Evaluating antibody monomer separation from associated aggregates using mixed-mode chromatography

被引:47
作者
Gao, Dong [1 ]
Wang, Li-Li [1 ]
Lin, Dong-Qiang [2 ]
Yao, Shan-Jing [2 ]
机构
[1] Northwest Univ, Inst Modern Separat Sci, Key Lab Synthet & Nat Funct Mol Chem, Shaanxi Key Lab Modern Separat Sci,Minist Educ, Xian 710068, Peoples R China
[2] Zhejiang Univ, Dept Chem & Biol Engn, State Key Lab Chem Engn, Hangzhou 310027, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Mixed-mode chromatography; Capto adhere; Aggregate removal; Antibody; HYDROPHOBIC INTERACTION CHROMATOGRAPHY; CHARGE-INDUCTION CHROMATOGRAPHY; PROTEIN MONOMER/AGGREGATE PURIFICATION; MEMBRANE CHROMATOGRAPHY; IMMUNOGLOBULIN-G; LIGAND; ADSORPTION; REMOVAL; EXCHANGE; IGG;
D O I
10.1016/j.chroma.2013.04.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aggregate level is a key factor when assessing quality attributes of antibody product, since the aggregation might impact the biological activity of biopharmaceutical. Effective separation methods are usually essential in manufacturing processes. In this study, three mixed-mode resins, i.e. Capto adhere and two home-made resins with benzylamine and butylamine as the functional ligands (named BA and AB), were used to investigate the separation performances of antibody aggregate removal processes. In addition, two traditional resins (Q Sepharose FF and Phenyl Sepharose 6 FF) were also investigated to explore the role of molecular interaction in the aggregate removal. The results indicated that the removal efficiency was highly dependent on the mass loading. With the sample load of 50 mg/ml resin both Capto adhere and BA resins can significantly reduce the aggregate level from 20.5% to 2.6% and 2.4%, respectively, while a relatively low degree of aggregate reduction was found with the traditional resins. The research indicates that both hydrophobic interaction and electrostatic interaction are critical for the aggregate removal and the cooperativity of different molecular interactions is important for the effective aggregates removal with mixed-mode resins. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:70 / 75
页数:6
相关论文
共 42 条
[1]   Changes in the secondary structure of adsorbed IgG and F(ab')(2) studied by FTIR spectroscopy [J].
Buijs, J ;
Norde, W ;
Lichtenbelt, JWT .
LANGMUIR, 1996, 12 (06) :1605-1613
[2]   Salt-independent adsorption chromatography: new broad-spectrum affinity methods for protein capture [J].
Burton, SC ;
Harding, DRK .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2001, 49 (1-3) :275-287
[3]   The distinctive separation attributes of mixed-mode resins and their application in monoclonal antibody downstream purification process [J].
Chen, Jie ;
Tetrault, Jen ;
Zhang, Yanyu ;
Wasserman, Andy ;
Conley, Greg ;
DiLeo, Mike ;
Haimes, Elliot ;
Nixon, Andrew E. ;
Ley, Arthur .
JOURNAL OF CHROMATOGRAPHY A, 2010, 1217 (02) :216-224
[4]   Protein aggregation and bioprocessing [J].
Cromwell, Mary E. M. ;
Hilario, Eric ;
Jacobson, Fred .
AAPS JOURNAL, 2006, 8 (03) :E572-E579
[5]   Influence of osmolarity and pH increase to achieve a reduction of monoclonal antibodies aggregates in a production process [J].
Franco, R ;
Daniela, G ;
Fabrizio, M ;
Ilaria, G ;
Detlev, H .
CYTOTECHNOLOGY, 1999, 29 (01) :11-25
[6]   Improved antibody aggregate removal by hydroxyapatite chromatography in the presence of polyethylene glycol [J].
Gagnon, Pete .
JOURNAL OF IMMUNOLOGICAL METHODS, 2008, 336 (02) :222-228
[7]   Monoclonal antibody purification with hydroxyapatite [J].
Gagnon, Pete .
NEW BIOTECHNOLOGY, 2009, 25 (05) :287-293
[8]   IgG Aggregate Removal by Charged-Hydrophobic Mixed Mode Chromatography [J].
Gagnon, Pete .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2009, 10 (04) :434-439
[9]   Preparation and adsoription behavior of a cellulose-based, mixed-mode adsorbent with a benzylamine ligand for expanded bed applications [J].
Gao, Dong ;
Yao, Shan-Jing ;
Lin, Dong-Qiang .
JOURNAL OF APPLIED POLYMER SCIENCE, 2008, 107 (01) :674-682
[10]   Protein adsorption kinetics of mixed-mode adsorbent with benzylamine as functional ligand [J].
Gao, Dong ;
Lin, Dong-Qiang ;
Yao, Shan-Jing .
CHEMICAL ENGINEERING SCIENCE, 2006, 61 (22) :7260-7268