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用于血清蛋白谱分析的重组抗体微阵列设计:补体蛋白的靶向研究

Design of recombinant antibody microarrays for serum protein profiling: targeting of complement proteins.

作者信息

Ingvarsson Johan, Larsson Anette, Sjöholm Anders G, Truedsson Lennart, Jansson Bo, Borrebaeck Carl A K, Wingren Christer

机构信息

Department of Immunotechnology, BMC D13, Lund University, SE-221 84 Lund, Sweden.

出版信息

J Proteome Res. 2007 Sep;6(9):3527-36. doi: 10.1021/pr070204f. Epub 2007 Aug 16.

Abstract

Antibody-based microarrays is a novel technology with great promise for high-throughput proteomics. The process of designing high-performing arrays has, however, turned out to be challenging. Here, we have designed the next generation of a human recombinant scFv antibody microarray platform for protein expression profiling of nonfractionated biotinylated human plasma and serum proteomes. The setup, based on black polymer Maxisorb slides interfaced with a fluorescent-based read-out system, was found to provide specific, sensitive (subpicomolar (pM) range) and reproducible means for protein profiling. Further, a chip-to-chip normalization protocol critical for comparing data generated on different chips was devised. Finally, the microarray data were found to correlate well with clinical laboratory data obtained using conventional methods, as demonstrated for a set of medium abundant (micromolar (microM) to nanomolar (nM) range) protein analytes in serum and plasma samples derived from healthy and complement-deficient individuals.

摘要

基于抗体的微阵列是一种在高通量蛋白质组学方面极具潜力的新技术。然而,设计高性能阵列的过程已证明具有挑战性。在此,我们设计了下一代人重组单链抗体片段(scFv)抗体微阵列平台,用于未分级生物素化人血浆和血清蛋白质组的蛋白质表达谱分析。基于黑色聚合物Maxisorb载玻片并与基于荧光的读出系统相结合的设置,被发现可为蛋白质谱分析提供特异、灵敏(亚皮摩尔(pM)范围)且可重复的方法。此外,还设计了对于比较不同芯片上产生的数据至关重要的芯片间归一化方案。最后,正如对来自健康个体和补体缺陷个体的血清和血浆样本中一组中等丰度(微摩尔(μM)至纳摩尔(nM)范围)蛋白质分析物所证明的那样,微阵列数据被发现与使用传统方法获得的临床实验室数据具有良好的相关性。

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