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Anal Chem. 2016 Jan 19;88(2):1162-8. doi: 10.1021/acs.analchem.5b02987. Epub 2015 Dec 24.

Parallel Spectral Acquisition with an Ion Cyclotron Resonance Cell Array.

Author information

1
Department of Genome Sciences, University of Washington , Seattle, Washington 98109, United States.
2
GAA Custom Engineering, LLC, Benton City, Washington 99320, United States.

Abstract

Mass measurement accuracy is a critical analytical figure-of-merit in most areas of mass spectrometry application. However, the time required for acquisition of high-resolution, high mass accuracy data limits many applications and is an aspect under continual pressure for development. Current efforts target implementation of higher electrostatic and magnetic fields because ion oscillatory frequencies increase linearly with field strength. As such, the time required for spectral acquisition of a given resolving power and mass accuracy decreases linearly with increasing fields. Mass spectrometer developments to include multiple high-resolution detectors that can be operated in parallel could further decrease the acquisition time by a factor of n, the number of detectors. Efforts described here resulted in development of an instrument with a set of Fourier transform ion cyclotron resonance (ICR) cells as detectors that constitute the first MS array capable of parallel high-resolution spectral acquisition. ICR cell array systems consisting of three or five cells were constructed with printed circuit boards and installed within a single superconducting magnet and vacuum system. Independent ion populations were injected and trapped within each cell in the array. Upon filling the array, all ions in all cells were simultaneously excited and ICR signals from each cell were independently amplified and recorded in parallel. Presented here are the initial results of successful parallel spectral acquisition, parallel mass spectrometry (MS) and MS/MS measurements, and parallel high-resolution acquisition with the MS array system.

PMID:
26669509
PMCID:
PMC4848028
DOI:
10.1021/acs.analchem.5b02987
[Indexed for MEDLINE]
Free PMC Article

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