Abstract
Charge detection mass spectrometry (CDMS) allows direct mass measurement of
heterogeneous samples by simultaneously determining the charge state and the mass-to-
charge ratio (m/z) of individual ions, unlike conventional MS methods that use large ensembles
of ions. CDMS typically requires long acquisition times and the collection of thousands of
spectra, each containing tens to hundreds of ions, to generate sufficient ion statistics, making it
difficult to interface with the time scales of online separation techniques such as ion mobility.
Here, we demonstrate the application of Fourier transform multiplexing and drift tube ion
mobility joined with Orbitrap-based CDMS for the analysis of multimeric protein complexes.
Stepped frequency modulation was utilized to enable unambiguous frequency assignment
during mobility sweeps and allow spectral averaging, which improves the accuracy and signal to
noise of arrival time distributions and CDMS measurements. Fourier transformation of the
signal reveals the arrival times and collision cross sections of ions while simultaneously
collecting charge information for thousands of individual ions. Combining Fourier transform
multiplexing ion mobility and CDMS provides insight into each ion’s size and mass while
showcasing a potential solution to the duty cycle mismatch of online separation techniques in
the single ion regime.
Supplementary materials
Title
Supporting Figures
Description
Additional tables, arrival time distributions, intact mass, and charge distributions
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