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首页> 外文期刊>Biotechnology Progress >Production of functional hepatocyte growth factor (HGF) in insect cells infected with an HGF-Recombinant baculovirus in a serum-free medium
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Production of functional hepatocyte growth factor (HGF) in insect cells infected with an HGF-Recombinant baculovirus in a serum-free medium

机译:在无血清培养基中感染了HGF重组杆状病毒的昆虫细胞中产生功能性肝细胞生长因子(HGF)

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Three insect cell lines, SL-7B cells derived from Spodoptera litura, Sf9, and High Five (Hi-5) cells, were used for the production of pro-hepatocyte growth factor (pro-HGF). Cells were cultured and then infected with a recombinant HGF-containing baculovirus in a serum-free medium. In SL-7B cells, pro-HGF is synthesized and excreted from the cells and late in infection is converted to a heterodimeric form of HGF even when the cells are grown in serum free medium. Conversion of a single-chain form of HGF (pro-HGF) into an HGF heterodimer was unexpected, as pro-HGF is normally cleaved by a serum protease called HGF activator. The proliferation activity of heparin-affinity- purified HGF from serum-free culture supernatant of SL-7B cells is comparable to that obtained from HGF converted by serum proteases, suggesting that SL-7B cells produce a functionally analogous protease to correctly process pro-HGF. This work reports, for the first time, on the feasibility of properly processing pro-HGF to form functional HGF by proteases from invertebrate cells in serum-free media. Avoiding the supplementation of sera provides the advantages of a low production cost, zero contamination of infectious agents from sera, and simple downstream product purification. Experimental results further demonstrate that the conversion of pro- HGF by insect cells is cell-line-dependent, because proteases in Hi-5 or Sf9 cells could not process pro-HGF as efficiently and properly as those in SL-7B cells.
机译:三种昆虫细胞系,来自斜纹夜蛾的SL-7B细胞,Sf9和高五(Hi-5)细胞被用于产生肝细胞生长因子(pro-HGF)。培养细胞,然后在无血清培养基中用含有重组HGF的杆状病毒感染。在SL-7B细胞中,原HGF被合成并从细胞中排出,并且即使细胞在无血清培养基中生长,感染后期也会转化为HGF的异二聚体形式。 HGF(pro-HGF)的单链形式向HGF异二聚体的转化是出乎意料的,因为pro-HGF通常被称为HGF激活剂的血清蛋白酶裂解。肝素亲和纯化的HGF从SL-7B细胞的无血清培养上清液的增殖活性与从血清蛋白酶转化的HGF获得的增殖活性相当,这表明SL-7B细胞产生功能类似的蛋白酶以正确处理pro-HGF 。这项工作首次报道了在无血清培养基中通过无脊椎动物细胞的蛋白酶正确加工前HGF形成功能性HGF的可行性。避免补充血清提供了以下优点:生产成本低,来自血清的传染原零污染和简单的下游产物纯化。实验结果进一步证明,昆虫细胞对前HGF的转化是细胞系依赖性的,因为Hi-5或Sf9细胞中的蛋白酶不能像SL-7B细胞中那样高效,正确地处理pro-HGF。

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