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The prevention of an anomalous chromatographic behavior and the resulting successful removal of viruses from monoclonal antibody with an asymmetric charge distribution by using a membrane adsorber in highly efficient, anion-exchange chromatography in flow-through mode

机译:通过在高效的阴离子交换色谱中使用膜吸附器在流通模式下,通过在高效的阴离子交换色谱中使用不对称电荷分布,预防异常的色谱行为和从单克隆抗体的病毒成功去除病毒

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Anion exchange (AEX) chromatography in the flow-through mode is a widely employed purification process for removal of process/product-related impurities and exogenous/endogenous viruses from monoclonal antibodies (mAbs). The pH of the mobile phase for AEX chromatography is typically set at half a unit below the isoelectric point (pI) of each mAb (i.e., pI - 0.5) or lower and, in combination with a low ionic strength, these conditions are usually satisfactory for both the recovery of the mAb and removal of impurities. However, we have recently encountered a tight binding of mAb1 to AEX resins under these standard chromatographic conditions. This anomalous adsorption behavior appears to be an effect of the asymmetric charge distribution on the surface of the mAb1. We found that mAb1 did not bind to the AEX resins if the mobile phase has a much lower pH and higher ionic strength, but those conditions would not allow adequate virus removal. We predicted that the use of membrane adsorbers might provide effective mAb1 purification, since the supporting matrix has a network structure that is would be less susceptible to interactions with the asymmetric charge distribution on the protein surface. We tested the Natriflo HD-Q AEX membrane adsorber under standard chromatographic conditions and found that mAb1 flowed through the membrane adsorber, resulting in successful separation from murine leukemia virus. This AEX membrane adsorber is expected to be useful for process development because mAbs can be purified under similar standard chromatographic conditions regardless of their charge distributions.
机译:流通式中的阴离子交换(AEX)色谱法是广泛采用的,用于从单克隆抗体(MAB)中除去方法/产品相关的杂质和外源/内源性病毒。用于AEX色谱的流动相的pH通常设定在每个MAB(即,PI-0.5)或更低的等电点(PI)下方的半单元处,并且与低离子强度组合,这些条件通常是令人满意的用于恢复mAb和去除杂质。然而,我们最近在这些标准的色谱条件下遇到了MAB1至AEX树脂的紧密结合。这种异常的吸附行为似乎是MAB1表面上的不对称电荷分布的效果。我们发现,如果流动相具有更低的pH和更高的离子强度,则MAB1没有结合AEX树脂,但这些条件不会允许充分的病毒去除。我们预测膜吸附器的使用可以提供有效的MAB1纯化,因为支撑基质具有与蛋白质表面上的不对称电荷分布的相互作用的网络结构。我们在标准色谱条件下测试了Natriflo HD-Q Aex膜吸附器,发现MAB1流过膜吸附器,导致鼠白血病病毒成功分离。该AEX膜吸附器预计可用于工艺开发,因为无论其电荷分布如何,都可以在类似的标准色谱条件下纯化MAB。

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