regarding the process of fragmentation of biological signals. The present work aims to extend the detection of biological signals and contribute to overcoming the fragmentation limits of the DDA mode with a dynamic procedure that combines experimental and in silico approaches. Methods: Metabolomic analysis was performed on three different species of actinomycetes using liquid chromatography coupled with mass spectrometry. The data obtained were preprocessed by the MZmine software and processed by the custom package RegFilter. Results and Discussion: RegFilter allowed the coverage of the entire chromatographic run and the selection of precursor ions for fragmentation that were previously missed in DDA mode. Most of the ions selected by the tool could be annotated through three levels of annotation, presenting biologically relevant candidates. In addition, the tool offers the possibility of creating local spectral libraries curated according to the user's interests. Thus, the adoption of a dynamic analysis flow using RegFilter allowed for detection optimization and curation of potential biological signals, previously absent in the DDA mode, being a good complementary approach to the current mode of data acquisition. In addition, this workflow enables the creation and search of in-house tailored custom libraries.
dc.description.affiliationDepartment of Biomolecular Sciences, Computational Chemical Biology Laboratory, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
dc.description.affiliationNPPNS, Department of Biomolecular Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil
dc.description.affiliationDepartment of Cellular and Molecular Biology of Ribeirão Preto, Cellular and Molecular Biology Program, School of Medicine, University of São Paulo, Ribeirão Preto, Brazil
dc.description.affiliationBrazilian Biosciences National Laboratory (LNBio), Brazilian Center for Research in Energy and Materials (CNPEM), Campinas, Brazil
dc.description.affiliationDepartment of Pharmacology, Marine Pharmacology Laboratory, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil
dc.description.affiliationDepartment of Biochemistry and Organic Chemistry, Institute of Chemistry, Paulista State University, São Paulo, Brazil
dc.description.affiliationUnespDepartment of Biochemistry and Organic Chemistry, Institute of Chemistry, Paulista State University, São Paulo, Brazil
dc.identifierhttps://app.dimensions.ai/details/publication/pub.1181656190
dc.identifier.dimensionspub.1181656190
dc.identifier.doi10.3389/fchem.2024.1477492
dc.identifier.issn2296-2646
dc.identifier.orcid0000-0001-9948-2545
dc.identifier.orcid0000-0002-5773-5329
dc.identifier.orcid0000-0002-3698-940X
dc.identifier.orcid0000-0001-9855-4180
dc.identifier.orcid0000-0003-4138-8040
dc.identifier.orcid0000-0002-7244-5581
dc.identifier.orcid0000-0001-5143-2856
dc.identifier.orcid0000-0002-8159-3658
dc.identifier.orcid0000-0001-6378-0479
dc.identifier.orcid0000-0003-1861-5153
dc.identifier.pmcidPMC11543558
dc.identifier.pmid39525959
dc.identifier.urihttps://hdl.handle.net/11449/322186
dc.publisherFrontiers
dc.relation.ispartofFrontiers in Chemistry; v. 12; p. 1477492
dc.rights.accessRightsAcesso abertopt
dc.rights.sourceRightsoa_all
dc.rights.sourceRightsgold
dc.sourceDimensions
dc.titleA complementary approach for detecting biological signals through a semi-automated feature selection tool
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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