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|Title:||Structure and internal organization of overcharged cationic-lipid/peptide/DNA self-assembly complexes||Authors:||Yan, Jiang
Berezhnoy, Nikolay V.
|Keywords:||DRNTU::Science::Biological sciences||Issue Date:||2012||Source:||Yan, J., Berezhnoy, N. V., Korolev, N., Su, C. J.,& Nordenskiöld, L. (2012). Structure and internal organization of overcharged cationic-lipid/peptide/DNA self-assembly complexes. Biochimica et Biophysica Acta (BBA) - Biomembranes, 1818(7), 1794-1800.||Series/Report no.:||Biochimica et Biophysica Acta (BBA) - biomembranes||Abstract:||The combination of cationic lipids with cationic peptides and DNA vectors can produce synergistic effects in gene delivery to eukaryotic cells. Binary complexes of cationic lipids with DNA are well-studied whereas little information is available about the structure of the ternary lipid/peptide/DNA (LPD) complexes and mechanisms defining DNA protection and delivery. Here we use synchrotron small angle X-ray scattering and dynamic light scattering zeta-potential measurements to determine structure and the net charge of supramolecular aggregates of complexes in mixtures of plasmid DNA, cationic liposomes formed from DOTAP, plus a linear cationic ε-oligolysine with the pendant α-amino acids Leu-Tyr-Arg (LYR), ε-(LYR)K10. These ternary complexes display multilamellar structures with relatively constant separation between DOTAP bilayers, accommodating a hydrated monolayer of parallel DNA rods. The DNA–DNA distance in the complexes varies as a function of the net positive to negative (lipid + peptide)/DNA charge ratio. An explanation for the observed dependence of DNA–DNA distance on charge ratio was proposed based on general polyelectrolyte properties of non-stoichiometric polycation–DNA mixtures.||URI:||https://hdl.handle.net/10356/98791
|ISSN:||0005-2736||DOI:||10.1016/j.bbamem.2012.03.022||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SBS Journal Articles|
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