Analysis of Glycosaminoglycans Using Mass Spectrometry

被引:1
作者
Staples, Gregory O. [1 ]
Zaia, Joseph [1 ]
机构
[1] Boston Univ, Sch Med, Ctr Biomed Mass Spectrometry, Dept Biochem, 670 Albany St,Rm 509, Boston, MA 02118 USA
关键词
Chondroitin sulfate; dermatan sulfate; glycosaminoglycan; heparan sulfate; heparin; proteoglycan; hyaluronan; keratan sulfate; mass spectrometry; PERFORMANCE LIQUID-CHROMATOGRAPHY; CHONDROITIN SULFATE OLIGOSACCHARIDES; HEPARIN-LIKE GLYCOSAMINOGLYCANS; TIME-OF-FLIGHT; ELECTRON DETACHMENT DISSOCIATION; IONIZATION-QUADRUPOLE TIME; HYDROPHILIC-INTERACTION CHROMATOGRAPHY; GRAPHITIZED CARBON COLUMN; MOLECULAR-WEIGHT HEPARIN; III BINDING-SITE;
D O I
暂无
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The glycosaminoglycans (GAGs) are linear polysaccharides expressed on animal cell surfaces and in extracellular matrices. Their biosynthesis is under complex control and confers a domain structure that is essential to their ability to bind to protein partners. Key to understanding the functions of GAGs are methods to determine accurately and rapidly patterns of sulfation, acetylation and uronic acid epimerization that correlate with protein binding or other biological activities. Mass spectrometry (MS) is particularly suitable for the analysis of GAGs for biomedical purposes. Using modern ionization techniques it is possible to accurately determine molecular weights of GAG oligosaccharides and their distributions within a mixture. Methods for direct interfacing with liquid chromatography have been developed to permit on-line mass spectrometric analysis of GAGs. New tandem mass spectrometric methods for fine structure determination of GAGs are emerging. This review summarizes MS-based approaches for analysis of GAGs, including tissue extraction and chromatographic methods compatible with LC/MS and tandem MS.
引用
收藏
页码:325 / 336
页数:12
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