小直径柱中蛋白质的扩展床层析。1 .缩小规模和验证。

S Ghose, H Chase
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引用次数: 24

摘要

在蛋白质吸附和纯化中,由于优化运行中涉及的大量耗材,在扩展床色谱中使用大柱可能会对方法寻找造成限制。缩小这一技术的规模将为证明其在非常小的床上的可行性提供实用和必要的第一步。比较了直径分别为5.0、1.0和0.5 cm的三种色谱柱在流线- sp上的床层膨胀、流体动力学和溶菌酶吸附突破的性能。这代表了5厘米柱的100倍的缩小系数,并且根据所选标准的性能变化来判断是否成功。床层表征和突破运行表明,尽管在较小的柱中颗粒尺寸与柱径比较高,但塞流行为良好。柱的效率被发现是敏感的垂直排列,使其成为一个重要的问题,在规模缩小。这些研究结果表明,小直径柱可以有效地用于模拟规模系统的行为,为方法侦察研究提供了有用的工具。
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Expanded bed chromatography of proteins in small diameter columns. I. Scale down and validation.

The use of large columns for expanded-bed chromatography in protein adsorption and purification can pose limitations in method scouting due to the high volumes of consumables involved in optimisation runs. Scaling down this technique would provide a practical and necessary first step for demonstrating its feasibility in very small beds. The performance of three columns of diameters 5.0, 1.0 and 0.5 cm were compared in terms of the bed expansion, hydrodynamics and breakthrough for lysozyme adsorption onto STREAMLINE-SP. This represented a scale-down factor of a 100-fold from the 5-cm column and the success was judged by the insignificant changes in performance based on the selected criteria. Bed characterisation and breakthrough runs indicated good plug flow behaviour, despite the high particle size to column diameter ratio in the smaller columns. The column efficiency was found to be sensitive to the vertical alignment, making it an important issue in scale down. The results of these investigations show that small diameter columns can be effectively used for mimicking the behaviour in scale up systems providing a useful tool for method scouting studies.

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