Weak partitioning chromatography for anion exchange purification of monoclonal antibodies

被引:91
|
作者
Kelley, Brian D. [1 ]
Tobler, Scott A. [1 ]
Brown, Paul [1 ]
Coffman, Jonathan L. [1 ]
Godavarti, Ranga [1 ]
Iskra, Timothy [1 ]
Switzer, Mary [1 ]
Vunnum, Suresh [1 ]
机构
[1] Wyeth BloPharma, Purificat Proc Dev, Andover, MA 01810 USA
关键词
weak partitioning chromatography; anion exchange chromatography; monoclonal antibodies; protein purification;
D O I
10.1002/bit.21923
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Weak Partitioning chromatography (WPC) is an isocratic chromatographic protein separation method performed under mobile phase conditions where a significant amount of the product protein binds to the resin, well in excess of typical flowthrough operations. The more stringent load and wash conditions lead to improved removal of more tightly binding impurities, although at the cost of a reduction in step yield. The step yield can be restored by extending the column load and incorporating a short wash at the end of the load stage. The use of WPC with anion exchange resins enables a two-column cGMP purification platform to be used for many different mAbs. The operating window for WPC can be easily established using high throughput batch-binding screens. Under conditions that favor very strong product binding, competitive effects from product binding can give rise to a reduction in column loading capacity. Robust performance of WPC anion exchange chromatography has been demonstrated in multiple cGMP mAb purification processes. Excellent clearance of host cell proteins, leached Protein A, DNA, high molecular weight species, and model virus has been achieved.
引用
收藏
页码:553 / 566
页数:14
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