期刊
JOURNAL OF PROTEOME RESEARCH
卷 8, 期 2, 页码 521-537出版社
AMER CHEMICAL SOC
DOI: 10.1021/pr800710f
关键词
O-Glycan; Leukemia cells; Epithelial cancer cells; serotonin-affinity chromatography; MALDI-TOF MS; MSn technique; Glycomics
Recently, we developed an automated apparatus for rapid releasing of O-glycans from mucin-type glycoproteins and proteoglycans (Anal. Biochem. 2007, 362, 245-251; 2007, 371, 52-61). In the present paper, we released O-glycans from some leukemia and epithelial cells using the apparatus, and compared the profiles of O-glycans among these cells after fluorescent labeling of the released glycans with 2-aminobenzoic acid. The fluorescent labeled glycans were analyzed using a combination of HPLC and off-line MALDI-(QIT)TOF mass spectrometry We found that leukemia cells generally showed simple glycan profiles and commonly contained sialyl-T (NeuAc alpha 2-3Gal beta 1-3GalNAc) and disialyl-T (NeuAc alpha 2-3Gal beta 1-3 (NeuAc alpha 2-6)GalNAc) antigens as major O-glycans. In contrast, epithelial cancer cell lines usually showed extremely complex profiles. We found that polylactosamine-type O-glycans were abundantly present in MKN45 cells. Especially, we found characteristic glycans, of which Gal beta 1-3 residue of core1 structure is modified with biantennary polylactosamine units. In contrast, this cell line did not contain polylactosamine-type N-glycans (J. Proteome Res. 2006, 6, 88-97). These results suggest that the different biosynthetic pathways for N- and O-glycans are proposed, The method presented here will accelerate the speed for comprehensive analysis of O-glycans in biological samples and will be a powerful tool for clinical/biochemical analysis in cancer biology.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据