Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98791
Title: Structure and internal organization of overcharged cationic-lipid/peptide/DNA self-assembly complexes
Authors: Yan, Jiang
Korolev, Nikolay
Su, Chun-Jen
Nordenskiöld, Lars
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
http://hdl.handle.net/10220/12747
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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