Ion Trap with Narrow Aperture Detection Electrodes for Fourier Transform Ion Cyclotron Resonance Mass Spectrometry
Ion Trap with Narrow Aperture Detection Electrodes for Fourier Transform Ion Cyclotron Resonance Mass Spectrometry
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用于傅里叶变换离子回旋共振质谱分析的具有窄孔径检测电极的离子阱
DOI:
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发表时间:
2015
影响因子:
3.2
通讯作者:
Y. O. Tsybin
中科院分区:
文献类型:
--
作者:
K. Nagornov;Anton N. Kozhinov;O. Tsybin;Y. O. Tsybin
AbstractThe current paradigm in ion trap (cell) design for Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) is the ion detection with wide aperture detection electrodes. Specifically, excitation and detection electrodes are typically 90° wide and positioned radially at a similar distance from the ICR cell axis. Here, we demonstrate that ion detection with narrow aperture detection electrodes (NADEL) positioned radially inward of the cell’s axis is feasible and advantageous for FT-ICR MS. We describe design details and performance characteristics of a 10 T FT-ICR MS equipped with a NADEL ICR cell having a pair of narrow aperture (flat) detection electrodes and a pair of standard 90° excitation electrodes. Despite a smaller surface area of the detection electrodes, the sensitivity of the NADEL ICR cell is not reduced attributable to improved excite field distribution, reduced capacitance of the detection electrodes, and their closer positioning to the orbits of excited ions. The performance characteristics of the NADEL ICR cell are comparable with the state-of-the-art FT-ICR MS implementations for small molecule, peptide, protein, and petroleomics analyses. In addition, the NADEL ICR cell’s design improves the flexibility of ICR cells and facilitates implementation of advanced capabilities (e.g., quadrupolar ion detection for improved mainstream applications). It also creates an intriguing opportunity for addressing the major bottleneck in FTMS—increasing its throughput via simultaneous acquisition of multiple transients or via generation of periodic non-sinusoidal transient signals.
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影响因子:
7.4
作者:
Williams, D. Keith, Jr.;Muddiman, David C.
通讯作者:
Muddiman, David C.
影响因子:
--
作者:
David von Lindenfels;Manuel Vogel;Gerhard Birkl;Wolfgang Quint;Marco Wiesel
通讯作者:
Marco Wiesel
影响因子:
7.4
作者:
Kilgour DP;Wills R;Qi Y;O'Connor PB
通讯作者:
O'Connor PB
影响因子:
7.4
作者:
McAlister, Graeme C.;Huttlin, Edward L.;Haas, Wilhelm;Ting, Lily;Jedrychowski, Mark P.;Rogers, John C.;Kuhn, Karsten;Pike, Ian;Grothe, Robert A.;Blethrow, Justin D.;Gygi, Steven P.
通讯作者:
Gygi, Steven P.
影响因子:
7.4
作者:
Weisbrod, Chad R.;Kaiser, Nathan K.;Skulason, Gunnar E.;Bruce, James E.
通讯作者:
Bruce, James E.