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用于分析肝素寡糖和低分子量肝素的毛细管电泳-质谱法

Capillary Electrophoresis-Mass Spectrometry for the Analysis of Heparin Oligosaccharides and Low Molecular Weight Heparin.

作者信息

Sun Xiaojun, Lin Lei, Liu Xinyue, Zhang Fuming, Chi Lianli, Xia Qiangwei, Linhardt Robert J

机构信息

National Glycoengineering Research Center, Shandong University , Jinan 250100, China.

CMP Scientific, Corporation, 760 Parkside Avenue, Brooklyn, New York 11226, United States.

出版信息

Anal Chem. 2016 Feb 2;88(3):1937-43. doi: 10.1021/acs.analchem.5b04405. Epub 2016 Jan 13.

Abstract

Heparins, highly sulfated, linear polysaccharides also known as glycosaminoglycans, are among the most challenging biopolymers to analyze. Hyphenated techniques in conjunction with mass spectrometry (MS) offer rapid analysis of complex glycosaminoglycan mixtures, providing detailed structural and quantitative data. Previous analytical approaches have often relied on liquid chromatography (LC)-MS, and some have limitations including long separation times, low resolution of oligosaccharide mixtures, incompatibility of eluents, and often require oligosaccharide derivatization. This study examines the analysis of glycosaminoglycan oligosaccharides using a novel electrokinetic pump-based capillary electrophoresis (CE)-MS interface. CE separation and electrospray were optimized using a volatile ammonium bicarbonate electrolyte and a methanol-formic acid sheath fluid. The online analyses of highly sulfated heparin oligosaccharides, ranging from disaccharides to low molecular weight heparins, were performed within a 10 min time frame, offering an opportunity for higher-throughput analysis. Disaccharide compositional analysis as well as top-down analysis of low molecular weight heparin was demonstrated. Using normal polarity CE separation and positive-ion electrospray ionization MS, excellent run-to-run reproducibility (relative standard deviation of 3.6-5.1% for peak area and 0.2-0.4% for peak migration time) and sensitivity (limit of quantification of 2.0-5.9 ng/mL and limit of detection of 0.6-1.8 ng/mL) could be achieved.

摘要

肝素是一种高度硫酸化的线性多糖,也被称为糖胺聚糖,是最难分析的生物聚合物之一。联用技术与质谱(MS)相结合,可对复杂的糖胺聚糖混合物进行快速分析,提供详细的结构和定量数据。以往的分析方法通常依赖于液相色谱(LC)-MS,其中一些方法存在局限性,包括分离时间长、寡糖混合物分辨率低、洗脱液不兼容,且通常需要对寡糖进行衍生化。本研究考察了使用一种基于新型电动泵的毛细管电泳(CE)-MS接口对糖胺聚糖寡糖进行分析的情况。使用挥发性碳酸氢铵电解质和甲醇-甲酸鞘液对CE分离和电喷雾进行了优化。在10分钟的时间范围内对从二糖到低分子量肝素的高度硫酸化肝素寡糖进行了在线分析,为高通量分析提供了机会。展示了二糖组成分析以及低分子量肝素的自上而下分析。使用正相CE分离和正离子电喷雾电离MS,可实现出色的批间重现性(峰面积的相对标准偏差为3.6-5.1%,峰迁移时间的相对标准偏差为0.2-0.4%)和灵敏度(定量限为2.0-5.9 ng/mL,检测限为0.6-1.8 ng/mL)。

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