4.3 Article

Development of a new ion mobility (quadrupole) time-of-flight mass spectrometer

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INTERNATIONAL JOURNAL OF MASS SPECTROMETRY
卷 377, 期 -, 页码 655-662

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ELSEVIER SCIENCE BV
DOI: 10.1016/j.ijms.2014.07.034

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资金

  1. National Institute of General Medical Sciences [2 P41 GM 103493-11, 8 P41 GM103493-10, R21 GM103497]
  2. NIH National Center for Research Resources (NCRR) under ARRA award [3P41RR018522-07S1]
  3. National Cancer Institute [R21-CA12619-01, U24-CA-160019-01, Y01-CN-05013-29]
  4. National Institute of Environmental Health Sciences of the NIH [R01ES022190]
  5. Laboratory Directed Research and Development Program at Pacific Northwest National Laboratory
  6. U.S. Department of Energy Office of Biological and Environmental Research Genome Sciences Program under the Pan-omics project
  7. DOE [DE-AC05-76RL0 1830]
  8. American Reinvestment and Recovery Act

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A new ion mobility spectrometer (IMS) platform was developed to improve upon the sensitivity and reproducibility of our previous platforms, and further enhance IMS-MS utility for broad 'pan-omics' measurements. The new platform incorporated an improved electrospray ionization source and interface for enhanced sensitivity, and providing the basis for further benefits based upon implementation of multiplexed IMS. The ion optics included electrodynamic ion funnels at both the entrance and exit of the IMS, an ion funnel trap for ion injection, and a design in which nearly all ion optics (e.g., drift rings, ion funnels) were fabricated using printed circuit board technology. The IMS resolving power achieved was similar to 73 for singly-charged ions, very close to the predicted diffusion-limited resolving power (similar to 75). The platform's performance evaluation (e.g., for proteomics measurements) include LC-IMS-TOF MS datasets for 30 technical replicates for a trypsin digested human serum, and included platform performance in each dimension (LC, IMS and MS) separately. (C) 2014 Elsevier B.V. All rights reserved.

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