The recently developed FAB/MSMS methodology ( i.e. ) ionization of an underivatized peptide by using fast‐atom‐bombardment (FAB) combined with tandem mass spectrometry (MSMS) is applied for the sequencing of the cyclotetrapeptide tentoxin ( 12 ). The scope and limitation of the strategy is discussed in detail. Possible resolutions to overcome problems related to ( i ) the resolution of isobaric fragment ions and ( ii ) the distinction of sequence vs. retro ‐sequence are investigated. The novel strategy is compared with conventional techniques. Significant improvement of the presently used FAB/MSMS methodology can be achieved by combining this approach with accurate mass measurements.
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Eckart et al. (1987) studied this question.
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