Cellular uptake of self-assembled cationic peptide-DNA complexes

multifunctional role of the enhancer chloroquine

Shu Yang, Daniel J. Coles, Anna Esposito, Deanne J. Mitchell, Istvan Toth, Rodney F. Minchin

Research output: Contribution to journalArticle

63 Citations (Scopus)

Abstract

A small library of carriers consisting of various combinations of the cell penetrating peptide TAT, the SV40 Large T protein nuclear localisation signal (NLS) and a cationic dendrimer of 7 lysine residues (DEN) was synthesised and each member was tested for its ability to deliver exogenous DNA to human HeLa cells. We found that the TAT peptide was essential, but not sufficient for efficient uptake of exogenous DNA. The addition of either NLS or DEN significantly enhanced uptake and expression with the most active carrier consisting of the TAT, NLS and DEN peptides. For those peptides that facilitated DNA uptake, the complexes were targeted to intracellular compartments that required incubation with a fusogenic agent such as chloroquine before gene expression was observed. However, our data suggest that chloroquine did not enhance expression solely by promoting endosomal release since a fusogenic peptide derived from the influenza virus haemagglutinin protein did not improve gene expression. Chloroquine was found to protect DNA from degradation and enhance transcription of DNA bound to the respective carriers. Our results demonstrate that multi-component peptide-based gene carriers can be designed to deliver exogenous DNA. The actions of lysosomotropic agents such as chloroquine reveal the multifactorial properties required for carriers used in non-viral gene delivery.
Original languageEnglish
Pages (from-to)159-165
Number of pages7
JournalJournal of Controlled Release
Volume135
Issue number2
DOIs
Publication statusPublished - 2009
Externally publishedYes

Keywords

  • Cell penetrating peptide
  • Gene delivery
  • Peptide-based carriers

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