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A high-throughput microchip-based glycan screening assay for antibody cell culture samples

机译:基于高通量微芯片的抗体细胞培养样品聚糖筛选试验

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摘要

A high-throughput screening assay was developed to quantify major glycan species in the crude mammalian cell culture samples for monoclonal antibodies (mAbs). This method utilizes high-speed microchip electrophoresis separation following a fast sample preparation procedure. Using a 96-well ultra-filtration membrane, interfering species in the cell culture media were efficiently removed as the samples were concentrated. A commercial microchip electrophoresis instrument was used for high-speed separation, allowing each sample to be analyzed in less than 1 min. This method is well suited for the purpose of high-throughput antibody glycan profiling during cell culture expression, including clone selection and cell culture process optimization. The relative levels of high mannose (HM), fucosylated and galactosylated glycan species in the Fc domain can be determined for hundreds of crude cell culture samples in a few hours.
机译:开发了一种高通量筛选测定法,以对哺乳动物细胞粗品样本中的单克隆抗体(mAb)的主要聚糖种类进行定量。该方法利用快速的样品制备程序进行高速微芯片电泳分离。使用96孔超滤膜,可在样品浓缩时有效去除细胞培养基中的干扰物质。使用商用微芯片电泳仪进行高速分离,可以在不到1分钟的时间内对每个样品进行分析。此方法非常适合在细胞培养表达过程中进行高通量抗体聚糖分析的目的,包括克隆选择和细胞培养过程优化。可以在几个小时内确定数百个粗细胞培养样品中Fc域中高甘露糖(HM),岩藻糖基化和半乳糖基化的聚糖种类的相对水平。

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