DNA微阵列
重组DNA
噬菌体展示
计算生物学
蛋白质组
蛋白质组学
蛋白质阵列分析
蛋白质微阵列
抗体
分子生物学
化学
生物
纳米技术
材料科学
生物化学
基因
基因表达
遗传学
作者
Cornelia Steinhauer,Christer Wingren,Ann‐Christin Malmborg Hager,Carl Borrebaeck
出处
期刊:BioTechniques
[Future Science Ltd]
日期:2002-12-01
卷期号:33 (sup6)
被引量:75
标识
DOI:10.2144/dec02steinhauer
摘要
High-throughput proteomics, based on the microarray platform, requires stable, highly functional components that will yield a highly sensitive read-out of low abundance proteins. Although antibodies are the best characterized binding molecules for this purpose, only a fraction of them appear to behave satisfactorily in the chip format. Therefore, high demands need to be placed on their molecular design. In the present study, we have focused on recombinant antibody design based on a single framework for protein chip applications, aiming at defining crucial molecular probe parameters. Our results show that engineered human recombinant scFv antibody fragments that displayed appropriate biophysical properties (molecular [functional] stability in particular) can be generated, making them prime candidates for high-density antibody arrays. In fact, a superior framework that displays both multifaceted adsorption properties and very high functional stability over several months on chips (stored in a dried-out state) was identified. Taken together, designed scFv fragments based on a single molecular scaffold, readily accessible in large phage display libraries, can undoubtedly meet the requirements of probe content in antibody microarrays, particularly for global proteome analysis.
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