DNA−Surfactant Complexes at Solid Surfaces

Detalhes bibliográficos
Autor(a) principal: Eskilsson, K.
Data de Publicação: 2001
Outros Autores: Leal, C., Lindman, B., Miguel, M., Nylander, T.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10625
https://doi.org/10.1021/la000993e
Resumo: In this work, we report on the adsorption of complexes between DNA of different molecular weight and a cationic surfactant, cetyltrimethylammonium bromide (CTAB), on hydrophobized and hydrophilic negatively charged silica surfaces as measured by ellipsometry. We will demonstrate how the adsorption is affected by the state of the DNA−surfactant complexes formed in bulk solution. High molecular weight DNA molecules, which condense (transform from coil to globule state) on addition of small amounts of cationic surfactants, do not adsorb on hydrophilic silica prior to phase separation. However, DNA−surfactant complexes formed from low molecular weight DNA were found to adsorb. For these complexes surfactants interact with DNA, without condensation of the DNA. Adsorbed DNA−surfactant complexes can easily be removed from the hydrophilic silica surface when replacing the bulk DNA−surfactant solution with pure salt solution. At the hydrophobic surface the DNA adsorbs without addition of cationic surfactant. However, with addition of a very low amount of surfactant, a rapid increase in adsorbed amount and a simultaneous decrease in adsorbed layer thickness are observed. This compaction of the adsorbed layer is to some extent reversible when replacing the bulk DNA−surfactant solution with pure salt solution.
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spelling DNA−Surfactant Complexes at Solid SurfacesIn this work, we report on the adsorption of complexes between DNA of different molecular weight and a cationic surfactant, cetyltrimethylammonium bromide (CTAB), on hydrophobized and hydrophilic negatively charged silica surfaces as measured by ellipsometry. We will demonstrate how the adsorption is affected by the state of the DNA−surfactant complexes formed in bulk solution. High molecular weight DNA molecules, which condense (transform from coil to globule state) on addition of small amounts of cationic surfactants, do not adsorb on hydrophilic silica prior to phase separation. However, DNA−surfactant complexes formed from low molecular weight DNA were found to adsorb. For these complexes surfactants interact with DNA, without condensation of the DNA. Adsorbed DNA−surfactant complexes can easily be removed from the hydrophilic silica surface when replacing the bulk DNA−surfactant solution with pure salt solution. At the hydrophobic surface the DNA adsorbs without addition of cationic surfactant. However, with addition of a very low amount of surfactant, a rapid increase in adsorbed amount and a simultaneous decrease in adsorbed layer thickness are observed. This compaction of the adsorbed layer is to some extent reversible when replacing the bulk DNA−surfactant solution with pure salt solution.American Chemical Society2001-03-06info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10625http://hdl.handle.net/10316/10625https://doi.org/10.1021/la000993eengLangmuir. 17:5 (2001) 1666-16690743-7463Eskilsson, K.Leal, C.Lindman, B.Miguel, M.Nylander, T.info: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:RCAAP2020-03-05T10:56:24Zoai:estudogeral.uc.pt:10316/10625Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:34.108249Repositório 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 DNA−Surfactant Complexes at Solid Surfaces
title DNA−Surfactant Complexes at Solid Surfaces
spellingShingle DNA−Surfactant Complexes at Solid Surfaces
Eskilsson, K.
title_short DNA−Surfactant Complexes at Solid Surfaces
title_full DNA−Surfactant Complexes at Solid Surfaces
title_fullStr DNA−Surfactant Complexes at Solid Surfaces
title_full_unstemmed DNA−Surfactant Complexes at Solid Surfaces
title_sort DNA−Surfactant Complexes at Solid Surfaces
author Eskilsson, K.
author_facet Eskilsson, K.
Leal, C.
Lindman, B.
Miguel, M.
Nylander, T.
author_role author
author2 Leal, C.
Lindman, B.
Miguel, M.
Nylander, T.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Eskilsson, K.
Leal, C.
Lindman, B.
Miguel, M.
Nylander, T.
description In this work, we report on the adsorption of complexes between DNA of different molecular weight and a cationic surfactant, cetyltrimethylammonium bromide (CTAB), on hydrophobized and hydrophilic negatively charged silica surfaces as measured by ellipsometry. We will demonstrate how the adsorption is affected by the state of the DNA−surfactant complexes formed in bulk solution. High molecular weight DNA molecules, which condense (transform from coil to globule state) on addition of small amounts of cationic surfactants, do not adsorb on hydrophilic silica prior to phase separation. However, DNA−surfactant complexes formed from low molecular weight DNA were found to adsorb. For these complexes surfactants interact with DNA, without condensation of the DNA. Adsorbed DNA−surfactant complexes can easily be removed from the hydrophilic silica surface when replacing the bulk DNA−surfactant solution with pure salt solution. At the hydrophobic surface the DNA adsorbs without addition of cationic surfactant. However, with addition of a very low amount of surfactant, a rapid increase in adsorbed amount and a simultaneous decrease in adsorbed layer thickness are observed. This compaction of the adsorbed layer is to some extent reversible when replacing the bulk DNA−surfactant solution with pure salt solution.
publishDate 2001
dc.date.none.fl_str_mv 2001-03-06
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/10316/10625
http://hdl.handle.net/10316/10625
https://doi.org/10.1021/la000993e
url http://hdl.handle.net/10316/10625
https://doi.org/10.1021/la000993e
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Langmuir. 17:5 (2001) 1666-1669
0743-7463
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
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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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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