Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (331K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (41)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Bettinger, T.
Right arrow Articles by Seymour, L. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bettinger, T.
Right arrow Articles by Seymour, L. W.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2001, Vol. 29, No. 18 3882-3891
© 2001 Oxford University Press

Peptide-mediated RNA delivery: a novel approach for enhanced transfection of primary and post-mitotic cells

Thierry Bettinger*, Robert C. Carlisle, Martin L. Read, Manfred Ogris and Leonard W. Seymour

CRC Institute for Cancer Studies, University of Birmingham, Birmingham B15 2TA, UK

Synthetic vectors were evaluated for their ability to mediate efficient mRNA transfection. Initial results indicated that lipoplexes, but not polyplexes based on polyethylenimine (PEI, 25 and 22 kDa), poly(L-lysine) (PLL, 54 kDa) or dendrimers, mediated efficient translation of mRNA in B16-F10 cells. Significant mRNA transfection was achieved by lipoplex delivery in quiescent (passage 0) human umbilical vein endothelial cells (HUVEC), and by passage 4, 10.7% of HUVEC were transfected compared to 0.84% with DNA. Lack of expression with PEI 25 kDa/mRNA or PLL 54 kDa/mRNA in a cell-free translation assay and following cytoplasmic injection into Rat1 cells indicated that these polyplexes were too stable to release mRNA. In contrast, polyplexes formed using smaller PEI 2 kDa and PLL 3.4 kDa gave 5-fold greater expression in B16-F10 cells compared to DOTAP, but were dependent on chloroquine for transfection activity. Endosomolytic activity was incorporated by conjugating PEI 2 kDa to melittin and resulting PEI 2 kDa–melittin/mRNA polyplexes mediated high transfection levels in HeLa cells (31.1 ± 4.1%) and HUVEC (58.5 ± 2.9%) in the absence of chloroquine, that was potentiated to 52.2 ± 2.7 and 71.6 ± 1.7%, respectively, in the presence of chloroquine. These results demonstrate that mRNA polyplexes based on peptide-modified low molecular weight polycations can possess versatile properties including endosomolysis that should enable efficient non-viral mRNA transfection of quiescent and post-mitotic cells.

* To whom correspondence should be addressed at present address: Bracco Research, Department of Formulation, 31 Route de la Galaise, CH-1228 Plan-les-Ouates, Geneva, Switzerland. Tel: +41 22 884 88 08; Fax: +41 22 884 88 85; Email: tbettinger{at}brg.bracco.com


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
R. Marty, C. N. N'soukpoe-Kossi, D. M. Charbonneau, L. Kreplak, and H.-A. Tajmir-Riahi
Structural characterization of cationic lipid-tRNA complexes
Nucleic Acids Res., June 26, 2009; (2009) gkp543v1.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Breunig, U. Lungwitz, R. Liebl, and A. Goepferich
Breaking up the correlation between efficacy and toxicity for nonviral gene delivery
PNAS, September 4, 2007; 104(36): 14454 - 14459.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
P. J. Farrow, L. B. Barrett, M. Stevenson, K. D. Fisher, J. Finn, R. Spice, M. A. Allan, M. Berry, A. Logan, L. W. Seymour, et al.
Cytoplasmic expression systems triggered by mRNA yield increased gene expression in post-mitotic neurons
Nucleic Acids Res., July 11, 2006; 34(11): e80 - e80.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
M. L. Read, S. Singh, Z. Ahmed, M. Stevenson, S. S. Briggs, D. Oupicky, L. B. Barrett, R. Spice, M. Kendall, M. Berry, et al.
A versatile reducible polycation-based system for efficient delivery of a broad range of nucleic acids
Nucleic Acids Res., May 24, 2005; 33(9): e86 - e86.
[Abstract] [Full Text] [PDF]


Home page
Journal of Bioactive and Compatible PolymersHome page
A. L. Parker and L. W. Seymour
Targeting of Polyelectrolyte RNA Complexes to Cell Surface Integrins as an Efficient Cytoplasmic Transfection Mechanism
Journal of Bioactive and Compatible Polymers, July 1, 2002; 17(4): 229 - 238.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.