Paemanee Atchara, Wikan Nitwara, Roytrakul Sittiruk, Smith Duncan R
Institute of Molecular Biosciences, Mahidol University, Salaya Campus, 25/25 Phuttamontol Sai 4, Salaya, Nakorn Pathom, Thailand.
National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency, Pathum Thani, Thailand.
Methods Mol Biol. 2016;1426:179-93. doi: 10.1007/978-1-4939-3618-2_16.
Gel-enhanced liquid chromatography coupled with tandem mass spectrometry (GeLC-MS/MS) is a labor intensive, but relatively straightforward methodology that generates high proteome coverage which can be applied to the proteome analysis of a range of starting materials such as cells or patient specimens. Sample proteins are resolved electrophoretically in one dimension through a sodium dodecyl sulfate (SDS) polyacrylamide gel after which the lanes are sliced into sections. The sections are further diced and the gel cubes generated are subjected to in-gel tryptic digestion. The resultant peptides can then be analyzed by tandem mass spectroscopy to identify the proteins by database searching. The methodology can routinely detect several thousand proteins in one analysis. The protocol we describe here has been used with both cells in culture that have been infected with chikungunya virus and specimens from Chikungunya fever patients. This protocol details the process for generating peptides for subsequent mass spectroscopic and bioinformatic analysis.
凝胶增强液相色谱-串联质谱联用(GeLC-MS/MS)是一种劳动强度大但相对简单的方法,可实现高蛋白质组覆盖率,适用于对多种起始材料(如细胞或患者标本)进行蛋白质组分析。样品蛋白质先通过十二烷基硫酸钠(SDS)聚丙烯酰胺凝胶进行一维电泳分离,然后将泳道切成条带。这些条带进一步切碎,所得凝胶块进行胶内胰蛋白酶消化。然后,可通过串联质谱分析所得肽段,通过数据库搜索鉴定蛋白质。该方法通常一次分析就能检测到数千种蛋白质。我们在此描述的方案已用于感染基孔肯雅病毒的培养细胞和基孔肯雅热患者的标本。该方案详细说明了生成肽段以供后续质谱和生物信息学分析的过程。