Novel endosomolytic peptides for enhancing gene delivery in nanoparticles

Research output: Contribution to journalArticleScientificpeer-review

Researchers

  • Aqeel Ahmad
  • Sanjeev Ranjan
  • Weikai Zhang
  • Jing Zou
  • Ilmari Pyykkö
  • Paavo K J Kinnunen

Research units

  • University of Helsinki
  • Tampere University

Abstract

Trapping in the endosomes is currently believed to represent the main barrier for transfection. Peptides, which allow endosomal escape have been demonstrated to overcome this barrier, similarly to the entry of viruses. However, the design principles of such endosomolytic peptides remain unclear. We characterized three analogs derived from membrane disrupting antimicrobial peptides (AMP), viz. LL-37, melittin, and bombolitin V, with glutamic acid substituting for all basic residues. These analogs are pH-sensitive and cause negligible membrane permeabilization and insignificant cytotoxicity at pH 7.4. However, at pH 5.0, prevailing in endosomes, membrane binding and hemolysis of human erythrocytes become evident. We first condensed the emerald green fluorescent protein (emGFP) containing plasmid by protamine, yielding 115 nm diameter soluble nanoplexes. For coating of the nanoplex surface with a lipid bilayer we introduced a hydrophobic tether, stearyl-octa-arginine (SR8). The indicated peptides were dissolved in methanol and combined with lipid mixtures in chloroform, followed by drying at RT under a nitrogen flow. The dry residues were hydrated with nanoplexes in Hepes, pH 7.4 yielding after a 30 min incubation at RT,rather monodisperse nanoparticles having an average diameter of 150-300 nm, measured by DLS and cryo-TEM. Studies with cell cultures showed the above peptides to yield expression levels comparable to those obtained using Lipofectamine 2000. However, unlike the polydisperse aggregates formed upon mixing Lipofectamine 2000 and plasmid, the procedure described yields soluble, and reasonably monodisperse nanoparticles, which can be expected to be suitable for gene delivery in vivo, using intravenous injection.

Details

Original languageEnglish
Pages (from-to)544-553
Number of pages10
JournalBiochimica et Biophysica Acta - Biomembranes
Volume1848
Issue number2
Publication statusPublished - 2015
MoE publication typeA1 Journal article-refereed

    Research areas

  • Endosomal escape, Endosomolytic peptides, Gene delivery, Gene expression, Nanoparticles, Transfection

ID: 10272083