Loo J A, Quinn J P, Ryu S I, Henry K D, Senko M W, McLafferty F W
Baker Chemistry Laboratory, Cornell University, Ithaca, NY 14853-1301.
Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):286-9. doi: 10.1073/pnas.89.1.286.
Unit-resolution mass spectra have been obtained for peptides as large as 17 kDa, providing information on impurities and adduct ions, as well as accurate molecular weight values. Electrospray ionization produces many multiply-charged species of the same mass; isotopic peak resolution provides direct charge state assignment from the unit mass spacing of the isotopes. This is of special value when the spectrum also has many masses, such as from precursor ion dissociation or impurities. Mass measuring errors not only are concomitantly lower (less than 0.1 Da) than when the isotopic peaks are unresolved but also are independent of variations in 13C/12C natural isotopic abundances. Also, larger errors are avoided that occur when the measured peak envelope includes impurity or adduct ions. This also benefits tandem mass spectrometry; dissociation of peptide ions as large as 8.5 kDa yields fragment masses consistent (less than 0.1 Da) with their amino acid sequences.
已获得分子量高达17 kDa的肽段的单位分辨率质谱图,该质谱图提供了有关杂质和加合离子的信息以及精确的分子量值。电喷雾电离会产生许多相同质量的多电荷物种;同位素峰分辨率可根据同位素的单位质量间距直接确定电荷状态。当质谱图中也有许多质量峰时,比如来自前体离子解离或杂质的质量峰,这一点具有特殊价值。质量测量误差不仅比同位素峰未解析时相应更低(小于0.1 Da),而且与13C/12C天然同位素丰度的变化无关。此外,当测量的峰包络包含杂质或加合离子时会出现较大误差,而现在可以避免这种情况。这对串联质谱分析也有益处;分子量高达8.5 kDa的肽离子解离产生的碎片质量与其氨基酸序列一致(小于0.1 Da)。