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本文引用的文献

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Gas-phase ion chromatography: transition metal state selection and carbon cluster formation.气相离子色谱法:过渡金属态选择和碳团簇形成。
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Chemically etched open tubular and monolithic emitters for nanoelectrospray ionization mass spectrometry.用于纳米电喷雾电离质谱的化学蚀刻开口管状和整体式发射器。
Anal Chem. 2006 Nov 15;78(22):7796-801. doi: 10.1021/ac061133r.
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Improving mass spectrometer sensitivity using a high-pressure electrodynamic ion funnel interface.使用高压电动离子漏斗接口提高质谱仪灵敏度。
J Am Soc Mass Spectrom. 2006 Sep;17(9):1299-305. doi: 10.1016/j.jasms.2006.06.005. Epub 2006 Jul 12.
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An IMS-IMS analogue of MS-MS.一种串联质谱(MS-MS)的离子淌度-离子淌度(IMS-IMS)类似物。
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5
IMS-IMS and IMS-IMS-IMS/MS for separating peptide and protein fragment ions.用于分离肽和蛋白质片段离子的离子淌度-离子淌度和离子淌度-离子淌度-串联质谱
Anal Chem. 2006 Apr 15;78(8):2802-9. doi: 10.1021/ac052208e.
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Variable low-mass filtering using an electrodynamic ion funnel.使用电动离子漏斗进行可变低质量过滤。
J Mass Spectrom. 2005 Sep;40(9):1215-22. doi: 10.1002/jms.900.
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High-sensitivity ion mobility spectrometry/mass spectrometry using electrodynamic ion funnel interfaces.使用电动离子漏斗接口的高灵敏度离子迁移谱/质谱联用技术。
Anal Chem. 2005 May 15;77(10):3330-9. doi: 10.1021/ac048315a.
8
Collisional activation of ions in RF ion traps and ion guides: the effective ion temperature treatment.射频离子阱和离子导向器中离子的碰撞激活:有效离子温度处理
J Am Soc Mass Spectrom. 2004 Nov;15(11):1616-28. doi: 10.1016/j.jasms.2004.07.014.
9
Application of peptide LC retention time information in a discriminant function for peptide identification by tandem mass spectrometry.肽段液相色谱保留时间信息在用于串联质谱肽段鉴定的判别函数中的应用。
J Proteome Res. 2004 Jul-Aug;3(4):760-9. doi: 10.1021/pr049965y.
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Characterization of the low molecular weight human serum proteome.低分子量人血清蛋白质组的表征
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使用电动离子漏斗和升高的漂移气体压力的离子迁移谱-质谱性能。

Ion mobility spectrometry-mass spectrometry performance using electrodynamic ion funnels and elevated drift gas pressures.

作者信息

Baker Erin Shammel, Clowers Brian H, Li Fumin, Tang Keqi, Tolmachev Aleksey V, Prior David C, Belov Mikhail E, Smith Richard D

机构信息

Biological Sciences Division and Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.

出版信息

J Am Soc Mass Spectrom. 2007 Jul;18(7):1176-87. doi: 10.1016/j.jasms.2007.03.031. Epub 2007 Apr 6.

DOI:10.1016/j.jasms.2007.03.031
PMID:17512752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3292285/
Abstract

The ability of ion mobility spectrometry coupled with mass spectrometry (IMS-MS) to characterize biological mixtures has been illustrated over the past eight years. However, the challenges posed by the extreme complexity of many biological samples have demonstrated the need for higher resolution IMS-MS measurements. We have developed a higher resolution ESI-IMS-TOF MS by utilizing high-pressure electrodynamic ion funnels at both ends of the IMS drift cell and operating the drift cell at an elevated pressure compared with that conventionally used. The ESI-IMS-TOF MS instrument consists of an ESI source, an hourglass ion funnel used for ion accumulation/injection into an 88 cm drift cell, followed by a 10 cm ion funnel and a commercial orthogonal time-of-flight mass spectrometer providing high mass measurement accuracy. It was found that the rear ion funnel could be effectively operated as an extension of the drift cell when the DC fields were matched, providing an effective drift region of 98 cm. The resolution of the instrument was evaluated at pressures ranging from 4 to 12 torr and ion mobility drift voltages of 16 V/cm (4 torr) to 43 V/cm (12 torr). An increase in resolution from 55 to 80 was observed from 4 to 12 torr nitrogen drift gas with no significant loss in sensitivity. The choice of drift gas was also shown to influence the degree of ion heating and relative trapping efficiency within the ion funnel.

摘要

在过去八年中,离子淌度光谱联用质谱(IMS-MS)表征生物混合物的能力已得到证实。然而,许多生物样品的极端复杂性带来的挑战表明,需要进行更高分辨率的IMS-MS测量。我们通过在IMS漂移池的两端使用高压电动离子漏斗,并将漂移池在高于传统使用压力的条件下运行,开发出了一种更高分辨率的电喷雾电离-离子淌度-飞行时间质谱仪(ESI-IMS-TOF MS)。该ESI-IMS-TOF MS仪器由一个电喷雾电离源、一个用于离子积累/注入到88厘米漂移池的沙漏形离子漏斗、一个10厘米的离子漏斗以及一台提供高质量测量精度的商用正交飞行时间质谱仪组成。研究发现,当直流电场匹配时,后置离子漏斗可作为漂移池的有效延伸,从而提供98厘米的有效漂移区域。在4至12托的压力范围以及16伏/厘米(4托)至43伏/厘米(12托)的离子淌度漂移电压下对仪器的分辨率进行了评估。在4至12托的氮气漂移气体中,观察到分辨率从55提高到了80,且灵敏度没有显著损失。还表明漂移气体的选择会影响离子加热程度以及离子漏斗内的相对俘获效率。