Sitek B, Sipos B, Pfeiffer K, Grzendowski M, Poschmann G, Hawranke E, Köper K, Klöppel G, Meyer H E, Stühler K
Medizinisches Proteom-Center, Ruhr-Universität Bochum, ZKF 1.43, Universitätsstrasse 150, 44801, Bochum, Germany.
Anal Bioanal Chem. 2008 May;391(1):361-5. doi: 10.1007/s00216-008-2042-8. Epub 2008 Apr 1.
Large-gel two-dimensional gel electrophoresis (2-DE) is the method of choice for high-resolution proteome analysis of complex protein mixtures. Until now, however, the advantages of large 2-DE in combination with multiplexed fluorescence dye protein labelling has been complicated by the separate handling and analysis of the second-dimension gels. Therefore, we adapted the large 2-DE procedure allowing us to run "one-piece" large 2-DE gels (40 cm x 30 cm) in the second dimension for high resolution proteome analysis. Here, we show that in combination with fluorescence dye protein saturation labelling "one-piece" large 2-DE enables analysis of small amounts of sample (3 microg protein) for high-resolution proteome analysis.
大胶二维凝胶电泳(2-DE)是对复杂蛋白质混合物进行高分辨率蛋白质组分析的首选方法。然而,到目前为止,大尺寸二维凝胶电泳与多重荧光染料蛋白质标记相结合的优势因二维凝胶的单独处理和分析而变得复杂。因此,我们改进了大尺寸二维凝胶电泳程序,使我们能够在二维中运行“一体式”大尺寸二维凝胶(40 cm×30 cm)以进行高分辨率蛋白质组分析。在此,我们表明,结合荧光染料蛋白质饱和标记,“一体式”大尺寸二维凝胶能够对少量样品(3微克蛋白质)进行高分辨率蛋白质组分析。