Miniaturisation pour la Synthèse, l'Analyse & la Protéomique (MSAP), USR CNRS 3290, Université de Lille 1 Sciences et Technologies, 59655 Villeneuve d'Ascq Cedex, France.
Anal Chem. 2012 Jul 3;84(13):5589-95. doi: 10.1021/ac3004874. Epub 2012 Jun 20.
2D FT-ICR MS allows the correlation between precursor and fragment ions by modulating ion cyclotron radii for fragmentation modes with radius-dependent efficiency in the ICR cell without the need for prior ion isolation. This technique has been successfully applied to ion-molecule reactions, Collision-induced dissociation and infrared multiphoton dissociation. In this study, we used electron capture dissociation for 2D FT-ICR MS for the first time, and we recorded two-dimensional mass spectra of peptides and a mixture of glycopeptides that showed fragments that are characteristic of ECD for each of the precursor ions in the sample. We compare the sequence coverage obtained with 2D ECD FT-ICR MS with the sequence coverage obtained with ECD MS/MS and compare the sensitivities of both techniques. We demonstrate how 2D ECD FT-ICR MS can be implemented to identify peptides and glycopeptides for proteomics analysis.
2D FT-ICR MS 通过在 ICR 单元中调制离子回旋半径,允许前体离子和碎片离子之间的相关,而无需预先离子隔离,对于具有半径依赖性效率的碎裂模式。这项技术已成功应用于离子-分子反应、碰撞诱导解离和红外多光子解离。在这项研究中,我们首次将电子俘获解离用于 2D FT-ICR MS,并记录了肽和糖肽混合物的二维质谱,显示了样品中每个前体离子的 ECD 的特征片段。我们比较了 2D ECD FT-ICR MS 获得的序列覆盖率与 ECD MS/MS 获得的序列覆盖率,并比较了这两种技术的灵敏度。我们展示了如何实施 2D ECD FT-ICR MS 来鉴定蛋白质组学分析中的肽和糖肽。