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Overproduction of recombinant human VEGF (vascular endothelial growth factor) in Chinese hamster ovary cells
被引:0
|作者:
Lee, Seong-Baek
[2
,3
]
Park, Jeong Soo
[2
]
Lee, Seunghee
[2
]
Park, Junho
[2
]
Yu, Sungryul
[1
]
Kim, Heechan
[1
]
Kim, Dongjun
[2
]
Bytm, Tae Ho
[2
]
Baek, Kwanghee
[1
]
Ahn, Young-Joon
[3
]
Yoon, Jaeseung
[1
]
机构:
[1] Kyung Hee Univ, Grad Sch Biotechnol, Yongin 449701, South Korea
[2] PanGen Biotech Inc, Songnam 462807, South Korea
[3] Seoul Natl Univ, Sch Agr Biotechnol, Seoul 151921, South Korea
关键词:
VEGF;
Chinese hamster ovary (CHO) cell;
recombinant protein expression;
stable cell line;
bioreactor process;
D O I:
暂无
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Vascular endothelial growth factors (VEGFs) are a family of proteins that mediate angiogenesis. VEGF(165) is a VEGF-A isoform and has been extensively studied owing to its potential use in therapeutic angiogenesis. This study established Chinese hamster ovary (CHO) cells overexpressing recombinant human VEGF(165) (rhVEGF(165)) protein. The production rate of the established CHO cells was over 80 mg/l of rhVEGF(165) protein from a 7-day batch culture process using a 7.5-1 bioreactor with a 5-1 working volume and serum-free medium. The rhVEGF(165) protein was purified to homogeneity from the culture supernatant using a two-step chromatographic procedure that resulted in a 48%, recovery rate. The purified rhVEGF(165) protein was a glycosylated homodimeric protein with a higher molecular weight (MW) than the protein expressed from insect cells, suggesting that the glycosylation of the rhVEGF(165) protein in CHO cells differed from that in insect cells. The purified rhVEGF(165) protein in this study was functionally active with a half-maximal effective concentration of 3.8 ng/ml and specific activity of 2.5 x 10(5) U/mg.
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页码:183 / 187
页数:5
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