کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7634143 | 1494731 | 2017 | 30 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
On-column trypsin digestion coupled with LC-MS/MS for quantification of apolipoproteins
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موضوعات مرتبط
مهندسی و علوم پایه
شیمی
شیمی آنالیزی یا شیمی تجزیه
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چکیده انگلیسی
Apolipoproteins are potential biomarkers for assessing metabolic irregularities that are associated with the development of cardiovascular disease (CVD). Quantitative measurement of apolipoproteins in serum or plasma by LC-IDMS allows the analysis of numerous proteins in the same sample run. However, the accuracy and precision of the IDMS measurement depends on the reproducibility of the enzymatic protein digestion step. With the application of an immobilized enzyme reactor (IMER), the reproducibility of the trypsin digestion can be controlled with high precision via flow rate, column volume and temperature. In this report, we demonstrate the application of an integrated IMER-LC-MS/MS platform for the simultaneous quantitative analysis of eight different apolipoproteins. Using a dilution series of a characterized serum pool as calibrator, the method was validated by repeated analysis of pooled sera and individual serum samples with a wide range of lipid profiles, all showing intra-assay CVÂ <Â 4.4% and inter-assay CVÂ <Â 8%. In addition, the method was compared with traditional homogeneous digestion coupled IDMS for the quantification of apoA-I and apoB-100. Applied in large scale human population studies, this method can serve the translation of a wider panel of apolipoprotein biomarkers from research to clinical application.217
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Proteomics - Volume 150, 6 January 2017, Pages 258-267
Journal: Journal of Proteomics - Volume 150, 6 January 2017, Pages 258-267
نویسندگان
Christopher A Toth, Zsuzsanna Kuklenyik, Jeffrey I Jones, Bryan A Parks, Michael S Gardner, David M Schieltz, Jon C Rees, Michael L Andrews, Lisa G McWilliams, James L Pirkle, John R Barr,