PRODUCTION OF MOUSE MONOCLONAL-ANTIBODIES USING A CONTINUOUS CELL-CULTURE FERMENTER AND PROTEIN-G AFFINITY-CHROMATOGRAPHY

被引:4
作者
ZAMBONI, A [1 ]
GIUNTINI, I [1 ]
GIANESELLO, D [1 ]
MADDALENA, F [1 ]
ROGNONI, F [1 ]
HERBST, D [1 ]
机构
[1] BYK GULDEN ITALIA,RES DEPT 1,I-20032 CORMANO,ITALY
关键词
AFFINITY CHROMATOGRAPHY; FERMENTER; MONOCLONAL ANTIBODIES; PERFUSION PROCESS; PROTEIN G; STIRRED BIOREACTORS;
D O I
10.1007/BF00754610
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
The production of anti-alpha-fetoprotein monoclonal antibodies for diagnostic use was carried out in a stirred tank fermenter equipped with a double membrane stirrer for bubble free aeration and continuous medium perfusion. A serum-free medium supplemented with 4 mM L-glutamine and 2.0 g/l glucose with a protein content of only 780 mu g/ml was used for the production process. The harvested antibodies were concentrated 50-fold using a tangential ultrafiltration system and were then purified in a one step purification process by protein G affinity chromatography. The purity of the final product (90%) was controlled by SDS-polyacrylamide gel electrophoresis, gel exclusion chromatography and isoelectric focussing. For further quality controls of the product the immunoglobulin subclass and the isoelectric point were determined and the specificity of the purified mAb was tested by RIA using I-125 labelled alpha-fetoprotein. 1.87 g of purified monoclonal antibodies were produced (90% purity) within 2 weeks. It was found that the use of this type of stirred tank fermenter combined with a one step purification process using protein G affinity chromatography represents a suitable method for the fast production of medium scale quantities (500 mg - 5 g) of monoclonal antibodies for diagnostic use.
引用
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页码:79 / 87
页数:9
相关论文
共 19 条
[1]  
BIRCH JR, 1982, J CHEM BIOTECHNOL, V33, P313
[2]  
BLASEY HD, 1990, THESIS U HANNOVER FR
[3]   MURINE MONOCLONAL ISOTYPE SWITCH VARIANTS - DETECTION WITH RAT MONOCLONAL-ANTIBODIES IN ELISA AND ISOLATION BY SEQUENTIAL SUBLINING [J].
BOOT, JHA ;
GEERTS, MEJ ;
DEGROOT, ER ;
AARDEN, LA .
JOURNAL OF IMMUNOLOGICAL METHODS, 1988, 106 (02) :195-202
[4]  
BUNTEMEYER H, 1987, MODERN APPROACHES AN, P411
[5]  
CHARD T, 1990, INTRO RADIOIMMUNOA 2, V6
[6]  
ESSER C, 1990, ANNU REV IMMUNOL, V8, P717, DOI 10.1146/annurev.iy.08.040190.003441
[7]   STRUCTURE OF THE IGG-BINDING REGIONS OF STREPTOCOCCAL PROTEIN-G [J].
GUSS, B ;
ELIASSON, M ;
OLSSON, A ;
UHLEN, M ;
FREJ, AK ;
JORNVALL, H ;
FLOCK, JI ;
LINDBERG, M .
EMBO JOURNAL, 1986, 5 (07) :1567-1575
[8]  
HENKESHOVEN J, 1985, ELECTROPHORESIS, V6, P103
[9]   CELL-CULTURE ON ARTIFICIAL CAPILLARIES - APPROACH TO TISSUE GROWTH IN-VITRO [J].
KNAZEK, RA ;
KOHLER, PO ;
GULLINO, PM ;
DEDRICK, RL .
SCIENCE, 1972, 178 (4056) :65-+
[10]  
KOHLER G, 1975, NATURE, V245, P495