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Synthetic DNA-compacting peptides derived from human sequence enhance cationic lipid-mediated gene transfer in vitro and in vivo

Gene Therapy volume 6, pages 282–292 (1999)Cite this article

Abstract

Cationic lipids can deliver genes efficiently in vitro, but are generally inhibited by the presence of serum, and their efficiency in vivo is much lower than in vitro. An attractive strategy is to induce strong DNA compaction by its association with proteins, before addition of lipids. However the use of whole proteins might present both production and immunological limitations. We have devised a system in which DNA is associated with short peptides derived from human histone or protamine, before the addition of a cationic lipid or polymer. Peptides strongly associating with DNA confer to such peptide–DNA–lipid particles an enhanced in vitro transfection efficiency over that observed with classical DNA/lipid lipoplexes, and particularly confer the capacity to transfect in the presence of serum. This acquisition of serum resistance is cell type-independent, and observed with all four lipopolyamines tested and polyethylenimine. Precompacting DNA with a histone H1-derived peptide enhances cationic lipid RPR 115335-mediated gene transfer in an in vivo model of Lewis lung carcinoma. Apart from their use in peptide–DNA–lipid association, such peptides could be useful as part of chimeric gene delivery vectors presenting a DNA-binding moiety that can be easily associated with other functional domains.

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Authors and Affiliations

  1. UMR 133 CNRS, Rhône-Poulenc Rorer Gencell, CRVA, Vitry/Seine, France

    B Schwartz, M-A Ivanov, B Pitard, V Escriou, R Rangara, G Byk, P Wils & D Scherman

  2. RPR, Gencell Vector Design, CRVA, Vitry/Seine, France

    J Crouzet

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  1. B Schwartz
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  2. M-A Ivanov
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  3. B Pitard
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  4. V Escriou
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Schwartz, B., Ivanov, MA., Pitard, B. et al. Synthetic DNA-compacting peptides derived from human sequence enhance cationic lipid-mediated gene transfer in vitro and in vivo. Gene Ther 6, 282–292 (1999). https://doi.org/10.1038/sj.gt.3300795

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  • DOI: https://doi.org/10.1038/sj.gt.3300795

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