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

被引:24
作者
Bailey, Ulla-Maja [1 ]
Punyadeera, Chamindie [2 ,3 ]
Cooper-White, Justin J. [2 ,3 ]
Schulz, Benjamin L. [1 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Saliva Translat Res Grp, Tissue Engn & Microfluid Lab, Brisbane, Qld 4072, Australia
[3] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2012年 / 911卷
基金
澳大利亚国家健康与医学研究理事会;
关键词
Saliva; Alpha-amylase; Liquid chromatography; Mass spectrometry; Proteolysis; Biomarker; PROTEINS; IDENTIFICATION; PROFILES; TANNIN; FORMS;
D O I
10.1016/j.jchromb.2012.10.023
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:21 / 26
页数:6
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