首页> 美国卫生研究院文献>Journal of Biomolecular Techniques : JBT >P144-T Top Down Sequence Analysis of Intact Protein Species Using a Novel Travelling Wave Ion Mobility Device Coupled With a Time-of-Flight Mass Spectrometer
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P144-T Top Down Sequence Analysis of Intact Protein Species Using a Novel Travelling Wave Ion Mobility Device Coupled With a Time-of-Flight Mass Spectrometer

机译:使用新型行波离子迁移仪和飞行时间质谱仪对完整蛋白物种进行P144-T自上而下的序列分析

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摘要

In this presentation we will demonstrate the utility of Ion Mobility Spectrometry in the top down sequencing of proteins. These data were acquired using a novel Quadrupole/TWIMS/oa-Tof mass spectrometer, operated with a nanoelectrospray ion source. The TWIMS is a stacked-ring ion guide, operated at elevated pressure, with opposite phases of an rf voltage applied to adjacent plates to provide radial ion confinement. A continual sequence of dc pulses is superimposed on the confining rf to provide ‘waves’ which propel ions through the gas. Protein species were ionised and the resulting ions separated based upon their ion mobility, or collision cross section, through the TWIMS device and subsequently mass analysed using the oa-TOF analyser.We have investigated the use of the hybrid ion mobility/ time-of-flight system for the top down analysis of proteins and compared these data with the data that can be obtained without an IMS separation. We have fragmented different charge states of the same protein and, by the post analysis selection of different regions of m/z vs drift time plots, produced spectral information which contains fragment ions of similar charge states. These selected regions can reveal species that are hidden in the non mobility experiment and these specific charge state spectra can be subsequently deconvoluted to produce sequence information. Typical increases in sequence coverage of around 20–25% are observed with a mobility enabled acquisition compared to a non mobility experiment.
机译:在本演示中,我们将展示离子淌度谱在蛋白质自上而下测序中的实用性。这些数据是使用新型的四极杆/ TWIMS / oa-Tof质谱仪获得的,该质谱仪与纳米电喷雾离子源一起操作。 TWIMS是一种叠环式离子导向器,可在升高的压力下运行,并且将射频电压的相反相位施加到相邻板上以提供径向离子限制。连续的直流脉冲序列叠加在限制射频上,以提供“波”,推动离子通过气体。通过TWIMS设备对蛋白质种类进行离子化处理,并根据其离子迁移率或碰撞截面将生成的离子分离,随后使用oa-TOF分析仪进行质量分析。我们研究了混合离子迁移率/分析时间的使用飞行系统进行蛋白质自上而下的分析,并将这些数据与无需进行IMS分离即可获得的数据进行比较。我们对同一蛋白质的不同电荷状态进行了分段,并通过后分析选择m / z与漂移时间图的不同区域,产生了包含相似电荷状态的碎片离子的光谱信息。这些选定的区域可以揭示非迁移性实验中隐藏的物种,并且这些特定的电荷状态谱可以随后进行反卷积以产生序列信息。与非移动性实验相比,启用移动性的采集可观察到典型的序列覆盖率增加约20–25%。

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