A simple plasmid-based transient gene expression method using High Five cells

• Published in: Journal of biotechnology Vol. 216; pp. 67 - 75
• Main Authors: Shen, Xiao, Pitol, Ana K., Bachmann, Virginie, Hacker, David L., Baldi, Lucia, Wurm, Florian M.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 20.12.2015
• Subjects: Animals; Autographa californica; Baculovirus; Biotechnology; Cell Count; Cell Line; Density; DNA - metabolism; Expression vector; Gene Expression; High Five cells; Humans; Lepidoptera; Lepidoptera - cytology; Mathematical analysis; Mathematical models; Nuclear polyhedrosis virus; Plasmids - metabolism; Polyethyleneimine; Polyethyleneimine - chemistry; Promoter Regions, Genetic; Proteins; Recombinant; Reproducibility of Results; Suspension culture; Suspensions; Transfection - methods; Transgenes; Transient gene expression; Trichoplusia ni; Vectors (mathematics); RFU; Polyethyleneimine; TNFR-Fc; MT; hr5; AcMNPV; CHO; High Five cells; EGFP; Transient gene expression; Suspension culture; TGE; hCMV; ie1; PEI; GPCR; OpMNV; VLP; MCS; BEVS; ELISA; Expression vector
• ISSN: 0168-1656; 1873-4863
• DOI: 10.1016/j.jbiotec.2015.10.007

•Development of method for plasmid-based transient gene expression in High Five cells.•Optimization of transfection process.•Investigation of promoter/enhancer combinations for gene expression.•Volumetric yields of 150ug/mL of a secreted fusion protein within 4 days of transfection.•Reproducibility and scalability of the method demonstrated. The High Five (H5) cell line, derived from the lepidopteran Trichoplusia ni, is one of the major insect cell hosts for the production of recombinant proteins using the baculovirus expression vector system (BEVS). Here, we describe a simple polyethylenimine (PEI)-based transient gene expression (TGE) process for the rapid production of recombinant proteins from suspension-adapted H5 cells. The method was optimized using two model proteins, enhanced green fluorescent protein (EGFP) and human tumor necrosis factor receptor-Fc fusion protein (TNFR-Fc). After screening several promoter and enhancer combinations for high levels of TNFR:Fc production, an expression vector containing the Autographa californica multicapsid nucleopolyhedrovirus immediate early 1 (ie1) promoter and homologous region 5 (hr5) enhancer was selected. Cells were transfected at a density of 2×106 cells/mL by direct addition of DNA and PEI. Under optimized conditions, a 90% transfection efficiency (percentage of EGFP-positive cells) was obtained. In addition, we observed volumetric TNFR-Fc yields over 150μg/mL within 4 days of transfection. The method was found to be reproducible and scalable to 300mL. This plasmid-based transient transfection process is a simple and efficient alternative to the BEVS for recombinant protein production in H5 cells.