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Refolding and purification of recombinant human VEGF-121 expressed as inclusion bodies in Escherichia coli / 南方医科大学学报
Journal of Southern Medical University ; (12): 1083-1086, 2006.
Article in English | WPRIM | ID: wpr-334990
ABSTRACT
Vascular endothelial growth factor 121 (VEGF(121)) was expressed as inclusion bodies by recombinant Escherichia coli. High concentrations of both biomass (46 g dry cell/L) and VEGF(121) inclusion bodies (4.5 g/L) were obtained by applying a high-cell-density culture. After the inclusion bodies were washed and dissolved, VEGF(121) was refolded at 0.2 mg/ml by ultrafiltration in refolding buffer with a yield of 81%. Renatured VEGF(121) was purified by anion chromatography and Sephacry S-100 chromatography with purity higher than 95% and final purification yield of 31%. The purified VEGF(121) could stimulate the proliferation of human umbilical vein endothelial cells as demonstrated by a biological activity assay.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Recombinant Proteins / Cell Line / Inclusion Bodies / Chemistry / Protein Folding / Cell Biology / Endothelial Cells / Vascular Endothelial Growth Factor A / Cell Proliferation Limits: Humans Language: English Journal: Journal of Southern Medical University Year: 2006 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pharmacology / Recombinant Proteins / Cell Line / Inclusion Bodies / Chemistry / Protein Folding / Cell Biology / Endothelial Cells / Vascular Endothelial Growth Factor A / Cell Proliferation Limits: Humans Language: English Journal: Journal of Southern Medical University Year: 2006 Type: Article