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用于蛋白A色谱的有效柱冲洗溶剂的筛选

Screening of effective column rinse solvent for Protein-A chromatography.

作者信息

Yumioka Ryosuke, Tsumoto Kouhei, Arakawa Tsutomu, Ejima Daisuke

机构信息

Applied Research Department, Amino Science Laboratories, Ajinomoto, Inc., 1-1 Suzuki-cho, Kawasaki 210-8681, Japan.

出版信息

Protein Expr Purif. 2010 Apr;70(2):218-23. doi: 10.1016/j.pep.2009.09.019. Epub 2009 Oct 6.

Abstract

Mildly acidic arginine solution is highly effective in elution of bound proteins from Protein-A columns. Although Protein-A is specific in antibody capture, it does bind other proteins, which must then be removed before elution by aqueous arginine solution. If they are not removed, a strong elution property of aqueous arginine solutions will elute the contaminating proteins along with antibodies. Here we have examined various salt solutions as a column rinse solvent. We screened various solvents for their effects on binding of purified antibodies to Protein-A, instead of their effectiveness to elute the bound contaminants. Those solvents that result in a slight flow-through of the antibodies during loading should be effective in eluting non-specifically bound proteins that have weaker affinity for Protein-A than antibodies: namely, if a particular solvent reduces antibody binding to Protein-A, it is expected to be effective in reducing binding of contaminants and hence eluting them. Such screening showed a few compounds, including arginine and sodium acetate, as potential column rinse agents. A combination of arginine and sodium acetate was tested for a few crude materials containing antibodies.

摘要

轻度酸性的精氨酸溶液在从蛋白A柱上洗脱结合蛋白方面非常有效。虽然蛋白A对抗体捕获具有特异性,但它确实会结合其他蛋白质,在通过精氨酸水溶液洗脱之前必须将这些蛋白质去除。如果不去除它们,精氨酸水溶液的强洗脱特性会将污染蛋白与抗体一起洗脱下来。在这里,我们研究了各种盐溶液作为柱冲洗溶剂。我们筛选了各种溶剂对纯化抗体与蛋白A结合的影响,而不是它们洗脱结合污染物的有效性。那些在加载过程中导致抗体略有漏过的溶剂应该能有效洗脱对蛋白A亲和力比抗体弱的非特异性结合蛋白:也就是说,如果一种特定溶剂减少了抗体与蛋白A的结合,预计它能有效减少污染物的结合并因此将它们洗脱下来。这种筛选显示了一些化合物,包括精氨酸和醋酸钠,作为潜在的柱冲洗剂。对几种含抗体的粗原料测试了精氨酸和醋酸钠的组合。

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