Literature DB >> 18262433

Reduction of axial kinetic energy induced perturbations on observed cyclotron frequency.

Nathan K Kaiser1, Chad R Weisbrod, Brian N Webb, James E Bruce.   

Abstract

With Fourier transform ion cyclotron resonance (FTICR) mass spectrometry one determines the mass-to-charge ratio of an ion by measuring its cyclotron frequency. However, the need to confine ions to the trapping region of the ion cyclotron resonance (ICR) cell with electric fields induces deviations from the unperturbed cyclotron frequency. Additional perturbations to the observed cyclotron frequency are often attributed to changes in space charge conditions. This study presents a detailed investigation of the observed ion cyclotron frequency as a function of ion z-axis kinetic energy. In a perfect three-dimensional quadrupolar field, cyclotron frequency is independent of position within the trap. However, in most ICR cell designs, this ideality is approximated only near the trap center and deviations arise from this ideal quadrupolar field as the ion moves both radially and axially from the center of the trap. To allow differentiation between deviations in observed cyclotron frequency caused from changes in space charge conditions or differences in oscillation amplitude, ions with identical molecular weights but different axial kinetic energy, and thus amplitude of z-axis motion, were simultaneously trapped within the ICR cell. This allows one to attribute deviations in observed cyclotron frequency to differences in the average force from the radial electric field experienced by ions of different axial amplitude. Experimentally derived magnetron frequency is compared with the magnetron frequency calculated using SIMION 7.0 for ions of different axial amplitude. Electron promoted ion coherence, or EPIC, is used to reduce the differences in radial electric fields at different axial positions. Thus with the application of EPIC, the differences in observed cyclotron frequencies are minimized for ions of different axial oscillation amplitudes.

Mesh:

Substances:

Year:  2008        PMID: 18262433      PMCID: PMC2387069          DOI: 10.1016/j.jasms.2007.12.009

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  18 in total

1.  A dynamic ion cooling technique for FTICR mass spectrometry.

Authors:  M V Gorshkov; C D Masselon; G A Anderson; H R Udseth; R Harkewicz; R D Smith
Journal:  J Am Soc Mass Spectrom       Date:  2001-11       Impact factor: 3.109

2.  Improved ion extraction from a linear octopole ion trap: SIMION analysis and experimental demonstration.

Authors:  Bruce E Wilcox; Christopher L Hendrickson; Alan G Marshall
Journal:  J Am Soc Mass Spectrom       Date:  2002-11       Impact factor: 3.109

3.  A mechanism for poor high mass performance in fourier transform mass spectrometry.

Authors:  C L Holliman; D L Rempel; M L Gross
Journal:  J Am Soc Mass Spectrom       Date:  1992-05       Impact factor: 3.109

4.  High-resolution accurate mass measurements of biomolecules using a new electrospray ionization ion cyclotron resonance mass spectrometer.

Authors:  B E Winger; S A Hofstadler; J E Bruce; H R Udseth; R D Smith
Journal:  J Am Soc Mass Spectrom       Date:  1993-07       Impact factor: 3.109

Review 5.  Fourier transform ion cyclotron resonance mass spectrometry: a primer.

Authors:  A G Marshall; C L Hendrickson; G S Jackson
Journal:  Mass Spectrom Rev       Date:  1998 Jan-Feb       Impact factor: 10.946

6.  A "screened" electrostatic ion trap for enhanced mass resolution, mass accuracy, reproducibility, and upper mass limit in Fourier transform ion cyclotron resonance mass spectrometry.

Authors:  M Wang; A G Marshall
Journal:  Anal Chem       Date:  1989-06-01       Impact factor: 6.986

7.  Detection of high-mass biomolecules in Fourier transform ion cyclotron resonance mass spectrometry: theoretical and experimental investigations.

Authors:  T Solouki; K J Gillig; D H Russell
Journal:  Anal Chem       Date:  1994-05-01       Impact factor: 6.986

8.  Proteomic profiling of intact proteins using WAX-RPLC 2-D separations and FTICR mass spectrometry.

Authors:  Seema Sharma; David C Simpson; Nikola Tolić; Navdeep Jaitly; Anoop M Mayampurath; Richard D Smith; Ljiljana Pasa-Tolić
Journal:  J Proteome Res       Date:  2007-02       Impact factor: 4.466

9.  Top-down approaches for measuring expression ratios of intact yeast proteins using Fourier transform mass spectrometry.

Authors:  Yi Du; Bryan A Parks; Seyoung Sohn; Kurt E Kwast; Neil L Kelleher
Journal:  Anal Chem       Date:  2006-02-01       Impact factor: 6.986

10.  Counting individual sulfur atoms in a protein by ultrahigh-resolution Fourier transform ion cyclotron resonance mass spectrometry: experimental resolution of isotopic fine structure in proteins.

Authors:  S D Shi; C L Hendrickson; A G Marshall
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-29       Impact factor: 11.205

View more
  4 in total

1.  Ion Behavior in an Electrically Compensated Ion Cyclotron Resonance Trap.

Authors:  Adam M Brustkern; Don L Rempel; Michael L Gross
Journal:  Int J Mass Spectrom       Date:  2011-03-01       Impact factor: 1.986

2.  Excite-coupled trapping ring electrode cell (eTREC): radial trapping field control, linearized excitation, and improved detection.

Authors:  Chad R Weisbrod; Nathan K Kaiser; Gunnar E Skulason; James E Bruce
Journal:  Anal Chem       Date:  2010-07-15       Impact factor: 6.986

3.  Trapping ring electrode cell: a FTICR mass spectrometer cell for improved signal-to-noise and resolving power.

Authors:  Chad R Weisbrod; Nathan K Kaiser; Gunnar E Skulason; James E Bruce
Journal:  Anal Chem       Date:  2008-08-06       Impact factor: 6.986

4.  The spontaneous loss of coherence catastrophe in Fourier transform ion cyclotron resonance mass spectrometry.

Authors:  Konstantin Aizikov; Raman Mathur; Peter B O'Connor
Journal:  J Am Soc Mass Spectrom       Date:  2008-10-17       Impact factor: 3.109

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.