The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems

Detalhes bibliográficos
Autor(a) principal: Reyes, Luis Fernando
Data de Publicação: 2012
Outros Autores: Nobre, Thatyane Morimoto, Pavinatto, Felippe José, Zaniquelli, Maria Elisabete Darbello, Caseli, Luciano [UNIFESP], Oliveira, Osvaldo N., Araujo, Ana Paula Ulian
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.bbamem.2011.10.002
http://repositorio.unifesp.br/handle/11600/34337
Resumo: Pulchellin is a Ribosome Inactivating Protein containing an A-chain (PAC), whose toxic activity requires crossing the endoplasmic reticulum (ER) membrane. in this paper, we investigate the interaction between recombinant PAC (rPAC) and Langmuir monolayers of dipalmitoyl phosphatidyl glycerol (DPPG), which served as membrane model. Three catalytically active, truncated PACs with increasing deletion of the C-terminal region, possessing 244,239 and 236 residues (rPAC(244), rPAC(239) and rPAC(236)), were studied. rPAC had the strongest interaction with the DPPG monolayer, inducing a large expansion in its surface pressure-area isotherm. the affinity to DPPG decreased with increased deletion of the C-terminal region. When the C-terminal region was deleted completely (rPAC(236)), the interaction was recovered, probably because other hydrophobic regions were exposed to the membrane. Using Polarization Modulated-Infrared Reflection Absorption Spectroscopy (PM-IRRAS) we observed that at a bare air/water interface rPAC comprised mainly alpha-helix structures, the C-terminal region had unordered structures when interacting with DPPG. for rPAC(236) the alpha-helices were preserved even in the presence of DPPG. These results confirm the importance of the C-terminal region for PAC-ER membrane interaction. the partial unfolding only with preserved C-terminal appears a key step for the protein to reach the cytosol and develop its toxic activity. (C) 2011 Elsevier B.V. All rights reserved.
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spelling The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systemsRibosome inactivating proteinLangmuir monolayersPulchellinMembrane interactionPM-IRRASPulchellin is a Ribosome Inactivating Protein containing an A-chain (PAC), whose toxic activity requires crossing the endoplasmic reticulum (ER) membrane. in this paper, we investigate the interaction between recombinant PAC (rPAC) and Langmuir monolayers of dipalmitoyl phosphatidyl glycerol (DPPG), which served as membrane model. Three catalytically active, truncated PACs with increasing deletion of the C-terminal region, possessing 244,239 and 236 residues (rPAC(244), rPAC(239) and rPAC(236)), were studied. rPAC had the strongest interaction with the DPPG monolayer, inducing a large expansion in its surface pressure-area isotherm. the affinity to DPPG decreased with increased deletion of the C-terminal region. When the C-terminal region was deleted completely (rPAC(236)), the interaction was recovered, probably because other hydrophobic regions were exposed to the membrane. Using Polarization Modulated-Infrared Reflection Absorption Spectroscopy (PM-IRRAS) we observed that at a bare air/water interface rPAC comprised mainly alpha-helix structures, the C-terminal region had unordered structures when interacting with DPPG. for rPAC(236) the alpha-helices were preserved even in the presence of DPPG. These results confirm the importance of the C-terminal region for PAC-ER membrane interaction. the partial unfolding only with preserved C-terminal appears a key step for the protein to reach the cytosol and develop its toxic activity. (C) 2011 Elsevier B.V. All rights reserved.Univ São Paulo, Inst Fis Sao Carlos, Ctr Biotecnol Mol Estrut, BR-13560970 Sao Carlos, SP, BrazilUniv São Paulo, Inst Fis Sao Carlos, Grp Polimeros Bernhard Gross, BR-13560970 Sao Carlos, SP, BrazilUniv São Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Quim, BR-14049 Ribeirao Preto, SP, BrazilUniversidade Federal de São Paulo, Inst Ciencias Ambientais Quim & Farmaceut, Diadema, SP, BrazilUniversidade Federal de São Paulo, Inst Ciencias Ambientais Quim & Farmaceut, Diadema, SP, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Elsevier B.V.Universidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Reyes, Luis FernandoNobre, Thatyane MorimotoPavinatto, Felippe JoséZaniquelli, Maria Elisabete DarbelloCaseli, Luciano [UNIFESP]Oliveira, Osvaldo N.Araujo, Ana Paula Ulian2016-01-24T14:17:35Z2016-01-24T14:17:35Z2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion82-89application/pdfhttp://dx.doi.org/10.1016/j.bbamem.2011.10.002Biochimica Et Biophysica Acta-biomembranes. Amsterdam: Elsevier B.V., v. 1818, n. 1, p. 82-89, 2012.10.1016/j.bbamem.2011.10.002WOS000298461100011.pdf0005-2736http://repositorio.unifesp.br/handle/11600/34337WOS:000298461100011engBiochimica Et Biophysica Acta-biomembranesinfo: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:UNIFESP2024-07-31T23:08:50Zoai:repositorio.unifesp.br/:11600/34337Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-31T23:08:50Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
title The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
spellingShingle The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
Reyes, Luis Fernando
Ribosome inactivating protein
Langmuir monolayers
Pulchellin
Membrane interaction
PM-IRRAS
title_short The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
title_full The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
title_fullStr The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
title_full_unstemmed The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
title_sort The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
author Reyes, Luis Fernando
author_facet Reyes, Luis Fernando
Nobre, Thatyane Morimoto
Pavinatto, Felippe José
Zaniquelli, Maria Elisabete Darbello
Caseli, Luciano [UNIFESP]
Oliveira, Osvaldo N.
