Ethanol precipitation for purification of recombinant antibodies

被引:45
作者
Tscheliessnig, Anne [1 ]
Satzer, Peter [1 ]
Hammerschmidt, Nikolaus [1 ,2 ]
Schulz, Henk [3 ]
Helk, Bernhard [3 ]
Jungbauer, Alois [1 ,2 ]
机构
[1] Univ Nat Resources & Life Sci, Dept Biotechnol, A-1190 Vienna, Austria
[2] Austrian Ctr Ind Biotechnol, A-1190 Vienna, Austria
[3] Novartis Pharma AG, CH-4002 Basel, Switzerland
基金
奥地利科学基金会;
关键词
CHO; Recombinant antibodies; Cold ethanol precipitation; Organic solvent; Monolith; PLASMA-PROTEIN FRACTIONATION; MONOCLONAL-ANTIBODIES; IMMUNOGLOBULIN-G; PRION PROTEIN; CHROMATOGRAPHY; BIOPHARMACEUTICALS; PLATFORM; DESIGN; SYSTEM;
D O I
10.1016/j.jbiotec.2014.07.436
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
Currently, the golden standard for the purification of recombinant humanized antibodies (rhAbs) from CHO cell culture is protein A chromatography. However, due to increasing rhAbs titers alternative methods have come into focus. A new strategy for purification of recombinant human antibodies from CHO cell culture supernatant based on cold ethanol precipitation (CEP) and CaCl2 precipitation has been developed. This method is based on the cold ethanol precipitation, the process used for purification of antibodies and other components from blood plasma. We proof the applicability of the developed process for four different antibodies resulting in similar yield and purity as a protein A chromatography based process. This process can be further improved using an anion-exchange chromatography in flowthrough mode e.g. a monolith as last step so that residual host cell protein is reduced to a minimum. Beside the ethanolbased process, our data also suggest that ethanol could be replaced with methanol or isopropanol. The process is suited for continuous operation. (C) 2014 The Authors. Published by Elsevier B.V.
引用
收藏
页码:17 / 28
页数:12
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