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使用高度多重反应监测质谱法测定来自21批商业人血浆的267种蛋白质的浓度范围。

Determination of the concentration range for 267 proteins from 21 lots of commercial human plasma using highly multiplexed multiple reaction monitoring mass spectrometry.

作者信息

Gaither Claudia, Popp Robert, Mohammed Yassene, Borchers Christoph H

机构信息

MRM Proteomics Inc., 141 Avenue du Président-Kennedy, SB-5100, C.P. #26, Montreal, QC H2X 3X8, Canada.

University of Victoria - Genome British Columbia Proteomics Centre, University of Victoria, Victoria, British Columbia V8Z 7X8, Canada and Center for Proteomics and Metabolomics, Leiden University Medical Center, Albinusdreef 2, Leiden, 2333 ZA, The Netherlands.

出版信息

Analyst. 2020 May 18;145(10):3634-3644. doi: 10.1039/c9an01893j.

Abstract

Multiple reaction monitoring (MRM) is a key tool for biomarker validation and the translation of potential biomarkers into the clinic. To demonstrate the applicability of MRM towards achieving this goal, we set out to determine the concentration ranges of 267 plasma proteins, including 61 FDA-approved/LDT developed biomarkers, in 21 commercial human plasma lots, as well as to assess accuracy and precision. Each target protein was quantified by calculating the area ratio of the endogenous tryptic target peptide to its stable isotope-labelled internal standard equivalent and compared to a standard curve. This highly multiplexed approach utilized a standard-flow UHPLC system linked to a triple quadrupole. All samples were analyzed across three separate days and assessed for robustness and accuracy. The standard curves and quality control samples showed excellent performance, with >93% of standards and QCs meeting the acceptance criteria. A total of 248 proteins were able to be quantified in at least one sample on at least one of the three days, with 111 proteins being quantified in all 21 samples on all three days. The protein concentrations across all proteins covered six orders of magnitude. Furthermore, excellent three-day precision was demonstrated with 86% of CVs falling below 15%. Overall, the protein concentration differences ranged from 1.1-fold for metalloproteinase inhibitor 2, to 69-fold for serum amyloid A-1/A-2.

摘要

多反应监测(MRM)是生物标志物验证以及将潜在生物标志物转化应用于临床的关键工具。为证明MRM在实现这一目标方面的适用性,我们着手测定21个市售人血浆批次中267种血浆蛋白的浓度范围,其中包括61种经美国食品药品监督管理局(FDA)批准/通过实验室开发检测方法(LDT)开发的生物标志物,并评估其准确性和精密度。通过计算内源性胰蛋白酶作用的目标肽与其稳定同位素标记的内标等效物的面积比来对每种目标蛋白进行定量,并与标准曲线进行比较。这种高度多重化的方法采用了与三重四极杆相连的标准流速超高效液相色谱(UHPLC)系统。所有样品在三个不同日期进行分析,并评估其稳健性和准确性。标准曲线和质量控制样品表现出色,超过93%的标准品和质控品符合验收标准。在三天中的至少一天,至少有一个样品中能够对总共248种蛋白质进行定量,其中111种蛋白质在所有三天的所有21个样品中均能被定量。所有蛋白质的浓度范围跨越六个数量级。此外,还证明了出色的三天精密度,86%的变异系数(CV)低于15%。总体而言,蛋白质浓度差异范围从金属蛋白酶抑制剂2的1.1倍到血清淀粉样蛋白A-1/A-2的69倍。

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