Araujo, Ana Paula Ulian
author_role author
author2 Nobre, Thatyane Morimoto
Pavinatto, Felippe José
Zaniquelli, Maria Elisabete Darbello
Caseli, Luciano [UNIFESP]
Oliveira, Osvaldo N.
Araujo, Ana Paula Ulian
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Reyes, Luis Fernando
Nobre, Thatyane Morimoto
Pavinatto, Felippe José
Zaniquelli, Maria Elisabete Darbello
Caseli, Luciano [UNIFESP]
Oliveira, Osvaldo N.
Araujo, Ana Paula Ulian
dc.subject.por.fl_str_mv Ribosome inactivating protein
Langmuir monolayers
Pulchellin
Membrane interaction
PM-IRRAS
topic Ribosome inactivating protein
Langmuir monolayers
Pulchellin
Membrane interaction
PM-IRRAS
description Pulchellin is a Ribosome Inactivating Protein containing an A-chain (PAC), whose toxic activity requires crossing the endoplasmic reticulum (ER) membrane. in this paper, we investigate the interaction between recombinant PAC (rPAC) and Langmuir monolayers of dipalmitoyl phosphatidyl glycerol (DPPG), which served as membrane model. Three catalytically active, truncated PACs with increasing deletion of the C-terminal region, possessing 244,239 and 236 residues (rPAC(244), rPAC(239) and rPAC(236)), were studied. rPAC had the strongest interaction with the DPPG monolayer, inducing a large expansion in its surface pressure-area isotherm. the affinity to DPPG decreased with increased deletion of the C-terminal region. When the C-terminal region was deleted completely (rPAC(236)), the interaction was recovered, probably because other hydrophobic regions were exposed to the membrane. Using Polarization Modulated-Infrared Reflection Absorption Spectroscopy (PM-IRRAS) we observed that at a bare air/water interface rPAC comprised mainly alpha-helix structures, the C-terminal region had unordered structures when interacting with DPPG. for rPAC(236) the alpha-helices were preserved even in the presence of DPPG. These results confirm the importance of the C-terminal region for PAC-ER membrane interaction. the partial unfolding only with preserved C-terminal appears a key step for the protein to reach the cytosol and develop its toxic activity. (C) 2011 Elsevier B.V. All rights reserved.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01
2016-01-24T14:17:35Z
2016-01-24T14:17:35Z
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.bbamem.2011.10.002
Biochimica Et Biophysica Acta-biomembranes. Amsterdam: Elsevier B.V., v. 1818, n. 1, p. 82-89, 2012.
10.1016/j.bbamem.2011.10.002
WOS000298461100011.pdf
0005-2736
http://repositorio.unifesp.br/handle/11600/34337
WOS:000298461100011
url http://dx.doi.org/10.1016/j.bbamem.2011.10.002
http://repositorio.unifesp.br/handle/11600/34337
identifier_str_mv Biochimica Et Biophysica Acta-biomembranes. Amsterdam: Elsevier B.V., v. 1818, n. 1, p. 82-89, 2012.
10.1016/j.bbamem.2011.10.002
WOS000298461100011.pdf
0005-2736
WOS:000298461100011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biochimica Et Biophysica Acta-biomembranes
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 82-89
application/pdf
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
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