Biomedical and Organic Chemistry Department, Laboratoire National de Métrologie et d'Essais (LNE), Paris, France.
Biological Mass Spectrometry and Proteomics, SMBP, ESPCI Paris, Université PSL, CNRS FRE2032, Paris, France.
Anal Bioanal Chem. 2021 Aug;413(19):4707-4725. doi: 10.1007/s00216-021-03361-0. Epub 2021 May 14.
The quantification of low abundant proteins in complex matrices by liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) remains challenging. A measurement procedure based on optimized antibody-free sample preparation and isotope dilution coupled to LC-MS/MS was developed to quantify procalcitonin (PCT) in human serum at sub-microgram per liter level. A combination of sodium deoxycholate-assisted protein precipitation with acetonitrile, solid-phase extraction, and trypsin digestion assisted with Tween-20 enhanced the method sensitivity. Linearity was established through peptide-based calibration curves in the serum matrix (0.092-5.222 μg/L of PCT) with a good linear fit (R2 ≥ 0.999). Quality control materials spiked with known amounts of protein-based standards were used to evaluate the method's accuracy. The bias ranged from -2.6 to +4.3%, and the intra-day and inter-day coefficients of variations (CVs) were below 2.2% for peptide-based quality controls. A well-characterized correction factor was determined and applied to compensate for digestion incompleteness and material loss before the internal standards spike. Results with metrological traceability to the SI units were established using standard peptide of well-characterized purity determined by peptide impurity corrected amino acid analysis. The validated method enables accurate quantification of PCT in human serum at a limit of quantification down to 0.245 μg/L (bias -1.9%, precision 9.1%). The method was successfully applied to serum samples obtained from patients with sepsis. Interestingly, the PCT concentration reported implementing the isotope dilution LC-MS/MS method was twofold lower than the concentration provided by an immunoassay.
在复杂基质中通过液相色谱与串联质谱(LC-MS/MS)对低丰度蛋白质进行定量仍然具有挑战性。本研究开发了一种基于优化抗体自由样品制备和同位素稀释与 LC-MS/MS 耦联的测量程序,以亚微克/升水平定量人血清中的降钙素原(PCT)。联合使用去氧胆酸钠辅助的蛋白质沉淀与乙腈、固相萃取和含有吐温-20 的胰蛋白酶消化,增强了方法的灵敏度。通过在血清基质中基于肽的校准曲线(PCT 为 0.092-5.222μg/L)建立了线性关系,具有良好的线性拟合(R2≥0.999)。使用含有已知量蛋白质标准品的质控材料来评估方法的准确性。基于肽的质控的偏差范围为-2.6%至+4.3%,日内和日间变异系数(CV)低于 2.2%。确定了一个特征良好的校正因子,用于补偿内标物添加前消化不完全和物质损失。通过使用经肽杂质校正的氨基酸分析确定的具有良好特征纯度的标准肽建立了与 SI 单位具有计量溯源性的结果。该经过验证的方法能够准确地定量人血清中的 PCT,定量下限低至 0.245μg/L(偏差-1.9%,精密度 9.1%)。该方法成功地应用于脓毒症患者的血清样本。有趣的是,报告的实施同位素稀释 LC-MS/MS 方法的 PCT 浓度比免疫测定提供的浓度低两倍。