79
Views
22
CrossRef citations to date
0
Altmetric
Research Article

Factors Controlling the Efficiency of Tat-mediated Plasmid DNA Transfer

, &
Pages 39-47 | Received 21 Nov 2003, Accepted 11 Feb 2004, Published online: 03 Oct 2008

References

  • Adami, R.C., Collard, W.T., Gupta, S.A., Kwok, K.Y., Bonadio, J. and Rice, K.G. (1998) “Stability of peptide-condensed plasmid DNA formulations”, J. Pharm. Sci. 87, 678–683.
  • Astriab-Fisher, A., Sergueev, D., Fisher, M., Shaw, B.R. and Juliano, R.L. (2002) “Conjugates of antisense oligonucleotides with the Tat and Antennapedia cell-penetrating peptides: effects on cellular uptake, binding to target sequences, and biologic actions”, Pharm. Res. 19, 744–754.
  • Collins, L., Sawyer, G.J., Zhang, X.H., Gustafsson, K. and Fabre, J.W. (2000) “In vitro investigation of factors important for the delivery of an integrin-targeted nonviral DNA vector in organ transplantation”, Transplantation 69, 1168–1176.
  • Console, S., Marty, C., Garcia-Echeverria, C., Schwendener, R. and Ballmer-Hofer, K. (2003) “Antennapedia and HIV TAT ‘protein transduction domains’ promote endocytosis of high Mr cargo upon binding to cell surface glycosaminoglycans”, J. Biol. Chem. 278, 35109–35114.
  • Cotton, M., La¨ngle-Rouault, F., Kirlappos, H., Wagner, E., Mechtler, Zenke, M., et al. (1990) “Transferrin—polycation-mediated intro- duction of DNA into human leukemic cells: stimulation by agents that affect the survival of transfected DNA or modulate transferrin receptor levels”, Proc. Natl Acad. Sci. USA 87, 4033–4037.
  • Derossi, D., Calvet, S., Trembleau, A., Brunissen, A., Chassaing, G. and Prochiantz, A. (1996) “Cell internalization of the third helix of the Antennapedia homeodomain is receptor-independent”, J. Biol. Chem. 271, 18188–18193.
  • Elliott, G. and O’Hare, P. (1997) “Intercellular trafficking and protein delivery by a herpesvirus structural protein”, Cell 88, 223–223.
  • Finkel, T. and Epstein, S.E. (1995) “Gene therapy for vascular disease”, FASEB J. 9, 843–851.
  • Fominaya, J., Gasset, M., Garcia, R., Roncal, F., Albar, J.P. and Bernad, (2000) “An optimised amphiphilic cationic peptide as an efficient non-viral gene delivery vector”, J. Gene Med. 2, 455–464.
  • Frankel, A.D. and Young, J.A. (1998) “HIV-1: fifteen proteins and RNA”, Annu. Rev. Biochem. 67, 1–25.
  • Hellgren, I., Drvota, V., Piepper, R., Enoksson, S., Blomberg, P., Islam, K.B. and Sylve´n, C. (2000) “High-efficient nonviral gene transfer. In vivo and in vitro study”, Cell Mol. Life Sci. 57, 1326–1333. Ignatovich, I.A., Dizhe, E.B., Pavlotskaya, A.V., Akifiev, B.N., Burov, S.V., Orlov, S.V. and Perevozchikov, A.P. (2003) “Complexes of plasmid DNA with basic domain (47-57) of the HIV-1 Tat protein are transferred to mammalian cells by endocytosis-mediated pathways”, J. Biol. Chem. 278, 42625–42636.
  • Isner, J.M. (2002) “Myocardial gene therapy”, Nature 415, 234–239.
  • Kichler, A., Zauner, W., Ogris, M. and Wagner, E. (1998) “Influence of the DNA complexation medium on the transfection efficiency of lipospermine/DNA particles”, Gene Ther. 5, 855–860.
  • Lindsay, M.A. (2002) “Peptide-mediated cell delivery: application in protein target validation”, Curr. Opin. Pharmacol. 2, 587–594.
  • Nabel, E.G. and Nabel, G.J. (1994) “Complex models for the study of gene function in cardiovascular bioloy”, Annu. Rev. Physiol. 56, 741–761.
