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The ionic strength effect on the DNA complexation by DOPC - gemini surfactants liposomes
Authors:Pullmannová Petra  Bastos Margarida  Bai Guangyue  Funari Sergio S  Lacko Ivan  Devínsky Ferdinand  Teixeira José  Uhríková Daniela
Affiliation:
  • a Department of Physical Chemistry, Faculty of Chemical and Food Technology, Slovak University of Technology, Radlinského 9, SK-812 37 Bratislava, Slovakia
  • b Department of Physical Chemistry of Drugs, Faculty of Pharmacy, Comenius University, Odbojárov 10, SK-832 32 Bratislava, Slovakia
  • c CIQ(UP), Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Rua do Campo Alegre 687, P-4169-007, Porto, Portugal
  • d HASYLAB at DESY, Notkestr. 85, D-22607 Hamburg, Germany
  • e Department of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University, Odbojárov 10, SK-832 32 Bratislava, Slovakia
  • f Laboratoire Léon Brillouin (CEA-CNRS), CEA Saclay, F-91191 Gif-sur-Yvette Cedex, France
  • Abstract:Liposome dispersions obtained from the mixture of gemini surfactants of the type alkane-α,ω-diyl-bis(alkyldimethylammonium bromide) and helper lipid DOPC create complexes with DNA showing a regular inner microstructure, identified by small angle X-ray diffraction as condensed lamellar phase (Lαc). In addition to the Lαc phase, a coexisting lamellar phase LB was also identified in the complexes formed, with periodicities in the range ~ 8.8-5.7 nm, at ionic strengths corresponding to 50-200 mM NaCl. The periodicities of LB phase did not correspond to those identified in liposome dispersion without DNA using small angle neutron scattering. The observed phase separation is shown to depend on the interplay between the surface charge density of cationic liposomes, ionic strength and method of complex preparation. The effect of ionic strength on complex formation was studied by isothermal titration calorimetry and zeta potential measurements. High ionic strength reduces the fraction of bound DNA in the complexes, and the isoelectric point is attained at a ratio of DNA/gemini surfactant which is lower than the one that can be estimated by calculation based on nominal charges of CLs and DNA.
    Keywords:CLs, cationic liposomes   CnGSm, gemini surfactant alkane-α,ω-diyl-bis(alkyldimethylammonium bromide)   DOPC, dioleylphosphatidylcholine   DPPC, dipalmitoylphosphatidylcholine   CTDNA, calf thymus DNA   HTDNA, DNA from herring testes   Lαc, condensed lamellar phase   LB, additional lipid phase with lamellar structure   SAXD, small angle X-ray diffraction   WAXD, wide angle X-ray diffraction   SANS, small angle neutron scattering   ITC, isothermal titration calorimetry
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