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首页> 外文期刊>Biotechnology Progress >Proteomic Understanding of Intracellular Responses of Recombinant Chinese Hamster Ovary Cells Adapted to Grow in Serum-Free Suspension Culture
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Proteomic Understanding of Intracellular Responses of Recombinant Chinese Hamster Ovary Cells Adapted to Grow in Serum-Free Suspension Culture

机译:蛋白质组学对无血清悬浮培养中适应生长的重组中国仓鼠卵巢细胞胞内反应的理解

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To understand the intracellular responses in recombinant Chinese hamster ovary (rCHO) cells adapted to grow in serum-free suspension culture, a proteomic approach was employed. After rCHO cells producing erythropoietin were adapted to grow in suspension culture with the two different serum-free media (SFM4CHO~(TM) and SF-L1), proteome analyses were carried out using 2-D PAGE and based on spot intensities, 58 high-intensity protein spots were selected. Of the 58 protein spots, which represented 34 different kinds of proteins, 55 were identified by MALDI-TOF-MS, and MS/MS. Compared with the results in serum-containing medium, six proteins, four de novo synthesis of nucleotides-related proteins (dihydrolipoamide S-acetytransferase, transaldolase, inosine-5'-monophosphate dehydrogenase 2, and lymphoid-restricted membrane protein) and two molecular chaperones (heat shock protein 70 kDa and 60 kDa [HSC70, HSP60]) were significantly increased in SFM4CHO~(TM). From the results of proteomic analysis, HSP60 and HSC70, which were increased in both SFM, were selected as candidate proteins for engineering and rCHO cell lines overexpressing these genes were constructed. Cells overexpressing HSP60 and/or HSC70 showed 10-15% enhanced cell concentration during serum-free adaptation and 15-33% reduction in adaptation time. Taken together, identification of differentially expressed proteins in rCHO cells by a proteomic study can provide insights into understanding the intracellular events and clues to find candidate genes for cell engineering for improved performance of rCHO cells during adaptation to serum-free suspension culture.
机译:为了了解适合在无血清悬浮培养中生长的重组中国仓鼠卵巢(rCHO)细胞的细胞内反应,采用了蛋白质组学方法。使产生促红细胞生成素的rCHO细胞在两种不同的无血清培养基(SFM4CHO〜(TM)和SF-L1)的悬浮培养中生长后,使用2-D PAGE并基于斑点强度进行了蛋白质组分析,58高选择强度高的蛋白质斑点。在代表34种不同蛋白质的58个蛋白质斑点中,通过MALDI-TOF-MS和MS / MS鉴定出55个。与含血清的培养基中的结果相比,有六个蛋白,四个从头开始合成核苷酸相关蛋白(二氢脂酰胺S-乙酰转移酶,反式醛缩酶,肌苷5'-单磷酸脱氢酶2和淋巴样限制性膜蛋白)和两个分子伴侣。在SFM4CHO〜(TM)中,热休克蛋白70kDa和60kDa [HSC70,HSP60]显着增加。从蛋白质组学分析的结果中,选择在两种SFM中均增加的HSP60和HSC70作为工程蛋白的候选蛋白,并构建了过表达这些基因的rCHO细胞系。在无血清适应过程中,过表达HSP60和/或HSC70的细胞显示细胞浓度提高了10-15%,适应时间减少了15-33%。两者合计,通过蛋白质组学研究鉴定rCHO细胞中差异表达的蛋白质可以提供洞察力,以了解细胞内事件和线索,以寻找用于细胞工程的候选基因,从而在适应无血清悬浮培养过程中改善rCHO细胞的性能。

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