• Title of article

    Analysis of the extreme diversity of salivary alpha-amylase isoforms generated by physiological proteolysis using liquid chromatography–tandem mass spectrometry

  • Author/Authors

    Bailey، نويسنده , , Ulla-Maja and Punyadeera، نويسنده , , Chamindie and Cooper-White، نويسنده , , Justin J. and Schulz، نويسنده , , Benjamin L.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2012
  • Pages
    6
  • From page
    21
  • To page
    26
  • Abstract
    Saliva is a crucial biofluid for oral health and is also of increasing importance as a non-invasive source of disease biomarkers. Salivary alpha-amylase is an abundant protein in saliva, and changes in amylase expression have been previously associated with a variety of diseases and conditions. Salivary alpha-amylase is subject to a high diversity of post-translational modifications, including physiological proteolysis in the oral cavity. Here we developed methodology for rapid sample preparation and non-targeted LC–ESI-MS/MS analysis of saliva from healthy subjects and observed an extreme diversity of alpha-amylase proteolytic isoforms. Our results emphasize the importance of consideration of post-translational events such as proteolysis in proteomic studies, biomarker discovery and validation, particularly in saliva.
  • Keywords
    mass spectrometry , Biomarker , Saliva , alpha-amylase , Liquid chromatography , Proteolysis
  • Journal title
    Journal of Chromatography B
  • Serial Year
    2012
  • Journal title
    Journal of Chromatography B
  • Record number

    1470697