Analyzing the dynamic bacterial glycome with a lectin microarray approach

被引:197
作者
Hsu, KL [1 ]
Pilobello, KT [1 ]
Mahal, LK [1 ]
机构
[1] Univ Texas, Inst Cellular & Mol Biol, Ctr Syst & Synth Biol, Dept Chem & Biochem, Austin, TX 78712 USA
关键词
D O I
10.1038/nchembio767
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glycosylation of bacterial cell surfaces is emerging as a critical factor in symbiosis, pathogenesis, cell-cell interactions and immune evasion(1-3). The lack of high-throughput analytical tools to examine bacterial glycans has been a major obstacle to the field and has hindered closer examination of the dynamics of carbohydrate variation. We have recently developed a lectin microarray for the analysis of glycoproteins(4). Herein we present a rapid analytical system based on this technology for the examination of bacterial glycans. The glycosylation pattern observed distinguishes closely related Escherichia coli strains from one another, providing a facile means of fingerprinting bacteria. In addition, dynamic alterations in the carbohydrate coat of a pathogenic E. coli strain are readily observed. The fast evaluation of real-time alterations in surface-carbohydrate epitopes allows examination of the dynamic role of bacterial sugars in response to external stimuli such as the immune system.
引用
收藏
页码:153 / 157
页数:5
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