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High-performance monolith affinity chromatography for fast quantitation of immunoglobulin G

机译:高效能整体亲和色谱法可快速定量免疫球蛋白G

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摘要

High-performance monolith affinity chromatography employing protein A resins has been introduced previously for the fast purification of IgG from different sources. Here we describe the design and evaluation of a fast and specific method for quantitation of lgG from purified samples as well as crude supernatant from Chinese hamster ovary (CHO) cells. We used a commercially available affinity monolith with protein A as affinity ligand (CIM protein A HLD disk). Interferences of CHO host cell proteins with the quantitation of IgG from CHO supernatant were eliminated by a careful choice of the equilibration buffer. With this method developed, it is possible to quantify IgG within 5 min in a concentration range of 23-250 μg/ml. The calibration range of the method could be extended from 4 to 1000 μg/ml by adjusting the injection volume.The method was successfully validated by measuring the low limit of detection and quantification, inter- and intra-day precision and selectivity.
机译:先前已经引入了使用蛋白A树脂的高效整体亲和色谱,用于从不同来源快速纯化IgG。在这里,我们描述了一种快速,特异性的方法的设计和评估,该方法用于定量定量纯化样品和中国仓鼠卵巢(CHO)细胞的上清液中的IgG。我们使用了市售的亲和整体,其中蛋白A为亲和配体(CIM蛋白A HLD盘)。通过仔细选择平衡缓冲液,可以消除CHO宿主细胞蛋白干扰CHO上清液中IgG定量的干扰。通过开发这种方法,可以在5分钟内以23-250μg/ ml的浓度对IgG进行定量。通过调节进样量可以将该方法的校正范围从4μg/ ml扩展到1000μg/ ml。通过测量检测和定量下限,日间和日内精度和选择性成功地验证了该方法。

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