Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/001300000tdd5 |
Texto Completo: | http://dx.doi.org/10.1016/j.femsle.2004.04.040 http://repositorio.unifesp.br/handle/11600/27792 |
Resumo: | B13, one of the immunodominant antigens of Trypanosoma cruzi, is composed of repeats of a 12-amino-acid motif. Using synthetic peptides, the sequence FGQAAAGDK was previously shown to contain the B13 immunodominant epitope recognized by chagasic patients sera. To investigate the effects of neighboring sequences in the immunodominance, we tested serum recognition of two B13 sequences fused to LamB. GDKPSPFGQAAA-LamB and FGQAAAGDKPSP-LamB were recognized, respectively, by 15% and 80% of 80 sera reactive to B13 antigen. Recognition of FGQAAAGDKPSP-LamB was inhibited by AAAGDK-containing synthetic peptides. FGQAAAGDKPSP-LamB competed with a B13 recombinant protein containing 16.6 repeats for binding to chagasic antibodies. These results strengthen previous conclusions on the immunodominant epitope of B13 and provide a comparison of two methods for epitope mapping. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Microbiological Societies. |
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Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB proteinTrypanosoma cruziimmunodominant repetitive antigenB13 antigenB cell epitope mappingEscherichia coli LamB proteinB13, one of the immunodominant antigens of Trypanosoma cruzi, is composed of repeats of a 12-amino-acid motif. Using synthetic peptides, the sequence FGQAAAGDK was previously shown to contain the B13 immunodominant epitope recognized by chagasic patients sera. To investigate the effects of neighboring sequences in the immunodominance, we tested serum recognition of two B13 sequences fused to LamB. GDKPSPFGQAAA-LamB and FGQAAAGDKPSP-LamB were recognized, respectively, by 15% and 80% of 80 sera reactive to B13 antigen. Recognition of FGQAAAGDKPSP-LamB was inhibited by AAAGDK-containing synthetic peptides. FGQAAAGDKPSP-LamB competed with a B13 recombinant protein containing 16.6 repeats for binding to chagasic antibodies. These results strengthen previous conclusions on the immunodominant epitope of B13 and provide a comparison of two methods for epitope mapping. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Microbiological Societies.UNIFESP, Escola Paulista Med, Dept Microbiol Immunol & Parasitol, BR-01023062 São Paulo, BrazilUniv São Paulo, Inst Quim, Dept Bioquim, BR-01498 São Paulo, BrazilUniv São Paulo, Fac Med, Inst Coracao, Lab Immunol Transplantes, BR-01498 São Paulo, BrazilUNIFESP, Escola Paulista Med, Dept Microbiol Immunol & Parasitol, BR-01023062 São Paulo, BrazilWeb of ScienceElsevier B.V.Universidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Pereira, Catia Mendes [UNIFESP]Franco da Silveira, José [UNIFESP]Duranti, M.Cunha-Neto, E.Zingales, B.Castilho, Beatriz Amaral de [UNIFESP]2016-01-24T12:37:12Z2016-01-24T12:37:12Z2004-06-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion237-242http://dx.doi.org/10.1016/j.femsle.2004.04.040Fems Microbiology Letters. Amsterdam: Elsevier B.V., v. 235, n. 2, p. 237-242, 2004.10.1016/j.femsle.2004.04.0400378-1097http://repositorio.unifesp.br/handle/11600/27792WOS:000222144400004ark:/48912/001300000tdd5engFems Microbiology Lettersinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2022-02-08T11:55:01Zoai:repositorio.unifesp.br/:11600/27792Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T20:37:17.507870Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein |
title |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein |
spellingShingle |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein Pereira, Catia Mendes [UNIFESP] Trypanosoma cruzi immunodominant repetitive antigen B13 antigen B cell epitope mapping Escherichia coli LamB protein |
title_short |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein |
title_full |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein |
title_fullStr |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein |
title_full_unstemmed |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein |
title_sort |
Epitope mapping of a single repetitive unit of the B13 Trypanosoma cruzi antigen as fusions to Escherichia coli LamB protein |
author |
Pereira, Catia Mendes [UNIFESP] |
author_facet |
Pereira, Catia Mendes [UNIFESP] Franco da Silveira, José [UNIFESP] Duranti, M. Cunha-Neto, E. Zingales, B. Castilho, Beatriz Amaral de [UNIFESP] |
author_role |
author |
author2 |
Franco da Silveira, José [UNIFESP] Duranti, M. Cunha-Neto, E. Zingales, B. Castilho, Beatriz Amaral de [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Pereira, Catia Mendes [UNIFESP] Franco da Silveira, José [UNIFESP] Duranti, M. Cunha-Neto, E. Zingales, B. Castilho, Beatriz Amaral de [UNIFESP] |
dc.subject.por.fl_str_mv |
Trypanosoma cruzi immunodominant repetitive antigen B13 antigen B cell epitope mapping Escherichia coli LamB protein |
topic |
Trypanosoma cruzi immunodominant repetitive antigen B13 antigen B cell epitope mapping Escherichia coli LamB protein |
description |
B13, one of the immunodominant antigens of Trypanosoma cruzi, is composed of repeats of a 12-amino-acid motif. Using synthetic peptides, the sequence FGQAAAGDK was previously shown to contain the B13 immunodominant epitope recognized by chagasic patients sera. To investigate the effects of neighboring sequences in the immunodominance, we tested serum recognition of two B13 sequences fused to LamB. GDKPSPFGQAAA-LamB and FGQAAAGDKPSP-LamB were recognized, respectively, by 15% and 80% of 80 sera reactive to B13 antigen. Recognition of FGQAAAGDKPSP-LamB was inhibited by AAAGDK-containing synthetic peptides. FGQAAAGDKPSP-LamB competed with a B13 recombinant protein containing 16.6 repeats for binding to chagasic antibodies. These results strengthen previous conclusions on the immunodominant epitope of B13 and provide a comparison of two methods for epitope mapping. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Microbiological Societies. |
publishDate |
2004 |
dc.date.none.fl_str_mv |
2004-06-15 2016-01-24T12:37:12Z 2016-01-24T12:37:12Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.femsle.2004.04.040 Fems Microbiology Letters. Amsterdam: Elsevier B.V., v. 235, n. 2, p. 237-242, 2004. 10.1016/j.femsle.2004.04.040 0378-1097 http://repositorio.unifesp.br/handle/11600/27792 WOS:000222144400004 |
dc.identifier.dark.fl_str_mv |
ark:/48912/001300000tdd5 |
url |
http://dx.doi.org/10.1016/j.femsle.2004.04.040 http://repositorio.unifesp.br/handle/11600/27792 |
identifier_str_mv |
Fems Microbiology Letters. Amsterdam: Elsevier B.V., v. 235, n. 2, p. 237-242, 2004. 10.1016/j.femsle.2004.04.040 0378-1097 WOS:000222144400004 ark:/48912/001300000tdd5 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Fems Microbiology Letters |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
dc.format.none.fl_str_mv |
237-242 |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1818602517069561856 |