Mw. Senko et al., ELECTROSPRAY-IONIZATION FOURIER-TRANSFORM ION-CYCLOTRON RESONANCE AT 9.4 T, Rapid communications in mass spectrometry, 10(14), 1996, pp. 1824-1828
We present the first results from a new electrospray ionization Fourie
r transform ion cyclotron resonance mass spectrometer operated at a ma
gnetic field of 9.4 T (i.e. greater than or equal to 2.4 T higher than
for any prior FTICR instrument). The 9.4 T instrument provides substa
ntially Improved performance for large molecules (greater than or equa
l to 50% increase in mass resolving power) and complex mixtures (great
er than or equal to 100% increase in dynamic range) compared to lower-
field (less than or equal to 6 T) instruments, The higher magnetic fie
ld makes possible larger trapped-ion population without introduction o
f significant space-charge effects such as spectral peak shift and/or
distortion, and coalescence of closely-spaced resonances, For bovine u
biquitin (8.6 kDa) we observe accurate relative isotopic abundances at
a signal-to-noise ratio greater than 1000:1, whereas a complete nozzl
e-skimmer dissociation electrospray ionization (ESI) FTICR mass spectr
um of bovine carbonic anhydrase (29 kDa) is achieved from a single sca
n with a signal-to-noise ratio of more than 250:1, Finally, we are abl
e to obtain mass resolving power, m/Delta m >200 000, routinely for po
rcine serum albumin (67 kDa). The present performance guides further m
odifications of the instrument, which should lead to significant furth
er improvements.