Combined polyethylene glycol and CaCl2 precipitation for the capture and purification of recombinant antibodies

被引:46
作者
Sommer, Ralf [1 ]
Satzer, Peter [1 ]
Tscheliessnig, Anne [1 ]
Schulz, Henk [2 ]
Helk, Bernhard [2 ]
Jungbauer, Alois [1 ,3 ]
机构
[1] Univ Nat Resources & Life Sci Vienna, Dept Biotechnol, A-1190 Vienna, Austria
[2] Novartis Pharma AG, CH-4002 Basel, Switzerland
[3] Austrian Ctr Ind Biotechnol, Vienna, Austria
关键词
Protein A; mAb; PEG; Polyethylene glycol; Precipitation; CHO; PROTEIN PRECIPITATION; MONOCLONAL-ANTIBODIES; CHROMATOGRAPHY; OPTIMIZATION; CELLS; FRACTIONATION; DESIGN; MODEL;
D O I
10.1016/j.procbio.2014.07.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A direct capture step was developed for the purification of recombinant antibodies from clarified culture supernatants. This method is a combination of CaCl2 and polyethylene glycol (PEG) precipitation. For separation of high molecular weight impurities, such as dsDNA and aggregates, CaCl2 precipitation was the method of choice, and PEG precipitation was used for monoclonal antibody (mAb) capturing to separate low molecular weight impurities, mainly host cell proteins (HCP). Precipitation tests were performed with five different CHO cell culture supernatants, and showed yields of at least 80-95%. Purity was determined by size exclusion chromatography, HCP ELISA, and two-dimensional differential in-gel electrophoresis (2D DIGE); the measured values from CaCl2/PEG precipitation were comparable to those from Protein A purification. These results suggest that this novel purification method could be used as the basis for a platform process to capture antibodies from a clarified culture supernatant. CaCl2/PEG precipitation provides enough selectivity and recovery to substantiate replacing the Staphylococcus Protein A affinity chromatography step of the antibody purification process. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2001 / 2009
页数:9
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