Previous Article | Next Article ![]()
Journal of Virology, February 2001, p. 1571-1575, Vol. 75, No. 3
Committee on Virology1
and Department of Microbiology and Molecular
Genetics,2 Harvard Medical School, and
Howard Hughes Medical Institute at The Children's
Hospital,3 Boston, Massachusetts 02115, and
Department of Oncology, McArdle Laboratory for Cancer Research,
University of Wisconsin
Received 31 July 2000/Accepted 8 November 2000
Previously, we have demonstrated that bridge proteins comprised of
avian leukosis virus (ALV) receptors fused to epidermal growth factor
(EGF) can be used to selectively target retroviral vectors with ALV
envelope proteins to cells expressing EGF receptors. To determine
whether another type of ligand incorporated into an ALV
receptor-containing bridge protein can also function to target
retroviral infection, the TVA-VEGF110 bridge protein was generated.
TVA-VEGF110 consists of the extracellular domain of the TVA receptor
for ALV subgroup A (ALV-A), fused via a proline-rich linker peptide to
a 110-amino-acid form of vascular endothelial growth factor (VEGF).
This bridge protein bound specifically to its cell surface receptor,
VEGFR-2, and efficiently mediated the entry of an ALV-A vector into
cells. These studies indicate that ALV receptor-ligand bridge proteins
may be generally useful tools for retroviral targeting approaches.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.3.1571-1575.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Targeting Avian Leukosis Virus Subgroup A Vectors
by Using a TVA-VEGF Bridge Protein
Madison, Madison, Wisconsin
537064
*
Corresponding author. Mailing address: McArdle
Laboratory for Cancer Research, University of Wisconsin at Madison,
1400 University Ave., Madison, WI 53706. Phone: (608) 265-5151. Fax:
(608) 262-2824. E-mail: young{at}oncology.wisc.edu.
This article has been cited by other articles:
| J. Bacteriol. | Mol. Cell. Biol. | Microbiol. Mol. Biol. Rev. |
|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|