The structure of novel spontaneously self-assembled plasmid DNA/lipid complexes is investigated by means of synchrotron radiation small-angle X-ray scattering (SAXS) and Cryo-TEM imaging. Liquid crystalline (LC) hydrated lipid systems are prepared using the non-ionic lipids monoolein and DOPE-PEG 2000 and the cationic amphiphile CTAB. The employed plasmid DNA (pDNA) is encoding for the human protein brain-derived neurotrophic factor (BDNF). A coexistence of nanoparticulate objects with different LC inner organizations is established. A transition from bicontinuous membrane sponges, cubosome intermediates and unilamelar liposomes to multilamellar vesicles, functionalized by pDNA, is favoured upon binding and compaction of pBDNF onto the cationic PEGylated lipid nanocarriers. The obtained sterically stabilized multicompartment nanoobjects, with confined supercoiled plasmid DNA (pBDNF), are important in the context of multicompartment lipid nanocarriers of interest for gene therapy of neurodegenerative diseases. © Published under licence by IOP Publishing Ltd.
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Angelov, B., Angelova, A., Filippov, S., Karlsson, G., Terrill, N., Lesieur, S., & Štěpánek, P. (2012). SAXS study of sterically stabilized lipid nanocarriers functionalized by DNA. In Journal of Physics: Conference Series (Vol. 351). Institute of Physics Publishing. https://doi.org/10.1088/1742-6596/351/1/012004