Aggregation behavior and thermodynamics of binding between poly(ethylene oxide)-block-poly(2-(diethylamino)ethyl methacrylate) and plasmid DNA

The aggregation behavior and the thermodynamics of binding between poly(ethylene oxide)-block-poly(2-(diethylamino)ethyl methacrylate) (PEO-b-PDEAEMA) block copolymers and plasmid DNA were examined. Binding between the polymer and DNA were confirmed by gel electrophoresis. The high affinity between...

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Publié dans:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 22(2006), 8 vom: 11. Apr., Seite 3744-50
Auteur principal: Tan, J F (Auteur)
Autres auteurs: Too, H P, Hatton, T A, Tam, K C
Format: Article
Langue:English
Publié: 2006
Accès à la collection:Langmuir : the ACS journal of surfaces and colloids
Sujets:Journal Article Research Support, Non-U.S. Gov't Methacrylates Nylons Polymers poly(2-(diethylamino)ethyl methacrylate) Polyethylene Glycols 3WJQ0SDW1A DNA 9007-49-2 plus... Ethidium EN464416SI
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Résumé:The aggregation behavior and the thermodynamics of binding between poly(ethylene oxide)-block-poly(2-(diethylamino)ethyl methacrylate) (PEO-b-PDEAEMA) block copolymers and plasmid DNA were examined. Binding between the polymer and DNA were confirmed by gel electrophoresis. The high affinity between the polymer and DNA was demonstrated through the ethidium bromide (EtBr) displacement assay, and the binding was found to be related to the stoichiometric balance between the amine group of the polymer and the DNA nucleotide molar ratio (N/P molar ratio). The light scattering and TEM results showed that, at low polymer concentration, the hydrodynamic radii (R(h)) of the polymer/DNA complexes was around 90 nm; however, at sufficiently high polymer concentration, the complexes condensed to around 35 nm induced by a structural rearrangement of the amphiphilic nature of the block copolymer. The isothermal titration calorimetric results showed that the binding between the polymer and DNA is driven by a large favorable enthalpy
Description:Date Completed 09.07.2007
Date Revised 01.12.2018
published: Print
Citation Status MEDLINE
ISSN:1520-5827