What is it about?

In this paper we assess the capacity of three fusogenic peptides to promote the endosomal escape of a multicomponent gene delivery system incorporating a cell penetrating peptide [TAT(48-60)] to improve cellular uptake, a cationic poly-L-lysine dendron to condense DNA, and a library of different fusogenic endosome escape peptides [GALA, KALA, HA2(1-20)] to assess their capacity to improve endosome escape and how this affects cell uptake, and toxicity.

Featured Image

Why is it important?

Gene therapy is an exciting means to treat or prevent numerous diseases. Safety issues associated with viral gene delivery vectors have led to interest in non-viral approaches. However, this approach faces numerous barriers to its success, with escape from endosomes after the cellular uptake of such systems representing one of the major barriers to non-viral gene delivery. This paper provides important information about the efficacy and issues associated with the use of various endosome escape peptides.

Perspectives

This paper provides important information to researchers about how to incorporate fusogenic endosome escape peptides into multicomponent gene delivery systems (we developed a CuAAC-based chemical technique), and provides valuable information about the efficacy of each of these peptides, including their effects on cellular uptake and toxicity.

Dr Peter Michael Moyle
University of Queensland

Read the Original

This page is a summary of: Nanosized, peptide-based multicomponent DNA delivery systems: optimization of endosome escape activity, Nanomedicine, April 2016, Future Medicine, DOI: 10.2217/nnm.16.27.
You can read the full text:

Read

Contributors

The following have contributed to this page