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植物蛋白质微阵列的生成及抗原-抗体相互作用的研究。

Generation of plant protein microarrays and investigation of antigen-antibody interactions.

作者信息

Kersten Birgit, Feilner Tanja

机构信息

RZPD German Resource Center for Genome Research GmbH, Berlin.

出版信息

Methods Mol Biol. 2007;355:365-78. doi: 10.1385/1-59745-227-0:365.

Abstract

The application of proteomics methods, such as the protein microarray technology, in plant science has been strongly supported by the completion of genome sequencing projects of Arabidopsis thaliana and rice. In this chapter we describe a method to generate plant protein microarrays and to use them for characterizing monoclonal antibodies or polyclonal sera with regard to their specificity and cross-reactivity. The method starts with characterized E. coli cDNA expression clones encoding His-tagged plant proteins. After expression and purification of these recombinant proteins in high throughput, protein microarrays are generated utilizing a contact printer. For the detection of the recombinant proteins on the microarrays, an anti-RGS-His6 antibody is used. To characterize specific antibodies, the microarrays are incubated with the respective antibody solutions followed by fluorescently labeled secondary antibodies. Signal detection is performed by means of an arrayscanner system. Protein microarrays containing the whole proteome of a plant will represent the ideal format to test antibody specificity and cross-reactivity in the future.

摘要

拟南芥和水稻基因组测序项目的完成,有力地支持了蛋白质组学方法(如蛋白质微阵列技术)在植物科学中的应用。在本章中,我们描述了一种生成植物蛋白质微阵列的方法,并使用它们来表征单克隆抗体或多克隆血清的特异性和交叉反应性。该方法始于编码带His标签植物蛋白的经鉴定的大肠杆菌cDNA表达克隆。在高通量表达和纯化这些重组蛋白后,利用接触式打印机生成蛋白质微阵列。为了检测微阵列上的重组蛋白,使用抗RGS-His6抗体。为了表征特异性抗体,将微阵列与相应的抗体溶液孵育,然后用荧光标记的二抗进行检测。通过阵列扫描仪系统进行信号检测。包含植物全蛋白质组的蛋白质微阵列将成为未来测试抗体特异性和交叉反应性的理想形式。

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