Human-derived NLS enhance the gene transfer efficiency of chitosan

Detalhes bibliográficos
Autor(a) principal: Bitoque, Diogo
Data de Publicação: 2021
Outros Autores: Morais, Joana, Oliveira, Ana, Sequeira, Raquel L., Calado, Sofia, Fortunato, Tiago M., Simão, Sónia, Rosa Da Costa, Ana, Silva, Gabriela A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.1/15393
Resumo: Nuclear import is considered as one of the major limitations for non-viral gene delivery systems and the incorporation of nuclear localization signals (NLS) that mediate nuclear intake can be used as a strategy to enhance internalization of exogenous DNA. In this work, human-derived endogenous NLS peptides based on insulin growth factor binding proteins (IGFBP), namely IGFBP-3 and IGFBP-5, were tested for their ability to improve nuclear translocation of genetic material by non-viral vectors. Several strategies were tested to determine their effect on chitosan mediated transfection efficiency: co-administration with polyplexes, co-complexation at the time of polyplex formation, and covalent ligation to chitosan. Our results show that co-complexation and covalent ligation of the NLS peptide derived from IGFBP-3 to chitosan polyplexes yields a 2-fold increase in transfection efficiency, which was not observed for NLS peptide derived from IGFBP-5. These results indicate that the integration of IGFBP-NLS-3 peptides into polyplexes has potential as a strategy to enhance the efficiency of non-viral vectors.
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spelling Human-derived NLS enhance the gene transfer efficiency of chitosanNuclear import is considered as one of the major limitations for non-viral gene delivery systems and the incorporation of nuclear localization signals (NLS) that mediate nuclear intake can be used as a strategy to enhance internalization of exogenous DNA. In this work, human-derived endogenous NLS peptides based on insulin growth factor binding proteins (IGFBP), namely IGFBP-3 and IGFBP-5, were tested for their ability to improve nuclear translocation of genetic material by non-viral vectors. Several strategies were tested to determine their effect on chitosan mediated transfection efficiency: co-administration with polyplexes, co-complexation at the time of polyplex formation, and covalent ligation to chitosan. Our results show that co-complexation and covalent ligation of the NLS peptide derived from IGFBP-3 to chitosan polyplexes yields a 2-fold increase in transfection efficiency, which was not observed for NLS peptide derived from IGFBP-5. These results indicate that the integration of IGFBP-NLS-3 peptides into polyplexes has potential as a strategy to enhance the efficiency of non-viral vectors.FCT: PTDC/BTM/ORG/28121/2017; PD/BD/52424/2013; SFRH/BD/76873/2011;PIRG-GA-2009-249314Portland PressSapientiaBitoque, DiogoMorais, JoanaOliveira, AnaSequeira, Raquel L.Calado, SofiaFortunato, Tiago M.Simão, SóniaRosa Da Costa, AnaSilva, Gabriela A.2021-04-15T17:37:06Z20212021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/15393eng0144-846310.1042/BSR20201026info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-24T10:27:49Zoai:sapientia.ualg.pt:10400.1/15393Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:06:14.067478Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Human-derived NLS enhance the gene transfer efficiency of chitosan
title Human-derived NLS enhance the gene transfer efficiency of chitosan
spellingShingle Human-derived NLS enhance the gene transfer efficiency of chitosan
Bitoque, Diogo
title_short Human-derived NLS enhance the gene transfer efficiency of chitosan
title_full Human-derived NLS enhance the gene transfer efficiency of chitosan
title_fullStr Human-derived NLS enhance the gene transfer efficiency of chitosan
title_full_unstemmed Human-derived NLS enhance the gene transfer efficiency of chitosan
title_sort Human-derived NLS enhance the gene transfer efficiency of chitosan
author Bitoque, Diogo
author_facet Bitoque, Diogo
Morais, Joana
Oliveira, Ana
Sequeira, Raquel L.
Calado, Sofia
Fortunato, Tiago M.
Simão, Sónia
Rosa Da Costa, Ana
Silva, Gabriela A.
author_role author
author2 Morais, Joana
Oliveira, Ana
Sequeira, Raquel L.
Calado, Sofia
Fortunato, Tiago M.
Simão, Sónia
Rosa Da Costa, Ana
Silva, Gabriela A.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Sapientia
dc.contributor.author.fl_str_mv Bitoque, Diogo
Morais, Joana
Oliveira, Ana
Sequeira, Raquel L.
Calado, Sofia
Fortunato, Tiago M.
Simão, Sónia
Rosa Da Costa, Ana
Silva, Gabriela A.
description Nuclear import is considered as one of the major limitations for non-viral gene delivery systems and the incorporation of nuclear localization signals (NLS) that mediate nuclear intake can be used as a strategy to enhance internalization of exogenous DNA. In this work, human-derived endogenous NLS peptides based on insulin growth factor binding proteins (IGFBP), namely IGFBP-3 and IGFBP-5, were tested for their ability to improve nuclear translocation of genetic material by non-viral vectors. Several strategies were tested to determine their effect on chitosan mediated transfection efficiency: co-administration with polyplexes, co-complexation at the time of polyplex formation, and covalent ligation to chitosan. Our results show that co-complexation and covalent ligation of the NLS peptide derived from IGFBP-3 to chitosan polyplexes yields a 2-fold increase in transfection efficiency, which was not observed for NLS peptide derived from IGFBP-5. These results indicate that the integration of IGFBP-NLS-3 peptides into polyplexes has potential as a strategy to enhance the efficiency of non-viral vectors.
publishDate 2021
dc.date.none.fl_str_mv 2021-04-15T17:37:06Z
2021
2021-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.1/15393
url http://hdl.handle.net/10400.1/15393
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0144-8463
10.1042/BSR20201026
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Portland Press
publisher.none.fl_str_mv Portland Press
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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