Optimization of chimeric HIV-1 virus-like particle production in a baculovirus-insect cell expression system

Pillay, S., Meyers, A., Williamson, A. L., & Rybicki, E. P. (2009) Optimization of chimeric HIV-1 virus-like particle production in a baculovirus-insect cell expression system. Biotechnology Progress, 25(4), pp. 1153-1160.

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Abstract

A baculovirus-insect cell expression system potentially provides the means to produce prophylactic HIV-1 virus-like particle (VLP) vaccines inexpensively and in large quantities. However, the system must be optimized to maximize yields and increase process efficiency. In this study, we optimized the production of two novel, chimeric HIV-1 VLP vaccine candidates (GagRT and GagTN) in insect cells. This was done by monitoring the effects of four specific factors on VLP expression: these were insect cell line, cell density, multiplicity of infection (MOI), and infection time. The use of western blots, Gag p24 ELISA, and four-factorial ANOVA allowed the determination of the most favorable conditions for chimeric VLP production, as well as which factors affected VLP expression most significantly. Both VLP vaccine candidates favored similar optimal conditions, demonstrating higher yields of VLPs when produced in the Trichoplusia ni Pro insect cell line, at a cell density of 1 × 106 cells/mL, and an infection time of 96 h post infection. It was found that cell density and infection time were major influencing factors, but that MOI did not affect VLP expression significantly. This work provides a potentially valuable guideline for HIV-1 protein vaccine optimization, as well as for general optimization of a baculovirus-based expression system to produce complex recombinant proteins. © 2009 American Institute of Chemical Engineers.

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ID Code: 54960
Item Type: Journal Article
Refereed: Yes
Additional Information: Cited By (since 1996): 11
Export Date: 12 November 2012
Source: Scopus
Keywords: Chimera, Gag, HIV, RT, Vaccine
DOI: 10.1002/btpr.187
Deposited On: 20 Nov 2012 02:46
Last Modified: 20 Nov 2012 02:57

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