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Gated Trapped Ion Mobility Spectrometry Coupled to Fourier Transform Ion Cyclotron Resonance Mass Spectrometry

机译:门控陷阱离子淌度光谱与傅立叶变换离子回旋共振质谱联用

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摘要

Analysis of molecules by ion mobility spectrometry coupled with mass spectrometry (IMS-MS) provides chemical information on the three dimensional structure and mass of the molecules. The coupling of ion mobility to trapping mass spectrometers has historically been challenging due to the large differences in analysis time between the two devices. In this paper we present a modification of the trapped ion mobility (TIMS) analysis scheme termed “Gated TIMS” that allows efficient coupling to a Fourier Transform Ion Cyclotron Resonance (FT-ICR) analyzer. Analyses of standard compounds and the influence of source conditions on the TIMS distributions produced by ion mobility spectra of labile ubiquitin protein ions are presented. Ion mobility resolving powers up to 100 are observed. Measured collisional cross sections of ubiquitin ions are in excellent qualitative and quantitative agreement to previous measurements. Gated TIMS FT-ICR produces results comparable to those acquired using TIMS/time-of-flight MS instrument platforms as well as numerous drift tube IMS-MS studies published in the literature.
机译:通过离子迁移谱与质谱(IMS-MS)结合对分子进行分析,可提供有关分子的三维结构和质量的化学信息。由于两种设备之间的分析时间差异很大,因此离子迁移率与捕集质谱仪的耦合历来一直很困难。在本文中,我们介绍了一种被称为“门控TIMS”的捕获离子迁移率(TIMS)分析方案的改进方案,该方案可以有效耦合至傅立叶变换离子回旋共振(FT-ICR)分析仪。提出了标准化合物的分析以及源条件对不稳定的泛素蛋白离子的离子迁移谱产生的TIMS分布的影响。观察到高达100的离子淌度分辨能力。测量的泛素离子的碰撞截面与先前的测量在定性和定量方面都非常吻合。门控TIMS FT-ICR产生的结果可与使用TIMS /飞行时间MS仪器平台以及文献中发表的大量漂移管IMS-MS研究获得的结果相媲美。

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