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用于分析硫酸软骨素和硫酸皮肤素衍生二糖的毛细管电泳

Capillary electrophoresis for the analysis of chondroitin sulfate- and dermatan sulfate-derived disaccharides.

作者信息

al-Hakim A, Linhardt R J

机构信息

Division of Medicinal and Natural Products Chemistry, College of Pharmacy, University of Iowa, Iowa City 52242.

出版信息

Anal Biochem. 1991 May 15;195(1):68-73. doi: 10.1016/0003-2697(91)90296-6.

Abstract

High-voltage capillary zone electrophoresis (CZE) has been used for the first time in the analysis of non-, mono-, di-, and trisulfated disaccharides derived from chondroitin sulfate, dermatan sulfate, and hyaluronic acid. These glycosaminoglycans are first depolymerized using polysaccharide lyases. The resulting unsaturated disaccharide products can be detected by their ultraviolet absorbance at 232 nm. Different retention times were obtained for each unsaturated disaccharide analyzed by CZE. The application of a constant voltage across a 70-cm fused silica capillary using a single, simple buffer system resolved an eight-component mixture within 40 min. Quantitation of disaccharides derived from chondroitin sulfate using chondroitin ABC lyase (EC 4.2.2.4) and mixtures of unsaturated disaccharide standards was possible requiring only picogram quantities of sample. The disaccharides examined had a net charge of from -1 to -4 and were resolved primarily on the basis of net charge and secondarily on the basis of charge distribution. Two unsulfated disaccharides both containing the same unsaturated uronic acid residue were analyzed. One was from chondroitin having an N-acetylgalactosyl residue and one from hyaluronate having an N-acetylglycosyl residue. Despite the fact that they differed only by the chirality at one center, these disaccharides were resolved by CZE. CZE is a fast and simple method that represents a powerful new tool for analysis and separation of acidic disaccharide components of glycosaminoglycans.

摘要

高压毛细管区带电泳(CZE)首次用于分析硫酸软骨素、硫酸皮肤素和透明质酸衍生的非硫酸化、单硫酸化、二硫酸化和三硫酸化二糖。这些糖胺聚糖首先使用多糖裂解酶进行解聚。所得不饱和二糖产物可通过其在232nm处的紫外吸光度进行检测。通过CZE分析的每种不饱和二糖获得了不同的保留时间。使用单一、简单的缓冲系统在70cm的熔融石英毛细管上施加恒定电压,可在40分钟内分离出八组分混合物。使用硫酸软骨素ABC裂解酶(EC 4.2.2.4)和不饱和二糖标准品混合物对硫酸软骨素衍生的二糖进行定量分析,仅需皮克量的样品。所检测的二糖净电荷为-1至-4,主要根据净电荷进行分离,其次根据电荷分布进行分离。分析了两种均含有相同不饱和糖醛酸残基的非硫酸化二糖。一种来自具有N-乙酰半乳糖基残基的软骨素,另一种来自具有N-乙酰糖基残基的透明质酸。尽管它们仅在一个中心的手性上有所不同,但这些二糖通过CZE得以分离。CZE是一种快速且简单的方法,是分析和分离糖胺聚糖酸性二糖成分的强大新工具。

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