Martins-de-Souza Daniel, Menezes de Oliveira Bruno, dos Santos Farias Alessandro, Horiuchi Ricardo Shiniti Oka, Crepaldi Domingues Cleyton, de Paula Eneida, Marangoni Sérgio, Gattaz Wagner Farid, Dias-Neto Emmanuel, Camillo Novello José
Departamento de Bioquímica, Instituto de Biologia, Universidade Estadual de Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil.
Brief Funct Genomic Proteomic. 2007 Mar;6(1):70-5. doi: 10.1093/bfgp/elm009. Epub 2007 Jun 7.
Protein extraction is the most important step to reveal a proteome by Two-Dimensional Gel Electrophoresis. Usually, the urea/thiourea based standard protein extraction buffer (SB) is combined with detergents with the aim of achieving better resolution and solubilization of different classes of proteins. In order to produce better gels and achieve the greatest spot resolution of Human Brain Proteins, comparisons using 2-DE of extracted proteins from Human Brain Frontal Cortex with SB constituents (7M Urea, 2M Thiourea and 100mM DTT) were made, using different detergent compositions in the buffer. SB preparations in combination with CHAPS and ASB-14 as well as with ASB-16 (reported for the first time in 2-DE experiments) have been tested. Our results confirm that the most efficient solubilizing solution for 2-DE analysis of cytosolic and membrane Human Brain Proteins is SB combined with 4% CHAPS and 2% ASB-14.
蛋白质提取是通过二维凝胶电泳揭示蛋白质组的最重要步骤。通常,基于尿素/硫脲的标准蛋白质提取缓冲液(SB)与去污剂结合,目的是实现不同类别的蛋白质更好的分辨率和溶解性。为了制备更好的凝胶并实现人脑蛋白质的最大斑点分辨率,使用缓冲液中不同的去污剂组合物,对来自人脑额叶皮质的提取蛋白质与SB成分(7M尿素、2M硫脲和100mM二硫苏糖醇)进行二维电泳比较。已经测试了SB制剂与CHAPS和ASB - 14以及与ASB - 16(首次在二维电泳实验中报道)的组合。我们的结果证实,用于细胞质和膜人脑蛋白质二维电泳分析的最有效增溶溶液是SB与4% CHAPS和2% ASB - 14的组合。