J Gen Virol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 84 (2003), 2023-2031; DOI 10.1099/vir.0.19225-0

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rahman, Md. M.
Right arrow Articles by Gopinathan, K. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rahman, Md. M.
Right arrow Articles by Gopinathan, K. P.
Agricola
Right arrow Articles by Rahman, Md. M.
Right arrow Articles by Gopinathan, K. P.
© 2003 Society for General Microbiology

Bombyx mori nucleopolyhedrovirus-based surface display system for recombinant proteins

Md. Masmudur Rahman and Karumathil P. Gopinathan

Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India

Correspondence
Karumathil Gopinathan
kpg{at}mcbl.iisc.ernet.in

We describe here the development of a ‘eukaryotic display system’ for heterologous proteins on the viral and host cell surfaces using Bombyx mori nucleopolyhedrovirus (BmNPV). The reporter gene gfp (green fluorescent protein) was fused to either the gp64 gene encoding the full-length BmNPV envelope protein GP64 or to its 5' region encoding only the N-terminal domain harbouring the signal sequence, and recombinant viruses expressing the corresponding fusion proteins under the strong viral polyhedrin promoter were generated. On infection of the host insect B. mori or the host-derived BmN cells with the full-length GP64–GFP virus, abundant expression of the recombinant protein and its display on the cell surface were achieved. The fusion protein was also a component of the budded virions. Thus, the BmNPV-based display system provides an alternative to the previously established Autographa californica multinucleocapsid nucleopolyhedrovirus display system. The recombinant virus expressing GFP has also been used in preliminary pathological investigations on virus infection in B. mori and provides a simple method for screening for antiviral agents.




This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
N. Velappan, H. E. Fisher, E. Pesavento, L. Chasteen, S. D'Angelo, C. Kiss, M. Longmire, P. Pavlik, and A. R. M. Bradbury
A comprehensive analysis of filamentous phage display vectors for cytoplasmic proteins: an analysis with different fluorescent proteins
Nucleic Acids Res., March 1, 2010; 38(4): e22 - e22.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
Z.-N. Yang, H.-J. Xu, S. M. Thiem, Y.-P. Xu, J.-Q. Ge, X.-D. Tang, C.-H. Tian, and C.-X. Zhang
Bombyx mori nucleopolyhedrovirus ORF9 is a gene involved in the budded virus production and infectivity
J. Gen. Virol., January 1, 2009; 90(1): 162 - 169.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2003 by the Society for General Microbiology.