Analysis of Total N-Glycans in Cell Membrane Fractions of Cancer Cells Using a Combination of Serotonin Affinity Chromatography and Normal Phase Chromatography

Ryosuke Naka, Satoru Kamoda, Aya Ishizuka, Mitsuhiro Kinoshita, and Kazuaki Kakehi*
Faculty of Pharmaceutical Sciences, Kinki University, Kowakae 341, Higashi-Osaka 577-8502, Japan, and Kirin Brewery Co., Ltd., Hagiwara-machi 100-1, Takasaki 370-0013, Japan
J. Proteome Res., 2006, 5 (1), pp 88–97
DOI: 10.1021/pr0502976
Publication Date (Web): December 14, 2005
Copyright © 2006 American Chemical Society

 Kinki University.

,

 Kirin Brewery Co., Ltd.

,
*

 To whom correspondence should be addressed. E-mail:  k_kakehi@ phar.kindai.ac.jp.

Abstract

Abstract Image

Cell surface glycans and recognition molecules of these glycans play important roles in cellular recognition and trafficking, such as in the inflammation response by sialyl LewisX oligosaccharides. Malignant cells also utilize a similar mechanism during colonization and establishment of tumor tissues in the host. These considerations prompt us to develop a screening method for comprehensive analysis of N-glycans derived from membrane fractions of cancer cells. The method involves two step separations. Initially, N-glycans released from cell membrane fractions with N-glycoamidase F were labeled with 2-aminobenzoic acid and separated based on the number of sialic acid residues attached to the oligosaccharides using affinity chromatography on a serotonin-immobilized stationary phase. Each of the nonretarded fractions containing asialo- and high-mannose type oligosaccharides and mono-, di-, tri-, and tetra-sialooligosaccharide fractions which were desialylated with neuraminidase was analyzed by a combination of HPLC using an Amide-80 column as the stationary phase and matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). We analyzed total N-glycan pools of membrane fractions obtained from some cancer cells, and found that U937 cells (Histocytic lymphoma cells) expressed a large amount of oligosaccharides having polylactosamine residues and MKN45 cells (Gastric adenocarcinoma cells) contained hyper-fucosylated oligosaccharides which contained multiple fucose residues. The method described here will be a powerful technique for glycomics studies in cell surface glycoproteins, and will enable one to search marker oligosaccharides characteristically observed in various diseases such as cancer, inflammation, and congenital disorder.

Keywords: cancer cell • N-glycan • serotonin-affinity chromatography • polylactosamine-type oligosaccharide • hyperfucosylated oligosaccharides • MALDI-TOF MS

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History

  • Published In Issue January 06, 2006
  • Received September 4, 2005

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