Producing recombinant adenovirus encoding green fluorescent protein (Ad-GFP) by suspension cultured HEK-293 N3S cells.
- Author:
Bo TIAN
1
;
Bin WU
;
Qun-Wei ZHANG
;
Jian-Jin BI
;
Lan WANG
;
Bao-Zhen ZHU
;
Yue GENG
;
Zu-Ze WU
Author Information
1. Academy of Life Science, Shandong Normal University, Jinan 250014, China.
- Publication Type:Journal Article
- MeSH:
Adenoviridae;
genetics;
growth & development;
isolation & purification;
Bioreactors;
microbiology;
Cell Line;
Gene Transfer Techniques;
Genetic Vectors;
Green Fluorescent Proteins;
genetics;
Humans;
Kidney;
cytology;
virology;
Recombinant Proteins;
biosynthesis;
genetics;
Recombination, Genetic;
Virus Cultivation;
instrumentation;
methods
- From:
Chinese Journal of Biotechnology
2007;23(5):915-918
- CountryChina
- Language:Chinese
-
Abstract:
Adenovirus vectors are one of the most promising gene transfer systems. They are of great value for gene therapy because these vectors achieve temporal high-level transgene expression and high gene transfer efficiency. To meet increasing needs of adenovirus vectors for gene therapy programs, parallel development of efficient, scalable and reproducible production processes is required. Perfusion cultivation of 293 cells is one of the most commonly used methods to produce adenovirus vectors and it is suitable for industrialized production specially. Experimental studies had been carried out to produce recombinant adenovirus containing the green fluorescent protein gene (Ad-GFP) by perfusion cultivation of HEK-293 N3S cells in a 5L stirring bioreactors. Perfusion rate was 1-2 volume/day. To infect the 293 N3S cells with Ad-GFP at the density of (2-4) x 10(6) cells/ ml. The time of collecting cells was 48 hours post infection. After three rounds of freeze/thaw and centrifugation, the crude viral lysates were stored at--80 degrees C until use. Then to get the Ad-GFP products by 2 x CsCl-gradient purification. The purity of the products was determined by the A260/A280 ratio and a high performance liquid chromatography (HPLC) assay. The infective titer was determined by a TCID50 assay. The culture term was 10-12 days. The infectious titer, the number of virus particle and the ratio of infectious titer to virus particle for the product were 1.0 x 10(11) IU/mL, 1.68 x 10(12) VP/mL and 6.0% IU/VP respectively. The A260/A280 ratio was 1.33, and the purity determined by HPLC was 99.2%. The cell specific productivity was around 1000 IU/cell. By perfusion cultivation of 293 N3S cells in a 5L stirring bioreactors, we established the production process for Ad-GFP, which paves a way to produce other recombinant adenovirus for gene therapy.
