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本文引用的文献

1
Native Mass Spectrometry: What is in the Name?原生质谱:名称有何含义?
J Am Soc Mass Spectrom. 2017 Jan 1;28(1):5-13. doi: 10.1021/jasms.8b05378.
2
New insights into the metal-induced oxidative degradation pathways of transthyretin.新型金属诱导转甲状腺素蛋白氧化降解途径研究进展
Chem Commun (Camb). 2019 Apr 2;55(28):4091-4094. doi: 10.1039/c9cc00682f.
3
Topological Analysis of Transthyretin Disassembly Mechanism: Surface-Induced Dissociation Reveals Hidden Reaction Pathways.转甲状腺素蛋白解组装机制的拓扑分析:表面诱导的解离揭示了隐藏的反应途径。
Anal Chem. 2019 Feb 5;91(3):2345-2351. doi: 10.1021/acs.analchem.8b05066. Epub 2019 Jan 28.
4
Effect of droplet lifetime on where ions are formed in electrospray ionization.液滴寿命对电喷雾电离中离子形成位置的影响。
Analyst. 2018 Dec 17;144(1):237-248. doi: 10.1039/c8an01824c.
5
Fourier Transform-Ion Mobility-Orbitrap Mass Spectrometer: A Next-Generation Instrument for Native Mass Spectrometry.傅里叶变换离子淌度-轨道阱质谱仪:用于天然质谱的下一代仪器。
Anal Chem. 2018 Sep 4;90(17):10472-10478. doi: 10.1021/acs.analchem.8b02463. Epub 2018 Aug 22.
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Development and Evaluation of a Reverse-Entry Ion Source Orbitrap Mass Spectrometer.一种反向进样离子源轨道阱质谱仪的研制与评价。
J Am Soc Mass Spectrom. 2019 Jan;30(1):192-198. doi: 10.1007/s13361-018-1976-0. Epub 2018 May 23.
7
Identification of Lasso Peptide Topologies Using Native Nanoelectrospray Ionization-Trapped Ion Mobility Spectrometry-Mass Spectrometry.利用天然纳升电喷雾离子化-离子淌度谱-质谱鉴定拉索肽拓扑结构。
Anal Chem. 2018 Apr 17;90(8):5139-5146. doi: 10.1021/acs.analchem.7b05230. Epub 2018 Apr 3.
8
Allostery revealed within lipid binding events to membrane proteins.变构作用揭示了膜蛋白与脂类结合事件中的变构现象。
Proc Natl Acad Sci U S A. 2018 Mar 20;115(12):2976-2981. doi: 10.1073/pnas.1719813115. Epub 2018 Mar 5.
9
Fourier Transform-Ion Cyclotron Resonance Mass Spectrometry as a Platform for Characterizing Multimeric Membrane Protein Complexes.傅里叶变换离子回旋共振质谱作为一种用于鉴定多聚体膜蛋白复合物的平台。
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Characterizing the Conformationome: Toward a Structural Understanding of the Proteome.描绘构象组学:迈向对蛋白质组结构的理解。
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原生离子淌度-轨道阱质谱:揭示隐藏之物

Native IM-Orbitrap MS: Resolving What Was Hidden.

作者信息

Poltash Michael L, McCabe Jacob W, Shirzadeh Mehdi, Laganowsky Arthur, Russell David H

机构信息

Department of Chemistry, Texas A&M University, 3255 TAMU, College Station, Texas 77843.

出版信息

Trends Analyt Chem. 2020 Mar;124. doi: 10.1016/j.trac.2019.05.035. Epub 2019 May 31.

DOI:10.1016/j.trac.2019.05.035
PMID:32189816
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7079669/
Abstract

Native ion mobility-mass spectrometry (IM-MS) is an emerging biophysical approach to probe the intricate details of protein structure and function. The instrument design enables measurements of accurate first-principle determinations of rotationally-averaged ion-neutral collision cross sections coupled with high-mass, high-resolution mass measurement capabilities of Orbitrap MS. The inherent duty-cycle mismatch between drift tube IM and Orbitrap MS is alleviated by operating the drift tube in a frequency modulated mode while continuously acquiring mass spectra with the Orbitrap MS. Fourier transform of the resulting time-domain signal, i.e., ion abundances as a function of the modulation frequency, yields a frequency domain spectrum that is then converted (s to s) to IM drift time. This multiplexed approach allows for a duty-cycle of 25% compared to <1% for traditional "pulse-and-wait" IM-ToF-MS. Improvements in mobility and mass resolution of the IM-Orbitrap allows for accurate analysis of intact protein complexes and the possibility of capturing protein dynamics.

摘要

原生离子淌度-质谱联用(IM-MS)是一种新兴的生物物理方法,用于探究蛋白质结构和功能的复杂细节。该仪器设计能够测量旋转平均离子-中性碰撞截面的精确第一性原理测定值,并结合了Orbitrap质谱仪的高质量、高分辨率质量测量能力。通过在调频模式下操作漂移管,同时利用Orbitrap质谱仪连续采集质谱,缓解了漂移管离子淌度谱与Orbitrap质谱仪之间固有的占空比不匹配问题。对所得时域信号(即作为调制频率函数的离子丰度)进行傅里叶变换,得到频域谱,然后将其转换(秒到秒)为离子淌度漂移时间。与传统的“脉冲等待”IM-TOF-MS小于1%的占空比相比,这种复用方法允许25%的占空比。IM-Orbitrap在淌度和质量分辨率方面的改进,使得能够对完整的蛋白质复合物进行精确分析,并有可能捕捉蛋白质动力学。