  • Nakanishi, M., Eguchi, A., Akuta, T., Nagoshi, E., Fujita, S., Okabe, J., Senda, T. and Hasegawa, M. (2003) “Basic peptides as functional components of non-viral gene transfer vehicles”, Curr. Protein Pept. Sci. 4, 141–150.
  • Ogris, M., Steinlein, P., Kursa, M., Mechtler, K., Kircheis, R. and Wagner, E. (1998) “The size of DNA/transferrin-PEI complexes is an important factor for gene expression in cultured cells”, Gene Ther. 5, 1425–1433.
  • Park, Y.J., Liang, J.F., Ko, K.S., Kim, S.W. and Yang, V.C. (2003) “Low molecular weight protamine as an efficient and nontoxic gene carrier: in vitro study”, J. Gene Med. 5, 700–711.
  • Richard, J.P., Melikov, K., Vives, E., Ramos, C., Verbeure, B., Gait, M.J., et al. (2003) “Cell-penetrating peptides”, J. Biol. Chem. 278, 585–590.
  • Rudolph, C., Plank, C., Lausier, J., Schillinger, U., Muller, R.H. and Rosenecker, J. (2003) “Oligomers of the arginine-rich motif of the HIV-1 Tat protein are capable of transferring plasmid DNA into cells”, J. Biol. Chem. 278, 11411–11418.
  • Silhol, M., Tyagi, M., Giacca, M., Lebleu, B. and Vives, E. (2002) “Different mechanisms for cellular internalisation of the HIV-1 Tat- derived cell penetrating peptide and recombinant proteins fused to Tat”, Eur. J. Biochem. 269, 494–501.
  • Siprashvili, Z., Scholl, F.A., Oliver, S.F., Adams, A., Contag, C.H., Wender, P.A. and Khavari, P.A. (2003) “Gene transfer via reversible plasmid condensation with cysteine-flanked, internally spaced arginine-rich peptides”, Hum. Gene Ther. 14, 1225–1233.
  • Thoren, P.E., Persson, D., Isakson, P., Goksor, M., Onfelt, A. and Norden, (2003) “Uptake of analogs of penetratin, Tat (48-60) and oligoarginine in live cells”, Biochem. Biophys. Res. Commun. 307, 100–107.
  • Torchilin, V.P., Levchenko, T.S., Rammohan, R., Volodina, N., Papahadjopoulos-Sternberg, B. and D’Souza, G.G.M. (2003) “Cell transfection in vitro and in vivo with non-toxic TAT peptide-liposome-DNA complexes”, PNAS 100, 1972–1977.
  • Tung, C.H., Mueller, S. and Weissleder, R. (2002) “Novel branching membrane translocational peptide as gene delivery vector”, Bioorg. Med. Chem. 10, 3609–3614. Tyagi, M., Rusnati, M., Presta, M. and Giacca, M. (2001) “Internalization of HIV-1 tat requires cell surface heparan sulfate proteoglycans”, J. Biol. Chem. 276, 3254–3261.
  • Verma, I.M. and Somia, N. (1997) “Gene therapy—promises, problems and prospects”, Nature 389, 239–242.
  • Vives, E., Brodin, P. and Lebleu, B. (1997) “A truncated HIV-1 tat protein basic domain rapidly translocates through the plasma membrane and accumulates in the cell nucleus”, J. Biol. Chem. 272, 16010–16017.
  • White, R.E., Wade-Martins, R., Hart, S.L., Frampton, J., Huey, B., Desai-Mehta, A., Cerosaletti, K.M., Concannon, P. and James, M.R. (2003) “Functional delivery of large genomic DNA to human cells with a peptide-lipid vector”, J. Gene Med. 5, 883–892.
  • Wiethoff, C.M. and Middaugh, C.R. (2003) “Barriers to nonviral gene delivery”, J. Pharm. Sci. 92, 203–217.
  • Yla-Herttuala, S. and Alitalo, K. (2003) “Gene transfer as a tool to induce therapeutic vascular growth”, Nat. Med. 9, 694–701.
  • Zhang, X., Collins, L., Sawyer, G.J., Dong, X., Qiu, Y. and Fabre, J.W. (2001) “In vivo gene delivery via portal vein and bile duct to individual lobes of the rat liver using a polylysine-based non-viral DNA vector in combination with chloroquine”, Hum. Gene Ther. 12, 2179–2190.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.