Comparison of protein A affinity sorbents III. Life time study

被引:107
作者
Hahn, R [1 ]
Shimahara, K [1 ]
Steindl, F [1 ]
Jungbauer, A [1 ]
机构
[1] Univ Nat Resources & Appl Life Sci, Dept Biotechnol, A-1190 Vienna, Austria
关键词
staphylococcus protein a; antibody; immunoglobulin; leakage; host cell protein;
D O I
10.1016/j.chroma.2005.10.083
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Protein A affinity chromatography is a popular purification method for immunoglobulins applied at various scales, ranging from micro-tube up to 10001 column formal. Three novel high capacity protein A affinity chromatography media have been subjected to a lifetime study using 50 consecutive purification cycles of a cell culture supernatant (CCS) containing a monoclonal antibody. Chromatographic conditions followed protocols used in industrial antibody processing, including stripping and cleaning-in-place of the resins. For all three media, no significant loss of purification performance (measured by sodium dodecylsulfate polyacrylamide gel electrophoresis and analytical size-exclusion chromatography (SEC)) could be observed over 50 cycles. Eluate samples were analyzed for leaked protein A and host cell protein (HCP) content. MabSelect SuRe, the first protein A affinity medium compatible with alkaline regeneration conditions, exhibited the lowest leakage levels, in the range of 1-3 ppm. For the media MabSelect Xtra and ProSep-vA Ultra, leakage levels were in the range of 30-40 ppm. Host cell protein content of eluates from MabSelect Xtra and SuRe were between 300 and 700 ppm, whereas for ProSep-vA Ultra 3000-4000 ppm was achieved. (c) 2006 Elsevier B.V. All rights reserved.
引用
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页码:224 / 231
页数:8
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