Mañana, JUEVES, 24 DE ABRIL, el sistema se apagará debido a tareas habituales de mantenimiento a partir de las 9 de la mañana. Lamentamos las molestias.

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dc.contributor.authorRuiz-Márvez, Elizabeth
dc.contributor.authorRamírez, César Augusto
dc.contributor.authorRodríguez, Eliana Rocío
dc.contributor.authorFlórez, Magda Mellisa
dc.contributor.authorDelgado, Gabriela
dc.contributor.authorGuzmán, Fanny
dc.contributor.authorGómez-Puertas, Paulino
dc.contributor.authorRequena Rolania, José María 
dc.contributor.authorPuerta, Concepción J.
dc.contributor.otherUAM. Departamento de Biología Moleculares_ES
dc.date.accessioned2021-04-08T08:52:55Z
dc.date.available2021-04-08T08:52:55Z
dc.date.issued2020-03-31
dc.identifier.citationInternational Journal of Molecular Sciences 21.7 (2020): 2432en_US
dc.identifier.issn1422-0067es_ES
dc.identifier.urihttp://hdl.handle.net/10486/694459
dc.description.abstractThe Tc964 protein was initially identified by its presence in the interactome associated with the LYT1 mRNAs, which code for a virulence factor of Trypanosoma cruzi. Tc964 is annotated in the T. cruzi genome as a hypothetical protein. According to phylogenetic analysis, the protein is conserved in the different genera of the Trypanosomatidae family; however, recognizable orthologues were not identified in other groups of organisms. Therefore, as a first step, an in-depth molecular characterization of the Tc946 protein was carried out. Based on structural predictions and molecular dynamics studies, the Tc964 protein would belong to a particular class of GTPases. Subcellular fractionation analysis indicated that Tc964 is a nucleocytoplasmic protein. Additionally, the protein was expressed as a recombinant protein in order to analyze its antigenicity with sera from Chagas disease (CD) patients. Tc964 was found to be antigenic, and B-cell epitopes were mapped by the use of synthetic peptides. In parallel, the Leishmania major homologue (Lm964) was also expressed as recombinant protein and used for a preliminary evaluation of antigen cross-reactivity in CD patients. Interestingly, Tc964 was recognized by sera from Chronic CD (CCD) patients at different stages of disease severity, but no reactivity against this protein was observed when sera from Colombian patients with cutaneous leishmaniasis were analyzed. Therefore, Tc964 would be adequate for CD diagnosis in areas where both infections (CD and leishmaniasis) coexist, even though additional assays using larger collections of sera are needed in order to confirm its usefulness for differential serodiagnosisen_US
dc.description.sponsorshipThis research was funded by Ministerio de Ciencia,Tecnología e Innovación (Minciencias) and Pontificia Universidad Javeriana, research project ID PPTA 120356933228 granted to C.J.P. The article publication was funded by the Vicerrectoría de Investigación from the Pontificia Universidad Javeriana, code 120813F0401200. The Network of Tropical Diseases Research RICET (RD16/0027/0008, Instituto de Salud Carlos III and co-funded by FEDER) to J.M.R., and grants from the Spanish Ministerio de Ciencia, Innovación y Universidades/Agencia Estatal de Investigación RTC-2017-6494-1 and RTI2018-094434-B-I00 (MCIU/AEI/FEDER, UE) to P.G.-P., E.R.-M and E.R.R. were supported by Minciencias convocatoria doctorados nacionales 647-2014 and convocatoria jóvenes investigadores e innovadores 706-2015, respectivelyen_US
dc.format.extent19 pag.es_ES
dc.format.mimetypeapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relation.ispartofInternational Journal of Molecular Sciencesen_US
dc.rights© 2020 by the authors. Licensee MDPI, Basel, Switzerlanden_US
dc.subject.otherChagas diseaseen_US
dc.subject.otherLeishmania majoren_US
dc.subject.otherLeishmaniasisen_US
dc.subject.otherMolecular modellingen_US
dc.subject.otherSerodiagnosisen_US
dc.subject.otherTrypanosoma cruzien_US
dc.titleMolecular characterization of TC964, a novel antigenic protein from trypanosoma cruzien_US
dc.typearticleen
dc.subject.ecienciaBiología y Biomedicina / Biologíaes_ES
dc.relation.publisherversionhttps://dx.doi.org/10.3390/ijms21072432es_ES
dc.identifier.doi10.3390/ijms21072432es_ES
dc.identifier.publicationfirstpage2432-1es_ES
dc.identifier.publicationissue7es_ES
dc.identifier.publicationlastpage2432-19es_ES
dc.identifier.publicationvolume21es_ES
dc.relation.projectIDGobierno de España. RTC-2017-6494-1es_ES
dc.relation.projectIDGobierno de España. RTI2018-094434-B-I00es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.rights.ccReconocimientoes_ES
dc.rights.accessRightsopenAccesses_ES
dc.authorUAMRequena Rolania, José María (259327)
dc.facultadUAMFacultad de Ciencias
dc.institutoUAMCentro de Biología Molecular Severo Ochoa (CBMSO)


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