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Development of a serum-free culture medium for the large scale production of recombinant protein from a Chinese hamster ovary cell line

机译:开发无血清培养基以从中国仓鼠卵巢细胞系大规模生产重组蛋白

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A serum-free medium, WCM5, has been developed for the large scale propagation of CHO (Chinese hamster ovary) cells which express recombinant protein using dihydrofolate reductase as a selectable marker. WCM5 was prepared by supplementing Iscoves medium without lecithin, albumin or transferrin with a number of components which were shown to benefit growth. WCM5 medium contained 5 mg l?1 human recombinant insulin (Nucellin) but was otherwise protein-free. CHO 3D11* cells which had been engineered to express a humanised antibody, CAMPATH*-1H, were routinely grown using serum-containing medium. From a seeding density of 105 cells ml?1, cells grown in static culture with serum reached a maximal cell density of 6.5×105 cells ml?1 after 6 days in culture and produced a maximal antibody concentration of 69 mg l?1 after 11 days in culture. CHO 3D11* cells grown with serum were washed in serum-free medium then cultured in WCM5 medium. Following a period of adaptation the cell growth and product yield was superior to that achieved with serum-containing medium. CHO cells producing CAMPATH-1H grown in an 8000 l stirred bioreactor seeded with 2×105 cells ml?1 reached a maximal viable cell density of 2.16×106 cells ml?1 after 108 h in culture and a maximal antibody concentration of 131.1 mg l?1 after 122 h in culture.
机译:已经开发出一种无血清培养基WCM5,用于大规模繁殖CHO(中国仓鼠卵巢)细胞,该细胞使用二氢叶酸还原酶作为选择标记来表达重组蛋白。 WCM5是通过在不含卵磷脂,白蛋白或转铁蛋白的Iscoves培养基中添加许多已证明对生长有益的成分而制备的。 WCM5培养基含有5 mg l?1人重组胰岛素(Nucellin),但不含蛋白质。使用含有血清的培养基常规培养经过工程改造表达人源化抗体CAMPATH * -1H的CHO 3D11 *细胞。从105细胞ml?1的接种密度开始,在血清中静态培养的细胞在培养6天后达到6.5×105细胞ml?1的最大细胞密度,在11天后产生的最大抗体浓度为69 mg l?1文化的日子。将用血清培养的CHO 3D11 *细胞在无血清培养基中洗涤,然后在WCM5培养基中培养。适应一段时间后,细胞生长和产物产量要优于含血清的培养基。培养8000μl的生物反应器中生长的CAMPATH-1H CHO细胞在接种了2×105个细胞ml?1的细胞中培养108小时后,其最大活细胞密度为2.16×106个细胞ml?1,最大抗体浓度为131.1 mg l培养122小时后≥1。

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