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首页> 外文期刊>Biotechnology Progress >HPCE monitoring of the N-glycosylation pattern and sialylation of murine erythropoietin produced by CHO cells in batch processes
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HPCE monitoring of the N-glycosylation pattern and sialylation of murine erythropoietin produced by CHO cells in batch processes

机译:HPCE监测CHO细胞在间歇过程中产生的鼠促红细胞生成素的N-糖基化模式和唾液酸化

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Using capillary electrophoresis coupled to laser-induced fluorescence (HPCE-LIF), it was possible to profile N-linked oligosaccharides from EPO, including species containing sialic acid, during the Course of batch cultures performed either in serum-free or serum-containing medium. Although an unusual high heterogeneity of the N-linked oligosaccharides was observed by both SDS-PAGE and HPCE analysis, the patterns of mEPO glycans after desialylation by mild acid hydrolysis were found to be quite constant over the course of the cultures either with or without serum supplementation. In contrast, when the protein was analyzed by HPCE without acidic desialylation, fingerprints of N-linked olig-osaccharides changed with time in serum-containing conditions. This phenomenon appeared to be mainly due to the desialylation of mEPO as a result of a sialidase activity released upon cell lysis. These results demonstrate that though a higher EPO titer was obtained in serum supplemented conditions sialylation of EPO was severely affected by the presence of serum in the culture medium.
机译:通过在无血清或含血清培养基中进行分批培养的过程中,使用毛细管电泳和激光诱导荧光(HPCE-LIF),可以分析来自EPO的N-连接寡糖,包括唾液酸类物质。尽管通过SDS-PAGE和HPCE分析均观察到N-连接寡糖异常高的异质性,但发现在有或没有血清的情况下,通过轻度酸水解进行脱唾液酸化后,mEPO聚糖的模式是相当恒定的补充。相反,当通过不带酸性脱唾液酸化作用的HPCE分析蛋白质时,N-连接寡糖的指纹图谱在含血清的条件下随时间变化。这种现象似乎主要是由于细胞裂解后释放的唾液酸酶活性导致mEPO脱唾液酸化。这些结果表明,尽管在补充血清的条件下获得了更高的EPO效价,但是培养基中血清的存在严重影响了EPO的唾液酸化。

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