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一种具有三个用于离子/离子反应的离子源的离子阱-离子淌度-飞行时间质谱仪。

An ion trap-ion mobility-time of flight mass spectrometer with three ion sources for ion/ion reactions.

作者信息

Zhao Qin, Soyk Matthew W, Schieffer Gregg M, Fuhrer Katrin, Gonin Marc M, Houk R S, Badman Ethan R

机构信息

Department of Chemistry, Iowa State University, Ames, Iowa, USA.

出版信息

J Am Soc Mass Spectrom. 2009 Aug;20(8):1549-61. doi: 10.1016/j.jasms.2009.04.014. Epub 2009 May 4.

Abstract

This instrument combines the capabilities of ion/ion reactions with ion mobility (IM) and time-of-flight (TOF) measurements for conformation studies and top-down analysis of large biomolecules. Ubiquitin ions from either of two electrospray ionization (ESI) sources are stored in a three dimensional (3D) ion trap (IT) and reacted with negative ions from atmospheric sampling glow discharge ionization (ASGDI). The proton transfer reaction products are then separated by IM and analyzed via a TOF mass analyzer. In this way, ubiquitin +7 ions are converted to lower charge states down to +1; the ions in lower charge states tend to be in compact conformations with cross sections down to approximately 880 A(2). The duration and magnitude of the ion ejection pulse on the IT exit and the entrance voltage on the IM drift tube can affect the measured distribution of conformers for ubiquitin +7 and +6. Alternatively, protein ions are fragmented by collision-induced dissociation (CID) in the IT, followed by ion/ion reactions to reduce the charge states of the CID product ions, thus simplifying assignment of charge states and fragments using the mobility-resolved tandem mass spectrum. Instrument characteristics and the use of a new ion trap controller and software modifications to control the entire instrument are described.

摘要

该仪器将离子/离子反应能力与离子淌度(IM)和飞行时间(TOF)测量相结合,用于大生物分子的构象研究和自上而下分析。来自两个电喷雾电离(ESI)源中任意一个的泛素离子被存储在三维(3D)离子阱(IT)中,并与来自大气采样辉光放电电离(ASGDI)的负离子发生反应。然后,质子转移反应产物通过离子淌度进行分离,并通过飞行时间质谱仪进行分析。通过这种方式,泛素 +7 离子被转化为低至 +1 的较低电荷态;较低电荷态的离子往往处于紧凑构象,其截面低至约 880 Ų。离子阱出口处的离子喷射脉冲持续时间和幅度以及离子淌度漂移管上的入口电压会影响所测量的泛素 +7 和 +6 构象体分布。或者,蛋白质离子在离子阱中通过碰撞诱导解离(CID)进行碎裂,随后进行离子/离子反应以降低 CID 产物离子的电荷态,从而使用淌度分辨串联质谱简化电荷态和碎片的归属。文中描述了仪器特性以及使用新型离子阱控制器和软件修改来控制整个仪器的情况。

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