Towards proteome scale antibody selections using phage display

被引:41
作者
Mersmann, Michael [1 ]
Meier, Doris [1 ]
Mersmann, Jana [1 ]
Helmsing, Saskia [1 ]
Nilsson, Peter [2 ]
Graslund, Susanne [3 ]
Colwill, Karen [4 ]
Hust, Michael [1 ]
Duebel, Stefan [1 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Biochem & Biotechnol, D-38106 Braunschweig, Germany
[2] KTH Royal Inst Technol, Sch Biotechnol, Albanova Univ Ctr, Dept Prote, SE-10691 Stockholm, Sweden
[3] Karolinska Inst, Struct Genom Consortium, Dept Med Biochem & Biophys, S-17177 Stockholm, Sweden
[4] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
基金
加拿大健康研究院; 英国惠康基金;
关键词
RECOMBINANT ANTIBODIES; HIGH AVIDITY; FRAGMENTS; AFFINITY; GENERATION; EXPRESSION; ANTIGEN; DIAGNOSIS; SURFACE; VECTOR;
D O I
10.1016/j.nbt.2009.10.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In vitro antibody generation by panning a large universal gene library with phage display was employed to generate antibodies to more than 60 different antigens. Of particular interest was a comparison of pannings on 20 different SH2 domains provided by the Structural Genomics Consortium (SGC). Streamlined methods for high throughput antibody generation developed within the 'Antibody Factory' of the German National Genome Research Network (NGFN) were demonstrated to minimise effort and provide a reliable and robust source for antibodies. For the SH2 domains, in two successive series of selections, 2668 clones were analysed, resulting in 347 primary hits in ELISA. Half of these hits were further analysed, and more than 90 different scFv antibodies to all antigens were identified. The validation of selected antibodies by cross-reactivity ELISA, western blot and on protein microarrays demonstrated the versatility of the in vitro antibody selection pipeline to generate a renewable resource of highly specific monoclonal binders in proteome scale numbers with substantially reduced effort and time.
引用
收藏
页码:118 / 128
页数:11
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