DNA Phase Behavior in the Presence of Oppositely Charged Surfactants

Detalhes bibliográficos
Autor(a) principal: Dias, Rita
Data de Publicação: 2000
Outros Autores: Mel'nikov, Sergey, Lindman, Björn, Miguel, Maria G.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/10329
https://doi.org/10.1021/la000640f
Resumo: The interaction between DNA and alkyltrimethylammonium bromides of various chain lengths has been investigated. It is known that these systems phase separate with the formation of a precipitate; this important feature allows, for example, purification of nucleic acids. Phase maps were drawn for the aqueous systems illustrating the associative phase separation. The boundary of the two-phase region for the dilute part of the phase diagram was evaluated by turbidimetry, in both the absence and presence of salt. The extension of the precipitate region increases strongly with the surfactant alkyl chain length, and we observed no redissolution with an excess of surfactant. The addition of NaBr led to novel interesting findings. The phase diagram studies were correlated with the single molecule conformational behavior of the same systems as studied for very diluted solutions by fluorescence microscopy. DNA exhibits a discrete phase transition in the presence of cationic surfactants from coils to globules. Results demonstrate that the coil−globule coexistence interval is narrow for CTAB and becomes wider for the shorter-chained surfactant. The findings for flexible polyions of lower charge density differ qualitatively from what we find here for DNA. For the first, large amounts of surfactant have to be added before phase separation occurs, and the change in the polyion extension is gradual, indicating an essentially uniform distribution of surfactant aggregates among the different polyions. For DNA, the very low values of surfactant concentration at which phase separation starts demonstrate a different binding interaction; as binding to a polyion starts, further binding is facilitated, and one DNA molecule is saturated before binding starts at another.
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spelling DNA Phase Behavior in the Presence of Oppositely Charged SurfactantsThe interaction between DNA and alkyltrimethylammonium bromides of various chain lengths has been investigated. It is known that these systems phase separate with the formation of a precipitate; this important feature allows, for example, purification of nucleic acids. Phase maps were drawn for the aqueous systems illustrating the associative phase separation. The boundary of the two-phase region for the dilute part of the phase diagram was evaluated by turbidimetry, in both the absence and presence of salt. The extension of the precipitate region increases strongly with the surfactant alkyl chain length, and we observed no redissolution with an excess of surfactant. The addition of NaBr led to novel interesting findings. The phase diagram studies were correlated with the single molecule conformational behavior of the same systems as studied for very diluted solutions by fluorescence microscopy. DNA exhibits a discrete phase transition in the presence of cationic surfactants from coils to globules. Results demonstrate that the coil−globule coexistence interval is narrow for CTAB and becomes wider for the shorter-chained surfactant. The findings for flexible polyions of lower charge density differ qualitatively from what we find here for DNA. For the first, large amounts of surfactant have to be added before phase separation occurs, and the change in the polyion extension is gradual, indicating an essentially uniform distribution of surfactant aggregates among the different polyions. For DNA, the very low values of surfactant concentration at which phase separation starts demonstrate a different binding interaction; as binding to a polyion starts, further binding is facilitated, and one DNA molecule is saturated before binding starts at another.American Chemical Society2000-11-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/10329http://hdl.handle.net/10316/10329https://doi.org/10.1021/la000640fengLangmuir. 16:24 (2000) 9577-95830743-7463Dias, RitaMel'nikov, SergeyLindman, BjörnMiguel, Maria G.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:RCAAP2020-02-11T18:17:31Zoai:estudogeral.uc.pt:10316/10329Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:12.957637Repositório 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 Phase Behavior in the Presence of Oppositely Charged Surfactants
title DNA Phase Behavior in the Presence of Oppositely Charged Surfactants
spellingShingle DNA Phase Behavior in the Presence of Oppositely Charged Surfactants
Dias, Rita
title_short DNA Phase Behavior in the Presence of Oppositely Charged Surfactants
title_full DNA Phase Behavior in the Presence of Oppositely Charged Surfactants
title_fullStr DNA Phase Behavior in the Presence of Oppositely Charged Surfactants
title_full_unstemmed DNA Phase Behavior in the Presence of Oppositely Charged Surfactants
title_sort DNA Phase Behavior in the Presence of Oppositely Charged Surfactants
author Dias, Rita
author_facet Dias, Rita
Mel'nikov, Sergey
Lindman, Björn
Miguel, Maria G.
author_role author
author2 Mel'nikov, Sergey
Lindman, Björn
Miguel, Maria G.
author2_role author
author
author
dc.contributor.author.fl_str_mv Dias, Rita
Mel'nikov, Sergey
Lindman, Björn
Miguel, Maria G.
description The interaction between DNA and alkyltrimethylammonium bromides of various chain lengths has been investigated. It is known that these systems phase separate with the formation of a precipitate; this important feature allows, for example, purification of nucleic acids. Phase maps were drawn for the aqueous systems illustrating the associative phase separation. The boundary of the two-phase region for the dilute part of the phase diagram was evaluated by turbidimetry, in both the absence and presence of salt. The extension of the precipitate region increases strongly with the surfactant alkyl chain length, and we observed no redissolution with an excess of surfactant. The addition of NaBr led to novel interesting findings. The phase diagram studies were correlated with the single molecule conformational behavior of the same systems as studied for very diluted solutions by fluorescence microscopy. DNA exhibits a discrete phase transition in the presence of cationic surfactants from coils to globules. Results demonstrate that the coil−globule coexistence interval is narrow for CTAB and becomes wider for the shorter-chained surfactant. The findings for flexible polyions of lower charge density differ qualitatively from what we find here for DNA. For the first, large amounts of surfactant have to be added before phase separation occurs, and the change in the polyion extension is gradual, indicating an essentially uniform distribution of surfactant aggregates among the different polyions. For DNA, the very low values of surfactant concentration at which phase separation starts demonstrate a different binding interaction; as binding to a polyion starts, further binding is facilitated, and one DNA molecule is saturated before binding starts at another.
publishDate 2000
dc.date.none.fl_str_mv 2000-11-28
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/10329
http://hdl.handle.net/10316/10329
https://doi.org/10.1021/la000640f
url http://hdl.handle.net/10316/10329
https://doi.org/10.1021/la000640f
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Langmuir. 16:24 (2000) 9577-9583
0743-7463
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dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
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