Analysis of Keratan Sulfate Oligosaccharides by Electrospray Ionization Tandem Mass Spectrometry

Yuntao Zhang,* Yutaka Kariya, Abigail H. Conrad, Elena S. Tasheva, and Gary W. Conrad
Division of Biology, Kansas State University, Manhattan, Kansas 66506, and Central Research Laboratories, Seikagaku Corporation, Higashiyamato-shi, Tokyo 207-0021, Japan
Anal. Chem., 2005, 77 (3), pp 902–910
DOI: 10.1021/ac040074j
Publication Date (Web): January 4, 2005
Copyright © 2005 American Chemical Society
*

 Corresponding author. Tel:  785-532-6553. Fax:  785-532-6653. E-mail:  ytz@ksu.edu.

,

 Kansas State University.

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 Seikagaku Corp.

Abstract

Keratan sulfate (KS) is a glycosaminoglycan consisting of repeating disaccharide units composed of alternating residues of d-galactose and N-acetyl-d-glucosamine linked β-(1−4) and β-(1−3), respectively. In this study, electrospray ionization tandem mass spectrometry (ESI-MS/MS) was employed to identify keratan sulfate oligosaccharides. Two nonsulfated disaccharide isomers and two monosulfated disaccharide isomers were distinguished through MS/MS. In MS1 spectra of multiply sulfated KS oligosaccharides, the charge state of the most abundant molecular ion equals the number of sulfates. Subsequent MS2 and MS3 spectra of mono-, di-, tri-, and tetrasulfated KS oligosaccharides and sialylated tetrasaccharides reveal diagnostic ions that can be used as fingerprint maps to identify unknown KS oligosaccharides. Based on the pattern of fragment ions, the compositions of an oligosaccharide mixture from shark cartilage KS and of two enzyme digests of bovine corneal KS were determined directly, without prior isolation of individual oligosaccharides by HPLC or other methods.

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History

  • Published In Issue February 01, 2005
  • Received for review April 23, 2004. Accepted November 10, 2004.

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