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靶向在线 SPE-LC-MS/MS 法测定人血中的 12 种载脂蛋白

Targeted On-line SPE-LC-MS/MS Assay for the Quantitation of 12 Apolipoproteins from Human Blood.

机构信息

Institute of Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University Hospital Leipzig, Leipzig, Germany.

LIFE, Leipzig Research Center for Civilization Diseases, Leipzig University, Leipzig, Germany.

出版信息

Proteomics. 2018 Feb;18(3-4). doi: 10.1002/pmic.201700279. Epub 2018 Feb 2.

DOI:10.1002/pmic.201700279
PMID:29280342
Abstract

Laborious sample pretreatment of biological samples represents the most limiting factor for the translation of targeted proteomics assays from research to clinical routine. An optimized method for the simultaneous quantitation of 12 major apolipoproteins (apos) combining on-line SPE and fast LC-MS/MS analysis in 6.5 min total run time was developed, reducing the manual sample pretreatment time of 3 μL serum or plasma by 60%. Within-run and between-day imprecisions below 10 and 15% (n = 10) and high recovery rates (94-131%) were obtained applying the high-throughput setup. High-quality porcine trypsin was used, which outperformed cost-effective bovine trypsin regarding digestion efficiency. Comparisons with immunoassays and another LC-MS/MS assay demonstrated good correlation (Pearson's R: 0.81-0.98). Further, requirements on sample quality concerning sampling, processing, and long-term storage up to 1 year were investigated revealing significant influences of the applied sampling material and coagulant on quantitation results. Apo profiles of 1339 subjects of the LIFE-Adult-Study were associated with lifestyle and physiological parameters as well as establish parameters of lipid metabolism (e.g., triglycerides, cholesterol). Besides gender effects, most significant impact was seen regarding lipid-lowering medication. In conclusion, this novel highly standardized, high-throughput targeted proteomics assay utilizes a fast, simultaneous analysis of 12 apos from least sample amounts.

摘要

生物样本的费力样品预处理是将靶向蛋白质组学测定从研究转化为临床常规的最具限制性因素。本研究开发了一种优化的方法,用于结合在线 SPE 和快速 LC-MS/MS 分析,在 6.5 分钟的总运行时间内同时定量 12 种主要载脂蛋白 (apos),将 3μL 血清或血浆的手动样品预处理时间减少了 60%。通过高通量设置获得了低于 10%和 15%(n=10)的日内和日间精密度以及高回收率(94-131%)。应用了高质量的猪胰蛋白酶,其消化效率优于具有成本效益的牛胰蛋白酶。与免疫测定和另一种 LC-MS/MS 测定的比较表明具有良好的相关性(Pearson's R:0.81-0.98)。此外,还研究了关于采样、处理和长达 1 年的长期储存的样品质量要求,结果表明应用的采样材料和凝固剂对定量结果有显著影响。LIFE-Adult-Study 中 1339 名受试者的 apo 谱与生活方式和生理参数以及脂质代谢参数(如甘油三酯、胆固醇)相关。除了性别影响外,降脂药物的影响最为显著。总之,这种新型高度标准化、高通量的靶向蛋白质组学测定方法利用最少的样品量进行快速、同时分析 12 种 apo。

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