ULTRAHIGH MASS ACCURACY IN ISOTOPE-SELECTIVE COLLISION-INDUCED DISSOCIATION USING CORRELATED SWEEP EXCITATION AND SUSTAINED OFF-RESONANCE IRRADIATION - A FOURIER-TRANSFORM ION-CYCLOTRON RESONANCE MASS-SPECTROMETRY CASE-STUDY ON THE [M+2H](2+) ION OF BRADYKININ
Ajr. Heck et Pj. Derrick, ULTRAHIGH MASS ACCURACY IN ISOTOPE-SELECTIVE COLLISION-INDUCED DISSOCIATION USING CORRELATED SWEEP EXCITATION AND SUSTAINED OFF-RESONANCE IRRADIATION - A FOURIER-TRANSFORM ION-CYCLOTRON RESONANCE MASS-SPECTROMETRY CASE-STUDY ON THE [M+2H](2+) ION OF BRADYKININ, Analytical chemistry, 69(17), 1997, pp. 3603-3607
Using electrospray ionization with a 9.4 T Fourier transform mass spec
trometer, fragment ion spectra were acquired for a single isotopomer o
f doubly protonated bradykinin (molecular mass, 1059.6 Da). Correlated
sweep excitation methods were applied to mass-select the single isoto
pomer (m/z = 530.8), Sustained off-resonance irradiation was used to a
ctivate and fragment the ions. The accuracy (in terms of m/z) in detec
tion of the fragment ions was on average 1.2 ppm, making the assignmen
ts unambiguous. The methods employed would be generally applicable to
ions in the mass range of approximately 50 Da to 50 kDa.