Je. Bruce et al., TRAPPING, DETECTION, AND MASS MEASUREMENT OF INDIVIDUAL IONS IN A FOURIER-TRANSFORM ION-CYCLOTRON RESONANCE MASS-SPECTROMETER, Journal of the American Chemical Society, 116(17), 1994, pp. 7839-7847
A Fourier transform ion cyclotron resonance (FTICR) mass spectrometer
has been used to trap individual multiply charged ions of several high
molecular weight polymers, including poly(ethylene oxide), sodium pol
y(styrene sulfonate), and the protein bovine serum albumin. Detection
of these ions is performed with the nondestructive method distinctive
of FTICR, which also allows remeasurement of the same ion or ion popul
ation over several hours. For the determination of the charge states (
and hence the masses) of individual ions, a new scheme was developed o
n the basis of the observation of the stepwise mit shifts that result
from charge exchange reactions or adduction of a substance of known ma
ss. A novel technique for mass determination of individual ions has be
en made possible with the observation of cyclotron frequency shifts du
ring the time-domain acquisition period. This time-resolved ion correl
ation (TRIC) technique allows reactant and product ions to be correlat
ed with confidence and provides the basis for simultaneously studying
a moderate number of ions. In this work, a range of observations relat
ed to the detection and measurement of Individual ions is presented, a
s are examples of mass determinations of individual ions performed by
utilizing the TRIC technique. Results are presented that show the meas
urement of poly(ethylene glycol) (PEG) individual ions of more than 5
MDa with more than 2500 net charges and measurement of ions as small a
s albumin (66 kDa) with as few as 30 charges. Other results illustrate
that unexpected behavior can be observed for individual ions that wou
ld not be apparent in large ion populations.