Glycome mapping on DNA sequencing equipment

被引:150
作者
Laroy, Wouter
Contreras, Roland
Callewaert, Nico
机构
[1] Univ Ghent VIB, Dept Mol Biomed Res, Unit Mol Glycobiol, B-9052 Ghent, Belgium
[2] Univ Ghent VIB, Dept Mol Biomed Res, Unit Fundamental & Appl Mol Biol, B-9052 Ghent, Belgium
关键词
D O I
10.1038/nprot.2006.60
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we provide a detailed protocol for the analysis of protein-linked glycans on DNA sequencing equipment. This protocol satisfies the glyco-analytical needs of many projects and can form the basis of 'glycomics' studies, in which robustness, high throughput, high sensitivity and reliable quantification are of paramount importance. The protocol routinely resolves isobaric glycan stereoisomers, which is much more difficult by mass spectrometry ( MS). Earlier methods made use of polyacrylamide gel-based sequencers, but we have now adapted the technique to multicapillary DNA sequencers, which represent the state of the art today. In addition, we have integrated an option for HPLC-based fractionation of highly anionic 8-amino-1,3,6-pyrenetrisulfonic acid (APTS)-labeled glycans before rapid capillary electrophoretic profiling. This option facilitates either two-dimensional profiling of complex glycan mixtures and exoglycosidase sequencing, or MS analysis of particular compounds of interest rather than of the total pool of glycans in a sample.
引用
收藏
页码:397 / 405
页数:9
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