Optimizing expression and purification from cell culture medium of trispecific recombinant antibody derivatives

被引:22
作者
Willems, A [1 ]
Leoen, J [1 ]
Schoonooghe, S [1 ]
Grooten, J [1 ]
Mertens, N [1 ]
机构
[1] State Univ Ghent VIB, Dept Mol Biomed Res, B-9000 Ghent, Belgium
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2003年 / 786卷 / 1-2期
关键词
expression; purification; bispecific antibodies; Fab fragment; single-chain variable fragments;
D O I
10.1016/S1570-0232(02)00813-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibody fragments offer the possibility to build multifunctional manifolds tailored to meet a large variety of needs. We optimized the production of a manifold consisting of one(body) or two (tribody) single-chain variable fragments coupled to the C-terminus of Fab chains. Different strong mammalian promoters were compared and the influence of expression media on production and recovery was investigated. Since the physical and chemical nature of these molecules largely depends on the nature of the antibody building blocks incorporated, a generally applicable process for the purification of recombinant antibody derivatives from serum containing mammalian cell culture medium was designed. To this end we compared protein L, hydroxyapatite, immobilized metal affinity chromatography, cation-exchange chromatography and hydrophobic charge induction chromatography. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:161 / 176
页数:16
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