Secretory Expression of Human Vascular Endothelial Growth Factor (VEGF165) in Kluyveromyces lactis and Characterization of Its Biological Activity

Vascular endothelial growth factor 165 (VEGF 165 ) is the best characterized member and most potent endothelial cell mitogenic factor belonging to the VEGF family. Because VEGF 165 is the major player in angiogenesis in vivo and has potential in therapeutic applications for accelerating wound repair...

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Veröffentlicht in:International journal of peptide research and therapeutics 2021-09, Vol.27 (3), p.1989-2001
Hauptverfasser: Kuduğ Ceylan, Hülya, Erden Tayhan, Seçil, Gökçe, İsa
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Sprache:eng
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Zusammenfassung:Vascular endothelial growth factor 165 (VEGF 165 ) is the best characterized member and most potent endothelial cell mitogenic factor belonging to the VEGF family. Because VEGF 165 is the major player in angiogenesis in vivo and has potential in therapeutic applications for accelerating wound repair, many expression systems have been developed to produce VEGF 165 . In this study, biological active recombinant human VEGF 165 (rhVEGF 165 ) was expressed for the first time in Kluyveromyces lactis GG799 cells. The gene encoding human VEGF 165 was cloned in K. lactis genome by homologous recombination. The VEGF 165 was secreted in culture medium at a level of 5.7 mg/L and expression was confirmed by SDS-PAGE and Western blotting. Downstream purification was performed using ammonium sulphate precipitation and affinity chromatography. The biological activity of rhVEGF 165 was tested by the proliferation assay on the human umbilical vein-derived endothelial cells (HUVEC) in a dose and time-dependent manner. The K. lactis -derived rhVEGF 165 exhibited proliferative activity with a half-maximal effective concentration of 3.0. Cell migration analysis was conducted to evaluate the in vitro wound healing effect of the produced rhVEGF 165 via a scratch assay. These findings indicate that K. lactis could be a suitable host for secreting bioactive human VEGF 165 for therapeutic use. Graphical Abstract
ISSN:1573-3149
1573-3904
DOI:10.1007/s10989-021-10227-7