Antibody-free LC-HRMS/MS method for simultaneous quantification of NGAL, CRP and SAA in serum from sepsis patients

IF 2.8 2区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of proteomics Pub Date : 2025-02-01 DOI:10.1016/j.jprot.2025.105396
Maxence Derbez-Morin , Vincent Delatour , François Fenaille , Catherine Perrot , Anne-Marie Dupuy , Amandine Boeuf , François Becher
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Abstract

Liquid chromatography coupled with high-resolution mass spectrometry (LC-HRMS/MS) is a valuable alternative to ligand-binding assay, enabling specific and accurate quantification of protein biomarkers. We developed a robust antibody-free LC-HRMS/MS method for the multiplex quantification of three sepsis biomarkers in serum: NGAL, CRP and SAA. The method was thoroughly optimized from sample preparation to LC-HRMS/MS analysis, alongside the calibration. Specifically, a modified trichloroacetic acid/isopropanol protein precipitation procedure combined with an optimized Parallel Reaction Monitoring acquisition allowed the quantification of the low abundant NGAL at ng/mL levels. While reference material and reference measurement procedure were available for CRP, no such standards existed for NGAL and SAA. Well-characterized peptide calibrators traceable to the international system of units were developed for NGAL and SAA. The method demonstrated suitable trueness and precision for the quantification of NGAL, CRP, and SAA with coefficients of variation (CV%) ranging from 1.6 % to 22.4 % and bias between −12.6 % and +18.0 %. Successful application to pooled serum samples illustrated the method's effectiveness. Our results pave the way toward the development of reference systems for additional sepsis biomarkers.

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无抗体LC-HRMS/MS法同时定量脓毒症患者血清中NGAL、CRP和SAA。
液相色谱联用高分辨率质谱(LC-HRMS/MS)是一种有价值的替代配体结合测定的方法,可以实现特异性和准确的蛋白质生物标志物定量。我们开发了一种强大的无抗体LC-HRMS/MS方法,用于多重定量血清中三种败血症生物标志物:NGAL, CRP和SAA。从样品制备到LC-HRMS/MS分析,以及校准,对该方法进行了全面优化。具体来说,改进的三氯乙酸/异丙醇蛋白沉淀程序结合优化的平行反应监测采集允许在ng/mL水平上定量低丰度的NGAL。CRP有参考物质和参考测量方法,而NGAL和SAA没有这样的标准。为NGAL和SAA开发了表征良好的肽校准器,可追溯至国际单位制。该方法对NGAL、CRP和SAA的定量具有较好的准确性和精密度,变异系数(CV%)范围为1.6 % ~ 22.4 %,偏差范围为-12.6 % ~ +18.0 %。该方法在混合血清样品中的成功应用说明了该方法的有效性。我们的结果为开发其他败血症生物标志物的参考系统铺平了道路。
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来源期刊
Journal of proteomics
Journal of proteomics 生物-生化研究方法
CiteScore
7.10
自引率
3.00%
发文量
227
审稿时长
73 days
期刊介绍: Journal of Proteomics is aimed at protein scientists and analytical chemists in the field of proteomics, biomarker discovery, protein analytics, plant proteomics, microbial and animal proteomics, human studies, tissue imaging by mass spectrometry, non-conventional and non-model organism proteomics, and protein bioinformatics. The journal welcomes papers in new and upcoming areas such as metabolomics, genomics, systems biology, toxicogenomics, pharmacoproteomics. Journal of Proteomics unifies both fundamental scientists and clinicians, and includes translational research. Suggestions for reviews, webinars and thematic issues are welcome.
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