High-resolution tandem mass spectrometry of large biomolecules.
Author(s) -
Joseph A. Loo,
J P Quinn,
Sunae Ryu,
Killian Henry,
Michael W. Senko,
Fred W. McLafferty
Publication year - 1992
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.89.1.286
Subject(s) - chemistry , mass spectrometry , dissociation (chemistry) , tandem mass spectrometry , mass spectrum , mass , ion , isotope , adduct , electrospray ionization , analytical chemistry (journal) , collision induced dissociation , electrospray , biomolecule , chromatography , organic chemistry , physics , biochemistry , quantum mechanics
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.
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