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Synthesis and Application of a Novel Ligand for Affinity Chromatography Based Removal of Endotoxin from Antibodies

机译:基于亲和色谱的抗体内毒素去除新配体的合成与应用

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Endotoxin or lipopolysaccharide (LPS) contamination in proteins expressed by Gram-negative bacteria is a major drawback associated with protein expression. Endotoxin intoxication in humans and animals above a certain threshold level can result in a fatal immune response. Reduction in endotoxin levels is therefore essential before proteins can be used in in vivo studies or sold as pharmaceutical products. Affinity chromatography employing the peptide Polymyxin B (PMB) as an affinity ligand is one way in which endotoxin contamination has been addressed; this is, however, a cosdy process. We describe the synthesis of a novel affinity ligand based on the structure of the drug pentamidine, which can be applied effectively in endotoxin removal. The synthetic route to this ligand is straightforward and inexpensive, while the ligand can be readily immobilized onto activated sepharose beads. Thus, we demonstrate that these pentamidine affinity beads bind endotoxin/LPS with comparable capacity to PMB affinity systems, that the beads can be recycled efficiently and economically without loss of binding capacity, and application of the functionalized beads for endotoxin removal in an authentic contaminated antibody sample.
机译:革兰氏阴性细菌表达的蛋白质中的内毒素或脂多糖(LPS)污染是与蛋白质表达相关的主要缺点。超过一定阈值水平的人类和动物内毒素中毒可导致致命的免疫反应。因此,在将蛋白用于体内研究或作为药物销售之前,降低内毒素水平至关重要。采用肽多粘菌素B(PMB)作为亲和配体的亲和色谱是解决内毒素污染的一种方法。但是,这是一个繁琐的过程。我们描述了基于药物喷他idine的结构的新型亲和配体的合成,可以有效地去除内毒素。合成该配体的途径是直接且廉价的,而该配体可以容易地固定在活化的琼脂糖珠上。因此,我们证明这些喷他tam亲和力珠粒结合内毒素/ LPS的能力与PMB亲和力系统相当,珠子可以有效且经济地回收而不会失去结合能力,并且可以应用功能化的珠粒来去除内毒素中的真实污染抗体样品。

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