Iodoacetamide-alkylated methionine can mimic neutral loss of phosphoric acid from phosphopeptides as exemplified by nano-electrospray ionization quadrupole time-of-flight parent ion scanning-Reference-Cited by-同舟云学术

Iodoacetamide-alkylated methionine can mimic neutral loss of phosphoric acid from phosphopeptides as exemplified by nano-electrospray ionization quadrupole time-of-flight parent ion scanning

Published:2005 Issue:12 Volume:19 Page:1709-1716
ISSN:0951-4198
Container-title:Rapid Communications in Mass Spectrometry
language:en
Short-container-title:Rapid Commun. Mass Spectrom.

Author:

Krüger Ralf,Hung Chien-Wen,Edelson-Averbukh Marina,Lehmann Wolf D.

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference20 articles.

1. Neutral loss of amino acid residues from protonated peptides in collision-induced dissociation generates N- or C-terminal sequence ladders

2. Daughter ion mass spectra from cationized molecules of small oligopeptides in a reflecting time-of-flight mass spectrometer

3. C-Terminal Peptide Sequencing via Multistage Mass Spectrometry

4. Chromatographic and mass spectrometric methods for the identification of phosphorylation sites in phosphoproteins

5. Electrospray tandem mass spectrometric studies of phosphopeptides and phosphopeptide analogues

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