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人生物流体中高通量糖胺聚糖提取及超高效液相色谱-串联质谱定量分析

High-throughput glycosaminoglycan extraction and UHPLC-MS/MS quantification in human biofluids.

作者信息

Volpi Nicola, Galeotti Fabio, Gatto Francesco

机构信息

Department of Life Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Department of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.

出版信息

Nat Protoc. 2025 Apr;20(4):843-860. doi: 10.1038/s41596-024-01078-9. Epub 2024 Nov 14.

DOI:10.1038/s41596-024-01078-9
PMID:39543382
Abstract

Glycosaminoglycans (GAGs) are linear, unbranched heteropolysaccharides whose structural complexity determines their function. Accurate quantification of GAGs in biofluids at high throughput is relevant for numerous biomedical applications. However, because of the structural variability of GAGs in biofluids, existing protocols require complex pre-analytical procedures, have limited throughput and lack accuracy. Here, we describe the extraction and quantification of GAGs by using ultra-high-performance liquid chromatography coupled with triple-quadrupole mass spectrometry (UHPLC-MS/MS). Designed for 96-well plates, this method enables the processing of up to 82 study samples per plate, with the remaining 14 wells used for calibrators and controls. Key steps include the enzymatic depolymerization of GAGs, their derivatization with 2-aminoacridone and their quantification via UHPLC-MS/MS. Each plate can be analyzed in a single UHPLC-MS/MS run, offering the quantitative and scalable analysis of 17 disaccharides from chondroitin sulfate, heparan sulfate and hyaluronic acid, with a level of precision and reproducibility sufficient for their use as biomarkers. The procedure from sample thawing to initiating the UHPLC-MS/MS run can be completed in ~1.5 d plus 15 min of MS runtime per sample, and it is structured to fit within ordinary working shifts, thus making it a valuable tool for clinical laboratories seeking high-throughput analysis of GAGs. The protocol requires expertise in UHPLC-MS/MS.

摘要

糖胺聚糖(GAGs)是线性、无分支的杂多糖,其结构复杂性决定了它们的功能。对生物流体中的GAGs进行高通量的准确定量在众多生物医学应用中具有重要意义。然而,由于生物流体中GAGs的结构变异性,现有方案需要复杂的分析前程序,通量有限且缺乏准确性。在此,我们描述了使用超高效液相色谱与三重四极杆质谱联用(UHPLC-MS/MS)对GAGs进行提取和定量的方法。该方法专为96孔板设计,每板最多可处理82个研究样本,其余14孔用于校准物和对照。关键步骤包括GAGs的酶促解聚、用2-氨基吖啶进行衍生化以及通过UHPLC-MS/MS进行定量。每个板可在一次UHPLC-MS/MS运行中进行分析,可对来自硫酸软骨素、硫酸乙酰肝素和透明质酸的17种二糖进行定量和可扩展分析,其精密度和重现性水平足以用作生物标志物。从样品解冻到启动UHPLC-MS/MS运行的过程可在约1.5天内完成,每个样品还需15分钟的质谱运行时间,并且其流程安排适合正常工作班次,因此对于寻求对GAGs进行高通量分析的临床实验室而言,它是一种有价值的工具。该方案需要UHPLC-MS/MS方面的专业知识。

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