Comparison of mass spectra of peptides in different matrices using matrix-assisted laser desorption/ionization and a multi-turn time-of-flight mass spectrometer, MULTUM-IMG

The mass spectra of peptides obtained with different matrices were compared using a matrix‐assisted laser desorption/ionization (MALDI) ion source and a multi‐turn time‐of‐flight (TOF) mass spectrometer, MULTUM‐IMG, which has been developed at Osaka University. Two types of solid matrices, α‐cyano‐4‐hydroxycinnamic acid (CHCA) and 2,5‐dihydroxybenzoic acid (DHB), and a liquid matrix made from a mixture of 3‐aminoquinoline and CHCA were used. When measuring the peak signal intensity of human angiotensin II [M+H]+ from a fixed sample position, the liquid matrix produced a stable signal over 1000 laser shots, while the signal obtained with CHCA and DHB decayed after about 300 and 100 shots, respectively. Significant differences in the mass resolving power were not observed between the spectra obtained with the three matrices. Signal peak areas were measured as a function of the cycle number in a multi‐turn ion trajectory, i.e., the total flight time over a millisecond time scale. For both [M+H]+ of human angiotensin II and bovine insulin, the decay of the signal peak area was the most significant with CHCA, while that measured with DHB was the smallest. The results of the mean initial ion velocity measurements suggested that the extent of metastable decomposition of the analyte ions increased in order of DHB, the liquid matrix, and CHCA, which is consistent with the difference in the decay of the signal peak area as the total flight time increased. Copyright © 2008 John Wiley & Sons, Ltd.