Vaezzadeh Ali R, Simicevic Jovan, Chauvet Alexis, François Patrice, Zimmermann-Ivol Catherine G, Lescuyer Pierre, Deshusses Jacques P M, Hochstrasser Denis F
Biomedical Proteomics Research Group, Department of Structural Biology and Bioinformatics, Geneva University, 1 rue Michel Servet, 1211 Geneva, Switzerland.
Rapid Commun Mass Spectrom. 2008 Sep;22(17):2667-76. doi: 10.1002/rcm.3658.
Imaging Mass Spectrometry (IMS) has emerged as a powerful technique in the field of proteomics. The use of Immobilized pH Gradient-IsoElectric Focusing (IPG-IEF) is also a new trend, as the first dimension of separation, in shotgun proteomics. We report a combination of these two outstanding technologies. This approach is based on the separation of shotgun-produced peptides by IPG-IEF. The peptides are then transferred by capillarity to a capture membrane, which is then scanned by the mass spectrometer to generate MS images. This high-throughput methodology allows a preview of the sample to be obtained in a single day. We report the application of this new pipeline for differential comparison of the membrane proteome of two different strains of Staphylococcus aureus bacteria in a proof-of-principle experiment.
成像质谱(IMS)已成为蛋白质组学领域一种强大的技术。使用固定化pH梯度-等电聚焦(IPG-IEF)作为鸟枪法蛋白质组学中第一维分离方法也是一种新趋势。我们报告了这两种杰出技术的结合。这种方法基于通过IPG-IEF分离鸟枪法产生的肽段。然后通过毛细管作用将肽段转移到捕获膜上,接着用质谱仪对其进行扫描以生成质谱图像。这种高通量方法能够在一天内获得样品的预览图。在一项原理验证实验中,我们报告了这种新流程在两种不同金黄色葡萄球菌菌株膜蛋白质组差异比较中的应用。