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


Autoria(s): Bailey, Ulla-Maja; Punyadeera, Chamindie; Cooper-White, Justin J.; Schulz, Benjamin L.
Data(s)

12/12/2012

Resumo

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. (C) 2012 Elsevier B.V. All rights reserved.

Identificador

http://eprints.qut.edu.au/77926/

Publicador

Elsevier BV

Relação

DOI:10.1016/j.jchromb.2012.10.023

Bailey, Ulla-Maja, Punyadeera, Chamindie, Cooper-White, Justin J., & Schulz, Benjamin L. (2012) Analysis of the extreme diversity of salivary alpha-amylase isoforms generated by physiological proteolysis using liquid chromatography-tandem mass spectrometry. Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, 911, pp. 21-26.

Direitos

Copyright 2012 Elsevier BV

Fonte

School of Biomedical Sciences; Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #Saliva #Alpha-amylase #Liquid chromatography #Mass spectrometry #Proteolysis #Biomarker #proteins #identification #profiles #binding #tannin #forms
Tipo

Journal Article