4.7 Review

Peptide-mediated DNA condensation for non-viral gene therapy

Journal

BIOTECHNOLOGY ADVANCES
Volume 27, Issue 4, Pages 432-438

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.biotechadv.2009.03.004

Keywords

Recombinant drugs; Gene therapy; Protein engineering; Multifunctional proteins; Cationic peptides; DNA binding; Nanoparticles; Artificial viruses

Funding

  1. MEC [B102007-61194]
  2. AGAUR [2005SGR-00956]
  3. CIBER de Bioingenieria, Biornateriales y Nanomedicina (CIBER-BBN)

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The construction of non-viral. virus-like vehicles for gene therapy involves the functionalization of multipartite constructs with nucleic acid-binding, cationic agents. Short basic peptides, alone or as fusion proteins, are appropriate DNA binding and condensing elements, whose incorporation into gene delivery vehicles results in the formation of protein-DNA complexes of appropriate size for cell internalization and intracellular trafficking. We review here the most used cationic peptides for artificial virus construction as well as the recently implemented strategies to control the architecture and biological activities of the resulting nanosized particles. (c) 2009 Elsevier Inc. All rights reserved.

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