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在离子阱离子淌度装置中肽和蛋白质离子的碎片化和迁移率分离。

Fragmentation and Mobility Separation of Peptide and Protein Ions in a Trapped-Ion Mobility Device.

机构信息

Department of Chemistry, University of Nevada, 1664 N. Virginia Street, Reno, Nevada 89557, United States.

出版信息

Anal Chem. 2021 Jul 27;93(29):9959-9964. doi: 10.1021/acs.analchem.1c01188. Epub 2021 Jul 14.

Abstract

Ion mobility separations (IMS) have increasingly been coupled with mass spectrometry to increase peak capacity and deconvolute complex mass spectra in proteomics workflows. IMS separations can be integrated prior to or following the collisional activation step. Post-activation IMS separations have demonstrated many advantages, yet few instrument platforms are capable of this feat. Here, we present the fragmentation of peptide ions within a commercially available trapped-ion mobility spectrometry device. Fragmentation is initiated prior to mobility analysis enabling the separation of generated product ions. The added separation step deconvolutes product ion spectra and permits improved annotation of product ions. Furthermore, we demonstrate the isolation and fragmentation of mobility separated product ions with the downstream quadrupole and collisional cell. When applied to melittin and ubiquitin, this ion mobility assisted pseudo-MS fragmentation approach generates sequence coverage ∼50% greater than that of typical MS analyses. We envision this ion-mobility-assisted fragmentation technique as the foundation of a powerful new pseudo-MS workflow for application toward middle- or top-down proteomics.

摘要

离子淌度分离(IMS)越来越多地与质谱联用,以增加蛋白质组学工作流程中的峰容量和解卷积复杂的质谱。IMS 分离可以在碰撞激活步骤之前或之后进行集成。激活后的 IMS 分离具有许多优点,但很少有仪器平台能够实现这一壮举。在这里,我们在商业上可用的俘获离子淌度谱仪设备内展示了肽离子的碎裂。在进行淌度分析之前启动碎裂,从而实现生成的产物离子的分离。附加的分离步骤解卷积产物离子谱,并允许更好地注释产物离子。此外,我们还演示了通过下游四极杆和碰撞池对淌度分离的产物离子进行的隔离和碎裂。当应用于蜂毒素和泛素时,这种离子淌度辅助的拟 MS 碎裂方法产生的序列覆盖率比典型 MS 分析高约 50%。我们设想这种离子淌度辅助的碎裂技术是一种强大的新拟 MS 工作流程的基础,可用于中间或自上而下的蛋白质组学。

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