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Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening

In addition to the expression of recombinant proteins, baculoviruses have been developed as a platform for the display of complex eukaryotic proteins on the surface of virus particles or infected insect cells. Surface display has been used extensively for antigen presentation and targeted gene deliv...

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Autores principales: Xu, Xiaodong, Chen, Yuanrong, Zhao, Yu, Liu, Xiaofen, Dong, Beitao, Jones, Ian M., Chen, Hongying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554712/
https://www.ncbi.nlm.nih.gov/pubmed/23365677
http://dx.doi.org/10.1371/journal.pone.0054631
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author Xu, Xiaodong
Chen, Yuanrong
Zhao, Yu
Liu, Xiaofen
Dong, Beitao
Jones, Ian M.
Chen, Hongying
author_facet Xu, Xiaodong
Chen, Yuanrong
Zhao, Yu
Liu, Xiaofen
Dong, Beitao
Jones, Ian M.
Chen, Hongying
author_sort Xu, Xiaodong
collection PubMed
description In addition to the expression of recombinant proteins, baculoviruses have been developed as a platform for the display of complex eukaryotic proteins on the surface of virus particles or infected insect cells. Surface display has been used extensively for antigen presentation and targeted gene delivery but is also a candidate for the display of protein libraries for molecular screening. However, although baculovirus gene libraries can be efficiently expressed and displayed on the surface of insect cells, target gene selection is inefficient probably due to super-infection which gives rise to cells expressing more than one protein. In this report baculovirus superinfection of Sf9 cells has been investigated by the use of two recombinant multiple nucleopolyhedrovirus carrying green or red fluorescent proteins under the control of both early and late promoters (vAcBacGFP and vAcBacDsRed). The reporter gene expression was detected 8 hours after the infection of vAcBacGFP and cells in early and late phases of infection could be distinguished by the fluorescence intensity of the expressed protein. Simultaneous infection with vAcBacGFP and vAcBacDsRed viruses each at 0.5 MOI resulted in 80% of infected cells co-expressing the two fluorescent proteins at 48 hours post infection (hpi), and subsequent infection with the two viruses resulted in similar co-infection rate. Most Sf9 cells were re-infectable within the first several hours post infection, but the re-infection rate then decreased to a very low level by 16 hpi. Our data demonstrate that Sf9 cells were easily super-infectable during baculovirus infection, and super-infection could occur simultaneously at the time of the primary infection or subsequently during secondary infection by progeny viruses. The efficiency of super-infection may explain the difficulties of baculovirus display library screening but would benefit the production of complex proteins requiring co-expression of multiple polypeptides.
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spelling pubmed-35547122013-01-30 Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening Xu, Xiaodong Chen, Yuanrong Zhao, Yu Liu, Xiaofen Dong, Beitao Jones, Ian M. Chen, Hongying PLoS One Research Article In addition to the expression of recombinant proteins, baculoviruses have been developed as a platform for the display of complex eukaryotic proteins on the surface of virus particles or infected insect cells. Surface display has been used extensively for antigen presentation and targeted gene delivery but is also a candidate for the display of protein libraries for molecular screening. However, although baculovirus gene libraries can be efficiently expressed and displayed on the surface of insect cells, target gene selection is inefficient probably due to super-infection which gives rise to cells expressing more than one protein. In this report baculovirus superinfection of Sf9 cells has been investigated by the use of two recombinant multiple nucleopolyhedrovirus carrying green or red fluorescent proteins under the control of both early and late promoters (vAcBacGFP and vAcBacDsRed). The reporter gene expression was detected 8 hours after the infection of vAcBacGFP and cells in early and late phases of infection could be distinguished by the fluorescence intensity of the expressed protein. Simultaneous infection with vAcBacGFP and vAcBacDsRed viruses each at 0.5 MOI resulted in 80% of infected cells co-expressing the two fluorescent proteins at 48 hours post infection (hpi), and subsequent infection with the two viruses resulted in similar co-infection rate. Most Sf9 cells were re-infectable within the first several hours post infection, but the re-infection rate then decreased to a very low level by 16 hpi. Our data demonstrate that Sf9 cells were easily super-infectable during baculovirus infection, and super-infection could occur simultaneously at the time of the primary infection or subsequently during secondary infection by progeny viruses. The efficiency of super-infection may explain the difficulties of baculovirus display library screening but would benefit the production of complex proteins requiring co-expression of multiple polypeptides. Public Library of Science 2013-01-24 /pmc/articles/PMC3554712/ /pubmed/23365677 http://dx.doi.org/10.1371/journal.pone.0054631 Text en © 2013 Xu et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Xu, Xiaodong
Chen, Yuanrong
Zhao, Yu
Liu, Xiaofen
Dong, Beitao
Jones, Ian M.
Chen, Hongying
Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening
title Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening
title_full Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening
title_fullStr Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening
title_full_unstemmed Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening
title_short Baculovirus Superinfection: A Probable Restriction Factor on the Surface Display of Proteins for Library Screening
title_sort baculovirus superinfection: a probable restriction factor on the surface display of proteins for library screening
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3554712/
https://www.ncbi.nlm.nih.gov/pubmed/23365677
http://dx.doi.org/10.1371/journal.pone.0054631
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