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PepFect14 Peptide Vector for Efficient Gene Delivery in Cell Cultures
Stockholm University, Faculty of Science, Department of Neurochemistry.
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2013 (English)In: Molecular Pharmaceutics, ISSN 1543-8384, Vol. 10, no 1, 199-210 p.Article in journal (Refereed) Published
Abstract [en]

The successful applicability of gene therapy approaches will heavily rely on the development of efficient and safe nonviral gene delivery vectors, for example, cell-penetrating peptides (CPPs). CPPs can condense oligonucleotides and plasmid DNA (pDNA) into nanoparticles, thus allowing the transfection of genetic material into cells. However, despite few promising attempts, CPP-mediated pDNA delivery has been relatively inefficient due to the unfavorable nanoparticle characteristics or the nanoparticle entrapment to endocytic compartments. In many cases, both of these drawbacks could be alleviated by modifying CPPs with a stearic acid residue, as demonstrated in the delivery of both the pDNA and the short oligonucleotides. In this study, PepFect14 (PF14) peptide, previously used for the transport of shorter oligonucleotides, is demonstrated to be suited also for the delivery of pDNA. It is shown that PF14 forms stable nanoparticles with pDNA with a negative surface charge and size of around 130-170 nm. These nanoparticles facilitate efficient gene delivery and expression in a variety of regular adherent cell lines and also in difficult-to-transfect primary cells. Uptake studies indicate that PF14/pDNA nanoparticles are utilizing class A scavenger receptors (SCARA) and caveolae-mediated endocytosis as the main route for cellular internalization. Conclusively, PF14 is an efficient nonviral vector for gene delivery.

Place, publisher, year, edition, pages
2013. Vol. 10, no 1, 199-210 p.
Keyword [en]
cell-penetrating peptide, nanoparticle, gene delivery, plasmid delivery, nonviral delivery, stearylation
National Category
Natural Sciences
Research subject
Neurochemistry with Molecular Neurobiology
URN: urn:nbn:se:su:diva-84944DOI: 10.1021/mp3003557ISI: 000313156100021PubMedID: 23186360OAI: diva2:582066
Swedish Research CouncilSwedish Cancer SocietyKnut and Alice Wallenberg Foundation
Available from: 2013-01-03 Created: 2013-01-03 Last updated: 2015-04-21Bibliographically approved

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Lehto, TõnisLangel, Ülo
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