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Purification of transgenic tobacco-derived recombinant human monoclonal antibody
被引:9
|作者:
Mayani, Mukesh
[1
]
Filipe, Carlos D. M.
[1
]
McLean, Michael D.
[2
]
Hall, J. Christopher
[2
]
Ghosh, Raja
[1
]
机构:
[1] McMaster Univ, Dept Chem Engn, Hamilton, ON L8S 4L7, Canada
[2] Univ Guelph, Dept Environm Biol, Guelph, ON N1G 2W1, Canada
基金:
加拿大自然科学与工程研究理事会;
关键词:
Monoclonal antibody;
Transgenic tobacco;
Purification;
Ultrafiltration;
Chromatography;
CASCADE ULTRAFILTRATION CONFIGURATION;
THERAPEUTIC PROTEINS;
BETA-GLUCURONIDASE;
PRECIPITATION;
EXPRESSION;
STRATEGY;
SYSTEM;
D O I:
10.1016/j.bej.2012.12.007
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:
Purification of recombinant monoclonal antibody from transgenic plant extract is technically challenging as it involves the processing of large volume of material, containing low titre of antibody, present along with large quantities of native proteins and other impurities. The conventional approach of capturing antibody from a clarified extract using packed-bed chromatography is therefore not particularly suitable. This study evaluates the suitability of using a combination of ultrafiltration and chromatography for purifying transgenic tobacco-derived human monoclonal antibody. A two-stage cascade ultrafiltration process removed about 97% impurities while ensuring almost complete recovery of antibody, providing 32-fold antibody enrichment in the process. The primary objective of the ultrafiltration step was to reduce the burden on the subsequent chromatographic steps. A two-step chromatographic process was then used to eliminate remaining impurities. Using this approach, recombinant human antibody expressed in tobacco could be purified to greater than 95% purity with 50% overall recovery (ca. 12.5 mg antibody/kg tobacco tissues). (C) 2012 Elsevier B.V. All rights reserved.
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页码:33 / 41
页数:9
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