Schröder Christoph, Alhamdani Mohamed S S, Fellenberg Kurt, Bauer Andrea, Jacob Anette, Hoheisel Jörg D
Functional Genome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Methods Mol Biol. 2011;785:203-21. doi: 10.1007/978-1-61779-286-1_14.
Antibody microarrays are a multiplexing technique for the analyses of hundreds of different analytes in parallel from small sample volumes of few microlitres only. With sensitivities in the picomolar to femtomolar range, they are gaining importance in proteomic analyses. These sensitivities can be obtained for complex protein samples without any pre-fractionation or signal amplification. Also, no expensive or elaborate protein depletion steps are needed. As with custom DNA-microarrays, the implementation of a dual-colour assay adds to assay robustness and reproducibility and was therefore a focus of our technical implementation. In order to perform antibody microarray experiments for large sets of samples and analytes in a robust manner, it was essential to optimise the experimental layout, the protein extraction, labelling and incubation as well as data processing steps. Here, we present our current protocol, which is used for the simultaneous analysis of the abundance of more than 800 proteins in plasma, urine, and tissue samples.
抗体微阵列是一种多重技术,可从仅几微升的小样本体积中并行分析数百种不同的分析物。其灵敏度在皮摩尔到飞摩尔范围内,在蛋白质组分析中越来越重要。对于复杂的蛋白质样品,无需任何预分级或信号放大即可获得这些灵敏度。此外,不需要昂贵或复杂的蛋白质去除步骤。与定制DNA微阵列一样,双色检测的实施增加了检测的稳健性和可重复性,因此是我们技术实施的重点。为了以稳健的方式对大量样品和分析物进行抗体微阵列实验,优化实验布局、蛋白质提取、标记和孵育以及数据处理步骤至关重要。在这里,我们展示了我们目前的方案,该方案用于同时分析血浆、尿液和组织样品中800多种蛋白质的丰度。