首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >Fortification of a protein-free cell culture medium with plant peptones improves cultivation and productivity of an interferon-γ-producing cho cell line
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Fortification of a protein-free cell culture medium with plant peptones improves cultivation and productivity of an interferon-γ-producing cho cell line

机译:用植物蛋白强化无蛋白细胞培养基可提高产生干扰素γ的cho细胞系的培养和生产力

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A strong tendency is currently emerging to remove not only serum but also any product of animal origin from animal cell culture media during production of recombinant proteins. This should facilitate downstream processing and improve biosafety. One way consists in the fortification of protein-free nutritive media with plant protein hydrolysates. To investigate the effects of plant peptones on mammalian cell cultivation and productivity, CHO 320 cells, a clone of CHO K1 cells genetically modified to secrete human interferon-γ(IFN-γ), were first adapted to cultivation in suspension in a protein-free medium. Both cell growth and IFN-γ secretion were found to be equivalent to those reached in serum-containing medium. Eight plant peptones, selected on the basis of their content in free amino acids and oligopeptides, as well as molecular weight distribution of oligopeptides, were tested for their ability to improve culture parameters. These were improved in the presence of three peptones, all having an important fraction of oligopeptides ranging from 1 to 10 kDa and a small proportion of peptides higher than 10 kDa. These peptones do not seem to add significantly to the nutritive potential to basal protein-free nutritive medium. Nevertheless, supplementation of an oligopeptide-enriched wheat peptone improved cell growth by up to 30% and IFN-γ production by up to 60% in shake-flask experiments. These results suggest that the use of plant peptones with potential growth factor–like or antiapoptotic bioactivities could improve mammalian cell cultivation in protein-free media while increasing the product biosafety.
机译:目前正在形成一种强烈的趋势,即在重组蛋白的生产过程中不仅从动物细胞培养基中去除血清,而且从动物细胞培养基中去除任何动物来源的产品。这应有助于下游加工并提高生物安全性。一种方法是用植物蛋白水解物强化无蛋白营养培养基。为了研究植物蛋白one对哺乳动物细胞培养和生产力的影响,首先对CHO 320细胞(一种经过基因修饰以分泌人干扰素-γ(IFN-γ)的CHO K1细胞克隆)进行了悬浮培养,使其不含蛋白质。中。发现细胞生长和IFN-γ分泌均与在含血清的培养基中达到的相等。根据其在游离氨基酸和寡肽中的含量以及寡肽的分子量分布,选择了八种植物蛋白one改善培养参数的能力。在存在三个蛋白presence的情况下,这些蛋白得到了改善,所有蛋白having均具有重要的寡肽级分,范围为1至10 kDa,小部分的肽高于10 kDa。这些蛋白ept似乎并未显着增加不含基础蛋白的营养培养基的营养潜力。然而,在摇瓶实验中,补充富含寡肽的小麦蛋白ept可将细胞生长最多提高30%,将IFN-γ产生最多提高60%。这些结果表明,使用具有潜在生长因子样或抗凋亡生物活性的植物蛋白one可以改善哺乳动物细胞在无蛋白培养基中的培养,同时提高产品的生物安全性。

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