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基于芯片的反相液相色谱-质谱联用技术分析全甲基化 N-连接糖肽:一种用于癌症生物标志物发现的潜在方法。

Chip-based reversed-phase liquid chromatography-mass spectrometry of permethylated N-linked glycans: a potential methodology for cancer-biomarker discovery.

机构信息

National Center for Glycomics and Glycoproteomics, Indiana University, Bloomington, Indiana 47405, USA.

出版信息

Anal Chem. 2010 Jun 15;82(12):5095-106. doi: 10.1021/ac100131e.

Abstract

The study of protein glycosylation in biological fluids and tissues has substantial medical importance, as changes in glycan structures have now been associated with a number of diseases. Quantification of glycomic-profile changes is becoming increasingly important in the search for disease biomarkers. Here, we report a highly reproducible combination of a glycomic sample preparation/solid-phase derivatization of glycoprotein-derived N-linked glycans with their subsequent microchip-based separation and mass-spectrometric (MS) measurements. Following our previously described reductive beta-elimination for O-linked glycans with ammonia-borane complex to reduce N-linked structures, the N-linked alditol structures are effectively methylated in dimethylformamide medium to avoid artefacts in MS measurements. Reversed-phase microfluidic liquid chromatography (LC) of methylated N-linked oligosaccharide alditols resolved some closely related structures into regular retention increments, aiding in their structural assignments. Optimized LC gradients, together with nanospray MS, have been applied here in the quantitative measurements of N-linked glycans in blood serum, distinguishing breast cancer patients from control individuals.

摘要

在生物体液和组织中研究蛋白质糖基化具有重要的医学意义,因为糖链结构的变化现在与许多疾病有关。糖组图谱变化的定量分析在寻找疾病生物标志物方面变得越来越重要。在这里,我们报告了一种高度可重复的组合,即糖基化样品制备/固相衍生糖蛋白衍生的 N-连接聚糖,以及随后的基于微芯片的分离和质谱(MS)测量。在我们之前描述的用氨硼烷复合物对 O-连接聚糖进行还原 β-消除以还原 N-连接结构之后,N-连接糖醇结构在二甲基甲酰胺介质中有效地甲基化,以避免 MS 测量中的假象。经还原 β-消除处理后的 N-连接寡糖醛糖醇的反相微流控液相色谱(LC)将一些密切相关的结构分离成常规保留增量,有助于它们的结构分配。优化的 LC 梯度,与纳喷雾 MS 一起,已应用于血清中 N-连接聚糖的定量测量,将乳腺癌患者与对照个体区分开来。

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