The role of the C-terminal region of pulchellin A-chain in the interaction with membrane model systems
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1814268341822423040 |