BlotGIycoABC™, an integrated glycoblotting technique for rapid and large scale clinical glycomics

被引:66
作者
Miura, Yoshiaki [1 ,2 ]
Hato, Megumi [1 ,2 ]
Shinohara, Yasuro [1 ,2 ]
Kuramoto, Hiromitsu [3 ]
Furukawa, Jun-ichi [1 ,2 ]
Kurogochi, Masaki [1 ,2 ]
Shimaoka, Hideyuki [3 ]
Tada, Mitsuhiro [4 ]
Nakanishi, Kazuaki [5 ]
Ozaki, Michitaka [5 ]
Todo, Satoru [5 ]
Nishimura, Shin-Ichiro [1 ,2 ]
机构
[1] Hokkaido Univ, Ctr Post Gen Sci & Technol, Grad Sch Life Sci, Sapporo, Hokkaido 0010021, Japan
[2] Hokkaido Univ, Ctr Post Gen Sci & Technol, Frontier Res Ctr, Sapporo, Hokkaido 0010021, Japan
[3] Sumitomo Bakelite Co, Kobe, Hyogo 6512241, Japan
[4] Hokkaido Univ, Inst Med Genet, Div Canc Related Genes, Sapporo, Hokkaido 0600815, Japan
[5] Hokkaido Univ, Grad Sch Med, Dept Gen Surg, Sapporo, Hokkaido 0608638, Japan
关键词
D O I
10.1074/mcp.M700377-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recent progress in mass spectrometry has led to new challenges in glycomics, including the development of rapid glycan enrichment techniques. A facile technique for exploration of a carbohydrate-related biomarker is important because proteomics research targets glycosylation, a posttranslational modification. Here we report an "all-in-one" protocol for high throughput clinical glycomics. This new technique integrates glycoblotting-based glycan enrichment onto the BlotGlycoABC(TM) bead, on-bead stabilization of sialic acids, and fluorescent labeling of oligosaccharides in a single workflow on a multiwell filter plate. The advantage of this protocol and MALDI-TOF MS was demonstrated through differentiation of serum N-glycan profiles of subjects with congenital disorders of glycosylation and hepatocellular carcinoma and healthy donors. The method also permitted total cellular glycomics analysis of human prostate cancer cells and normal human prostate epithelial cells. These results demonstrate the potentials of glycan enrichment/processing for biomarker discovery.
引用
收藏
页码:370 / 377
页数:8
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