Abstract
Viral vectors displaying specific ligand binding moities such as scFv fragments or intact antibodies hold promise for the development of targeted gene therapy vectors. In this report we describe baculoviral vectors displaying either functional scFv fragments or the synthetic Z/ZZ IgG binding domain derived from protein A. Display on the baculovirus surface was achieved via fusion of the scFv fragment or Z/ZZ domain to the N-terminus of gp64, the major envelope protein of the Autographa californica nuclear polyhedrosis virus, AcNPV. As examples of scFv fragments we have used a murine scFv specific for the hapten 2-phenyloxazolone and a human scFv specific for carcinoembryonic antigen. In principle, the Z/ZZ IgG binding domain displaying baculoviruses could be targeted to specific cell types via the binding of an appropriate antibody. We envisage applications for scFv and Z/ZZ domain displaying baculoviral vectors in the gene therapy field.
Original language | English |
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Pages (from-to) | 84 - 90 |
Number of pages | 7 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 275 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2000 |
MoE publication type | A1 Journal article-refereed |
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Baculoviral display of functional scFv and synthetic IgG-binding domains. / Mottershead, David; Alfthan, Kaija; Ojala, Kirsi; Takkinen, Kristiina; Oker-Blom, Christian (Corresponding Author).
In: Biochemical and Biophysical Research Communications, Vol. 275, No. 1, 2000, p. 84 - 90.Research output: Contribution to journal › Article › Scientific › peer-review
TY - JOUR
T1 - Baculoviral display of functional scFv and synthetic IgG-binding domains
AU - Mottershead, David
AU - Alfthan, Kaija
AU - Ojala, Kirsi
AU - Takkinen, Kristiina
AU - Oker-Blom, Christian
PY - 2000
Y1 - 2000
N2 - Viral vectors displaying specific ligand binding moities such as scFv fragments or intact antibodies hold promise for the development of targeted gene therapy vectors. In this report we describe baculoviral vectors displaying either functional scFv fragments or the synthetic Z/ZZ IgG binding domain derived from protein A. Display on the baculovirus surface was achieved via fusion of the scFv fragment or Z/ZZ domain to the N-terminus of gp64, the major envelope protein of the Autographa californica nuclear polyhedrosis virus, AcNPV. As examples of scFv fragments we have used a murine scFv specific for the hapten 2-phenyloxazolone and a human scFv specific for carcinoembryonic antigen. In principle, the Z/ZZ IgG binding domain displaying baculoviruses could be targeted to specific cell types via the binding of an appropriate antibody. We envisage applications for scFv and Z/ZZ domain displaying baculoviral vectors in the gene therapy field.
AB - Viral vectors displaying specific ligand binding moities such as scFv fragments or intact antibodies hold promise for the development of targeted gene therapy vectors. In this report we describe baculoviral vectors displaying either functional scFv fragments or the synthetic Z/ZZ IgG binding domain derived from protein A. Display on the baculovirus surface was achieved via fusion of the scFv fragment or Z/ZZ domain to the N-terminus of gp64, the major envelope protein of the Autographa californica nuclear polyhedrosis virus, AcNPV. As examples of scFv fragments we have used a murine scFv specific for the hapten 2-phenyloxazolone and a human scFv specific for carcinoembryonic antigen. In principle, the Z/ZZ IgG binding domain displaying baculoviruses could be targeted to specific cell types via the binding of an appropriate antibody. We envisage applications for scFv and Z/ZZ domain displaying baculoviral vectors in the gene therapy field.
U2 - 10.1006/bbrc.2000.3264
DO - 10.1006/bbrc.2000.3264
M3 - Article
VL - 275
SP - 84
EP - 90
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
SN - 0006-291X
IS - 1
ER -