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Coupling Capillary Zone Electrophoresis with Electron Transfer Dissociation and Activated Ion Electron Transfer Dissociation for Top-Down Proteomics

机译:自上而下的蛋白质组学与毛细管区带电泳与电子转移解离和活化的离子电子转移解离的耦合

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Top-down proteomics offers the potential for full protein characterization, but many challenges remain for this approach, including efficient protein separations and effective fragmentation of intact proteins. Capillary zone electrophoresis (CZE) has shown great potential for separation of intact proteins, especially for differentially modified proteoforms of the same gene product. To date, however, CZE has been used Only with collision-based fragmentation methods. Here we report the first implementation of electron transfer dissociation (ETD) With online CZE separations for top-down proteomics, analyzing a mixture of four standard proteins and a complex protein mixture from the Mycobacterium marinum bacterial secretome. Using a multipurpose dissociation cell on an Orbitrap Elite system, we demonstrate that CZE is fully compatible with ETD as well as higher energy collisional dissociation (HCD), and that the two complementary fragmentation methods can be used in tandem on the electrophoretic time scale for improved protein characterization. Furthermore, we show that activated ion electron transfer dissociation (AI-ETD), a recently introduced Method for enhanced ETD fragmentation, provides useful performance with CZE separations to greatly increase protein characterization. When combined with HCD, AI-ETD improved the protein sequence coverage by more than 200% for proteins from both standard and complex mixtures, highlighting the benefits electron-driven dissociation methods can add to CZE separations.
机译:自上而下的蛋白质组学提供了完整蛋白质表征的潜力,但是这种方法仍然面临许多挑战,包括有效的蛋白质分离和完整蛋白质的有效片段化。毛细管区带电泳(CZE)已显示出分离完整蛋白质的巨大潜力,尤其是同一基因产物的差异修饰蛋白形式。但是,迄今为止,CZE仅用于基于冲突的分段方法。在这里,我们报告了自上而下的蛋白质组学与在线CZE分离的电子传递解离(ETD)的首次实施,分析了四种标准蛋白质的混合物和海分枝杆菌细菌分泌组的复杂蛋白质混合物。在Orbitrap Elite系统上使用多用途解离单元,我们证明CZE与ETD以及高能碰撞解离(HCD)完全兼容,并且两种互补的裂解方法可以在电泳时标上串联使用以改善蛋白质表征。此外,我们表明,活化离子电子转移解离(AI-ETD)是一种最新引入的增强ETD片段化的方法,可通过CZE分离提供有用的性能,从而大大提高蛋白质的表征。当与HCD结合使用时,AI-ETD可将标准混合物和复杂混合物中蛋白质的蛋白质序列覆盖率提高200%以上,突出了电​​子驱动解离方法可为CZE分离带来的好处。

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