Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2012 May-Jun;30(3):766-81.
doi: 10.1016/j.biotechadv.2012.01.009. Epub 2012 Jan 28.

Co-expression vs. co-infection using baculovirus expression vectors in insect cell culture: Benefits and drawbacks

Affiliations
Review

Co-expression vs. co-infection using baculovirus expression vectors in insect cell culture: Benefits and drawbacks

Stanislav Sokolenko et al. Biotechnol Adv. 2012 May-Jun.

Abstract

The baculovirus expression vector system (BEVS) is a versatile and powerful platform for protein expression in insect cells. With the ability to approach similar post-translational modifications as in mammalian cells, the BEVS offers a number of advantages including high levels of expression as well as an inherent safety during manufacture and of the final product. Many BEVS products include proteins and protein complexes that require expression from more than one gene. This review examines the expression strategies that have been used to this end and focuses on the distinguishing features between those that make use of single polycistronic baculovirus (co-expression) and those that use multiple monocistronic baculoviruses (co-infection). Three major areas in which researchers have been able to take advantage of co-expression/co-infection are addressed, including compound structure-function studies, insect cell functionality augmentation, and VLP production. The core of the review discusses the parameters of interest for co-infection and co-expression with time of infection (TOI) and multiplicity of infection (MOI) highlighted for the former and the choice of promoter for the latter. In addition, an overview of modeling approaches is presented, with a suggested trajectory for future exploration. The review concludes with an examination of the gaps that still remain in co-expression/co-infection knowledge and practice.

PubMed Disclaimer

References

    1. Ailor E., Betenbaugh M.J. Overexpression of a cytosolic chaperone to improve solubility and secretion of a recombinant IgG protein in insect cells. Biotechnol Bioeng. 1998;58:196–203. - PubMed
    1. Alessi D.R., Saito Y., Campbell D.G., Cohen P., Sithanandam G., Rapp U. Identification of the sites in MAP kinase kinase-1 phosphorylated by p74raf-1. EMBO J. 1994;13:1610–1619. - PMC - PubMed
    1. Aucoin M.G., Perrier M., Kamen A.A. Improving AAV vector yield in insect cells by modulating the temperature after infection. Biotechnol Bioeng. 2007;97:1501–1509. - PubMed
    1. Aucoin M.G., Mena J.A., Kamen A.A. Bioprocessing of baculovirus vectors: a review. Curr Gene Ther. 2010;10:174–186. - PubMed
    1. Aucoin M.G., Perrier M., Kamen A.A. Production of adeno-associated viral vectors in insect cells using triple infection: optimization of baculovirus concentration ratios. Biotechnol Bioeng. 2006;95:1081–1092. - PubMed

Publication types

Substances

LinkOut - more resources