Selective enrichment of monospecific polyclonal antibodies for antibody-based proteomics efforts

被引:47
作者
Agaton, C
Falk, R
Guthenberg, IH
Göstring, L
Uhlén, M
Hober, S
机构
[1] AlbaNova Univ Ctr, KTH, Royal Inst Technol, Dept Biotechnol, S-10691 Stockholm, Sweden
[2] Affibody AB, S-16102 Stockholm, Sweden
关键词
proteomics; immobilized metal-ion affinity chromatography; affinity chromatography; antibodies; protein epitope signature tags;
D O I
10.1016/j.chroma.2004.06.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high stringency protocol, suitable for systematic purification of polyclonal antibodies, is described. The procedure is designed to allow the generation of target protein-specific antibodies suitable for functional annotation of proteins. Antibodies were generated by immunization with recombinantly produced affinity-tagged target proteins. To obtain stringent recovery of the antibodies, a two-step affinity chromatography principle was devised to first deplete the affinity tag-specific antibodies followed by a second step for affinity capture of the target protein-specific antibodies. An analytical dot-blot array system was developed to analyze the cross-reactivity of the affinity-purified antibodies. The results suggest that the protocol can be used in a highly parallel and automated manner to generate mono-specific polyclonal antibodies for large-scale, antibody-based proteomics efforts, i.e. affinity proteomics. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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