Please use this identifier to cite or link to this item: https://repositorio.inpa.gov.br/handle/1/16523
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dc.contributor.authorCavada, B. S.-
dc.contributor.authorOsterne, Vinicius José Silva-
dc.contributor.authorPinto-Junior, Vanir Reis-
dc.contributor.authorSouza, Luis Augusto Gomes-
dc.contributor.authorLóssio, Cláudia Figueiredo-
dc.contributor.authorSilva, Mayara Torquato Lima da-
dc.contributor.authorCorreia-Neto, Corneville-
dc.contributor.authorOliveira, Messias Vital-
dc.contributor.authorCorreia, Jorge Luís Almeida-
dc.contributor.authorNeco, Antonio Hadson Bastos-
dc.contributor.authorDomingos, Jorge Luiz Coelho-
dc.contributor.authorFerreira, Wandemberg Paiva-
dc.contributor.authorFarias, Gil Aquino-
dc.contributor.authorNascimento, K. S.-
dc.date.accessioned2020-06-15T21:35:09Z-
dc.date.available2020-06-15T21:35:09Z-
dc.date.issued2020-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/16523-
dc.description.abstractThe Tn antigen is an epitope containing N-acetyl-D-galactosamine present in the extracellular matrix of some carcinoma cells in humans, and it is often used as a biomarker. Lectins are proteins capable of binding to carbohydrates and can be used as a molecular tool to recognize antigens and to differentiate cancer cells from normal cells. In this context, the present work aimed to characterize the interaction of Vatairea guianensis seed lectin with N-acetyl-D-galactosamine and the Tn antigen by molecular dynamics and molecular mechanics/Poisson–Boltzmann solvent-accessible surface area analysis. This study revealed new interacting residues not previously identified in static analysis of the three-dimensional structures of Vatairea lectins, as well as the configuration taken by the carbohydrate recognition domain, as it interacts with each ligand. During the molecular dynamics simulations, Vatairea guianensis lectin was able to bind stably to Tn antigen, which, as seen previously for other lectins, enables its use in cancer research, diagnosis, and therapy. This work further demonstrates the efficiency of bioinformatics in lectinology. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 26, Número 2pt_BR
dc.rightsRestrito*
dc.subjectCarbohydrateen
dc.subjectLectinen
dc.subjectLiganden
dc.subjectN Acetylgalactosamineen
dc.subjectTn Antigenen
dc.subjectBinding Affinityen
dc.subjectCancer Researchen
dc.subjectEnergyen
dc.subjectExtracellular Matrixen
dc.subjectLegumeen
dc.subjectMolecular Dynamicsen
dc.subjectMolecular Interactionen
dc.subjectMolecular Mechanicsen
dc.subjectMolecular Recognitionen
dc.subjectNonhumanen
dc.subjectSeed Planten
dc.subjectPriority Journalen
dc.subjectSurface Areaen
dc.subjectVatairea Guianensisen
dc.titleMolecular dynamics and binding energy analysis of Vatairea guianensis lectin: a new tool for cancer studiesen
dc.typeArtigopt_BR
dc.identifier.doi10.1007/s00894-019-4281-3-
dc.publisher.journalJournal of Molecular Modelingpt_BR
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