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在电喷雾电离傅里叶变换静电线性离子阱质谱中高次谐波的应用。

Utility of Higher Harmonics in Electrospray Ionization Fourier Transform Electrostatic Linear Ion Trap Mass Spectrometry.

机构信息

Department of Chemistry, Purdue University , West Lafayette, Indiana 47907-2084, United States.

出版信息

Anal Chem. 2017 Apr 18;89(8):4392-4397. doi: 10.1021/acs.analchem.7b00034. Epub 2017 Mar 30.

DOI:10.1021/acs.analchem.7b00034
PMID:28326764
Abstract

Mass resolution (M/ΔM fwhm) is observed to linearly increase with harmonic order in a Fourier transform electrostatic linear ion trap (ELIT) mass spectrometer. This behavior was predicted by Grosshans and Marshall for frequency-multiple detection in a Fourier transform ion cyclotron resonance mass spectrometer only for situations when the prominent mechanism for signal decay is ion ejection from the trap. As the analyzer pressure in our ELIT chamber is relatively high, such that collisional scattering and collision-induced dissociation are expected to underlie much of the ion loss, we sought to explore the relationship between harmonic order and mass resolution. Mass resolutions of 36 900 (fundamental), 75 850 (2nd harmonic), and 108 200 (3rd harmonic) were obtained for GdO (avg. m/z 173.919) with a transient length of 300 ms. To demonstrate that the mass resolution was truly increasing with harmonic order, the unresolved isotopes at the fundamental distribution of cytochrome c (m/z ∼ 1549) were nearly baseline, resolved at the third harmonic (mass resolution ≈ 23 000) with a transient length of only 200 ms. This experiment demonstrates that, when the ion density is sufficiently low, ions with frequency differences of less than 4 Hz remain uncoalesced. Higher harmonics can be used to increase the effective mass resolution for a fixed transient length and thereby may enable the resolution of closely spaced masses, determination of a protein ion's charge state, and study of the onset of peak coalescence when the resolution at the fundamental frequency is insufficient.

摘要

在傅里叶变换静电线性离子阱(ELIT)质谱仪中,质量分辨率(M/ΔM fwhm)观察到随着谐波阶数呈线性增加。这种行为仅在信号衰减的主要机制是从阱中逐出离子的情况下,由 Grosshans 和 Marshall 预测在傅里叶变换离子回旋共振质谱仪中进行频率多次检测时会出现。由于我们的 ELIT 腔中的分析器压力相对较高,因此预计碰撞散射和碰撞诱导解离将构成大部分离子损失的基础,我们试图探索谐波阶数和质量分辨率之间的关系。对于 GdO(平均 m/z 173.919),瞬变长度为 300 ms 时,获得了 36900(基频)、75850(二次谐波)和 108200(三次谐波)的质量分辨率。为了证明质量分辨率确实随着谐波阶数的增加而增加,在瞬变长度仅为 200 ms 的情况下,使用三次谐波几乎可以完全分辨出细胞色素 c(m/z∼1549)基频分布中未解析的同位素(质量分辨率≈23000)。该实验表明,当离子密度足够低时,频率差小于 4 Hz 的离子仍未聚结。更高的谐波可以用于在固定的瞬变长度下增加有效质量分辨率,从而可以实现紧密间隔质量的分辨率、确定蛋白质离子的电荷状态以及在基本频率的分辨率不足时研究峰聚结的开始。

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