4.3 Article

FT-ICR MS optimization for the analysis of intact proteins

Journal

INTERNATIONAL JOURNAL OF MASS SPECTROMETRY
Volume 287, Issue 1-3, Pages 32-38

Publisher

ELSEVIER
DOI: 10.1016/j.ijms.2008.10.010

Keywords

FT-ICR; Top-down proteomics; Dynamic range; Resolution; Mass accuracy

Funding

  1. National Center for Research Resources [RR 018522]
  2. National Institute of Allergy and Infectious Diseases NIH/DHHS [Y1-AI-4894-01]
  3. National Institute of General Medical Sciences NIGMS [R01 GM063883]
  4. U.S. Department of Energy (DOE) Office of Biological and Environmental Research
  5. DOE [DE-AC05-76RLO 1830]

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Fourier-transform ion cyclotron resonance (FT-ICR) mass spectrometry (MS) remains the technique of choice for the analysis of intact proteins from complex biological systems, i.e., top-down proteomics. Recently, we have implemented a compensated open cylindrical ion trapping cell into a 12 T Fr-ICR mass spectrometer. This new cell has previously demonstrated improved sensitivity, dynamic range, and mass measurement accuracy for the analysis of relatively small tryptic peptides. These improvements are due to the modified trapping potential of the cell which closely approximates the ideal harmonic trapping potential. Here, we report the instrument optimization for the analysis of large macro-molecular ions, such as proteins. Single transient mass spectra of multiply charged bovine ubiquitin ions with sub-ppm mass measurement accuracy, improved signal intensity, and increased dynamic range were obtained using this new cell with increased post-excitation cyclotron radii. The increased cyclotron radii correspond to increased ion kinetic energy and collisions between neutrals and ions with sufficient kinetic energy can exceed a threshold of single collision ion fragmentation. A transition then occurs from relatively long signal lifetimes at low excitation radii to potentially shorter lifetimes, defined by the average ion-neutral collision time. The proposed high energy ion loss mechanism is evaluated and compared with experimental results for bovine ubiquitin and serum albumin. We find that the analysis of large macromolecules can be significantly improved by the further reduction of pressure in the ion trapping cell. This reduces the high energy ion losses and can enable increased sensitivity and mass measurement accuracy to be realized without compromising resolution. Further, these results appear to be generally applicable to FTMS, and it is expected that the high energy ion loss mechanism also applies to Orbitrap mass analyzers. (C) 2008 Elsevier B.V. All rights reserved.

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