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ABSTRACT: Background
Absolute quantification of protein biomarkers such as serum apolipoprotein A1 by both immunoassays and LC-MS can provide misleading results.Results
Recombinant ApoA-1 internal standard was prepared using stable isotope labeling by amino acids in cell culture with [(13)C6(15)N2]-lysine and [(13)C9(15)N1]-tyrosine in human cells. A stable isotope dilution LC-MS method for serum ApoA-1 was validated and levels analyzed for 50 nonsmokers and 50 smokers.Conclusion
The concentration of ApoA-1 in nonsmokers was 169.4 mg/dl with an 18.4% reduction to 138.2 mg/dl in smokers. The validated assay will have clinical utility for assessing effects of smoking cessation and therapeutic or dietary interventions in high-risk populations.
SUBMITTER: Wang Q
PROVIDER: S-EPMC4737526 | biostudies-literature | 2015
REPOSITORIES: biostudies-literature
Wang Qingqing Q Zhang Suhong S Guo Lili L Busch Christine M CM Jian Wenying W Weng Naidong N Snyder Nathaniel W NW Rangiah Kannan K Mesaros Clementina C Blair Ian A IA
Bioanalysis 20150922 22
<h4>Background</h4>Absolute quantification of protein biomarkers such as serum apolipoprotein A1 by both immunoassays and LC-MS can provide misleading results.<h4>Results</h4>Recombinant ApoA-1 internal standard was prepared using stable isotope labeling by amino acids in cell culture with [(13)C6(15)N2]-lysine and [(13)C9(15)N1]-tyrosine in human cells. A stable isotope dilution LC-MS method for serum ApoA-1 was validated and levels analyzed for 50 nonsmokers and 50 smokers.<h4>Conclusion</h4>T ...[more]