Biologics Technology Research Laboratories, Daiichi Sankyo Co., Ltd, Ohra-gun, Gunma, Japan.
Graduate School of Science and Technology, Gunma University, Kiryu-shi, Gunma, Japan.
Biotechnol Prog. 2020 May;36(3):e2955. doi: 10.1002/btpr.2955. Epub 2020 Jan 21.
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 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.
流穿模式下的阴离子交换(AEX)层析是一种广泛应用的纯化工艺,用于从单克隆抗体(mAb)中去除工艺/产品相关杂质和外源性/内源性病毒。AEX 层析的流动相 pH 值通常设定为每个 mAb 等电点(pI)的一半以下(即 pI-0.5)或更低,与低离子强度结合使用,这些条件通常对 mAb 的回收率和杂质的去除都很满意。然而,我们最近在这些标准层析条件下遇到了 mAb1 与 AEX 树脂的紧密结合。这种异常的吸附行为似乎是 mAb1 表面不对称电荷分布的影响。我们发现,如果流动相的 pH 值更低、离子强度更高,mAb1 就不会与 AEX 树脂结合,但这些条件不会允许有效去除病毒。我们预测,使用膜吸附剂可能会提供有效的 mAb1 纯化,因为支撑基质具有网络结构,不易与蛋白质表面的不对称电荷分布发生相互作用。我们在标准层析条件下测试了 Natriflo HD-Q AEX 膜吸附剂,发现 mAb1 流经膜吸附剂,从而成功地与鼠白血病病毒分离。这种 AEX 膜吸附剂有望在工艺开发中发挥作用,因为无论 mAb 的电荷分布如何,它们都可以在类似的标准层析条件下进行纯化。