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多孔石墨化碳纳米液相色谱-质谱法进行全面糖基分析。

Comprehensive -Glycan Analysis by Porous Graphitized Carbon Nanoliquid Chromatography-Mass Spectrometry.

机构信息

Center for Proteomics and Metabolomics, Leiden University Medical Center, P.O. Box 9600, Leiden 2300 RC, The Netherlands.

出版信息

Anal Chem. 2024 Jun 4;96(22):8942-8948. doi: 10.1021/acs.analchem.3c05826. Epub 2024 May 17.

Abstract

The diverse and unpredictable structures of -GalNAc-type protein glycosylation present a challenge for its structural and functional characterization in a biological system. Porous graphitized carbon (PGC) liquid chromatography (LC) coupled to mass spectrometry (MS) has become one of the most powerful methods for the global analysis of glycans in complex biological samples, mainly due to the extensive chromatographic separation of (isomeric) glycan structures and the information delivered by collision induced fragmentation in negative mode MS for structural elucidation. However, current PGC-based methodologies fail to detect the smaller glycan species consisting of one or two monosaccharides, such as the Tn (single GalNAc) antigen, which is broadly implicated in cancer biology. This limitation is caused by the loss of small saccharides during sample preparation and LC. Here, we improved the conventional PGC nano-LC-MS/MS-based strategy for -glycan analysis, enabling the detection of truncated -glycan species and improving isomer separation. This was achieved by the implementation of 2.7 μm PGC particles in both the trap and analytical LC columns, which provided an enhanced binding capacity and isomer separation for -glycans. Furthermore, a novel mixed-mode PGC-boronic acid-solid phase extraction during sample preparation was established to purify a broad range of glycans in an unbiased manner, including the previously missed mono- and disaccharides. Taken together, the optimized PGC nano-LC-MS/MS platform presents a powerful component of the toolbox for comprehensive -glycan characterization.

摘要
  • GalNAc 型蛋白糖基化的结构多样且不可预测,这给其在生物系统中的结构和功能表征带来了挑战。多孔石墨化碳(PGC)液相色谱(LC)与质谱(MS)联用已成为分析复杂生物样品中聚糖的最有力方法之一,这主要归因于(异构)聚糖结构的广泛色谱分离以及在负模式 MS 中碰撞诱导碎裂提供的结构解析信息。然而,目前基于 PGC 的方法无法检测到由一个或两个单糖组成的较小聚糖种类,例如 Tn(单 GalNAc)抗原,它广泛涉及癌症生物学。这种局限性是由于样品制备和 LC 过程中损失了小糖。在这里,我们改进了基于常规 PGC 纳升 LC-MS/MS 的 - 聚糖分析策略,能够检测到截断的 - 聚糖种类并改善异构体分离。这是通过在捕集和分析 LC 柱中都使用 2.7 μm PGC 颗粒来实现的,这为 - 聚糖提供了增强的结合能力和异构体分离。此外,在样品制备过程中建立了一种新的混合模式 PGC-硼酸固相萃取,以无偏倚的方式纯化广泛的聚糖,包括之前错过的单糖和二糖。总之,优化后的 PGC 纳升 LC-MS/MS 平台为全面的 - 聚糖表征提供了一个强大的工具包组件。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9b2/11154684/a43ae752fc4e/ac3c05826_0001.jpg

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