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基于噬菌体展示技术的蛋白质组规模抗体筛选

Towards proteome scale antibody selections using phage display.

机构信息

Technische Universität Braunschweig, Institute of Biochemistry and Biotechnology, Braunschweig, Germany.

出版信息

N Biotechnol. 2010 May 31;27(2):118-28. doi: 10.1016/j.nbt.2009.10.007. Epub 2009 Oct 31.

Abstract

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.

摘要

通过噬菌体展示技术对大型通用基因文库进行淘选,从而产生针对 60 多种不同抗原的抗体。特别有趣的是对结构基因组学联盟(SGC)提供的 20 种不同 SH2 结构域的淘选比较。德国国家基因组研究网络(NGFN)的“抗体工厂”内开发的用于高通量抗体生成的简化方法被证明可最大限度地减少工作量,并为抗体提供可靠而强大的来源。对于 SH2 结构域,在连续两个系列的选择中,分析了 2668 个克隆,在 ELISA 中产生了 347 个初级阳性结果。其中一半的阳性结果进一步分析,针对所有抗原鉴定出了超过 90 种不同的 scFv 抗体。通过交叉反应 ELISA、Western blot 和蛋白质微阵列对选定抗体的验证表明,体外抗体选择流水线具有多功能性,可生成具有高度特异性的单克隆结合物,数量可达到蛋白质组规模,工作量和时间显著减少。

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