Ultrahigh Resolution Ion Isolation by Stored Waveform Inverse Fourier Transform 21 T Fourier Transform Ion Cyclotron Resonance Mass Spectrometry

被引:16
|
作者
Smith, Donald F. [1 ]
Blakney, Greg T. [1 ]
Beu, Steven C. [3 ]
Anderson, Lissa C. [1 ]
Weisbrod, Chad R. [1 ]
Hendrickson, Christopher L. [1 ,2 ]
机构
[1] Florida State Univ, Natl High Magnet Field Lab, 1800 East Paul Dirac Dr, Tallahassee, FL 32310 USA
[2] Florida State Univ, Dept Chem & Biochem, 95 Chieftain Way, Tallahassee, FL 32310 USA
[3] SC Beu Consulting, 12449 Los Indios Trail, Austin, TX 78729 USA
基金
美国国家科学基金会;
关键词
COLLISION-INDUCED DISSOCIATION; PHASE MODULATION; EXCITATION; IDENTIFICATION; FRAGMENTATION; PROTEOFORMS; SELECTION; SPECTRA;
D O I
10.1021/acs.analchem.9b04954
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Stored waveform inverse Fourier transform (SWIFT) is a versatile method to generate complex isolation/ejection waveforms for precursor isolation prior to tandem mass spectrometry experiments. Here, we report ultrahigh resolving power ion isolation by SWIFT on a 21 T Fourier transform ion cyclotron resonance (FTICR) mass spectrometer. Individual histone proteoforms are isolated (0.6 m/z isolation window) with near 100% efficiency using a 52 ms SWIFT isolation, followed by in-cell fragmentation by ultraviolet photodissociation (UVPD). Ion isolation resolving power of 175 000 (m/Delta m) is demonstrated by isolation of individual peaks at a spacing of 0.0034 Da at m/z 597 from a complex mixture of Canadian bitumen. An individual m/z ion, which corresponds to a single elemental composition, from a complex mixture is isolated and fragmented by infrared multiphoton dissociation (IRMPD). Theoretical and experimental considerations that limit achievable ion isolation resolving power are discussed.
引用
收藏
页码:3213 / 3219
页数:7
相关论文
共 50 条
  • [1] Fourier transform ion cyclotron resonance mass spectrometry
    Marshall, AG
    [J]. FOURIER TRANSFORM SPECTROSCOPY, 1998, (430): : 3 - 13
  • [2] GENERAL PHASE MODULATION METHOD FOR STORED WAVEFORM INVERSE FOURIER-TRANSFORM EXCITATION FOR FOURIER-TRANSFORM ION-CYCLOTRON RESONANCE MASS-SPECTROMETRY
    GUAN, SH
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1989, 91 (02): : 775 - 777
  • [3] Fourier Transform Ion Cyclotron Resonance Mass Spectrometry at the Cyclotron Frequency
    Nagornov, Konstantin O.
    Kozhinov, Anton N.
    Tsybin, Yury O.
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2017, 28 (04) : 768 - 780
  • [4] Fourier transform ion cyclotron resonance mass spectrometry: A primer
    Marshall, AG
    Hendrickson, CL
    Jackson, GS
    [J]. MASS SPECTROMETRY REVIEWS, 1998, 17 (01) : 1 - 35
  • [5] Fourier transform ion cyclotron resonance mass spectrometry - Preface
    Marshall, AG
    [J]. INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1996, 157 : R9 - R11
  • [7] Quantitation of ion abundances in Fourier transform ion cyclotron resonance mass spectrometry
    Goodner, KL
    Milgram, KE
    Williams, KR
    Watson, CH
    Eyler, JR
    [J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1998, 9 (11) : 1204 - 1212
  • [8] Compositional Analysis of Oil Residues by Ultrahigh-Resolution Fourier Transform Ion Cyclotron Resonance Mass Spectrometry
    Kekalainen, Timo
    Pakarinen, Jaana M. H.
    Wickstrom, Kim
    Lobodin, Vladislav V.
    McKenna, Amy M.
    Janis, Janne
    [J]. ENERGY & FUELS, 2013, 27 (04) : 2002 - 2009
  • [9] Asphaltene Characterization during Hydroprocessing by Ultrahigh-Resolution Fourier Transform Ion Cyclotron Resonance Mass Spectrometry
    Rogel, Estrella
    Witt, Matthias
    [J]. ENERGY & FUELS, 2017, 31 (04) : 3409 - 3416
  • [10] Precision in Petroleomics via Ultrahigh Resolution Electrospray Ionization Fourier Transform Ion Cyclotron Resonance Mass Spectrometry
    Pereira, Rosana C. L.
    Simas, Rosineide C.
    Corilo, Yuri E.
    Vaz, Boniek G.
    Klitzke, Clecio F.
    Schmidt, Eduardo M.
    Pudenzi, Marcos A.
    Silva, Raissa M. C. F.
    Moraes, Erica T.
    Bastos, Wagner L.
    Eberlin, Marcos N.
    Lopes Nascimento, Heliara D.
    [J]. ENERGY & FUELS, 2013, 27 (12) : 7208 - 7216