Literature DB >> 15627961

Analysis of thyroglobulin iodination by tandem mass spectrometry using immonium ions of monoiodo- and diiodo-tyrosine.

Mogjiborahman Salek1, Wolf D Lehmann.   

Abstract

Peptides containing a monoiodo- or diiodo-tyrosine residue (monoiodo-Y, diiodo-Y) were found to generate abundant immonium ions following collision-induced dissociation at m/z 261.97 and 387.87 Da, respectively. These residue-specific marker ions are between about 140 mDa (monoiodo-Y) and 300 mDa (diiodo-Y) mass deficient relative to any other peptide fragment ions of unmodified peptides, qualifying them as highly specific marker ions for tyrosine iodination when analyzed by high resolution tandem mass spectrometry (MS/MS). Two new iodination sites (Y-364 and Y-2165) were pinpointed in bovine thyroglobulin by MS/MS using these iodotyrosine-specific marker ions and combined tryptic/chymotryptic digestion.

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Year:  2005        PMID: 15627961     DOI: 10.1002/pmic.200400949

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  3 in total

1.  Revisiting iodination sites in thyroglobulin with an organ-oriented shotgun strategy.

Authors:  Alain Dedieu; Jean-Charles Gaillard; Thierry Pourcher; Elisabeth Darrouzet; Jean Armengaud
Journal:  J Biol Chem       Date:  2010-10-26       Impact factor: 5.157

2.  Systematic Evaluation of Protein Reduction and Alkylation Reveals Massive Unspecific Side Effects by Iodine-containing Reagents.

Authors:  Torsten Müller; Dominic Winter
Journal:  Mol Cell Proteomics       Date:  2017-05-24       Impact factor: 5.911

Review 3.  Oxidative protein labeling in mass-spectrometry-based proteomics.

Authors:  Julien Roeser; Rainer Bischoff; Andries P Bruins; Hjalmar P Permentier
Journal:  Anal Bioanal Chem       Date:  2010-02-13       Impact factor: 4.142

  3 in total

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