Glycomics: an integrated systems approach to structure-function relationships of glycans

被引:339
|
作者
Raman, R [1 ]
Raguram, S
Venkataraman, G
Paulson, JC
Sasisekharan, R
机构
[1] MIT, Biol Engn Div, Ctr Biomed Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[2] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
关键词
D O I
10.1038/NMETH807
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In comparison with genomics and proteomics, the advancement of glycomics has faced unique challenges in the pursuit of developing analytical and biochemical tools and biological readouts to investigate glycan structure-function relationships. Glycans are more diverse in terms of chemical structure and information density than are DNA and proteins. This diversity arises from glycans' complex nontemplate-based biosynthesis, which involves several enzymes and isoforms of these enzymes. Consequently, glycans are expressed as an 'ensemble' of structures that mediate function. Moreover, unlike protein-protein interactions, which can be generally viewed as 'digital' in regulating function, glycan-protein interactions impinge on biological functions in a more 'analog' fashion that can in turn 'fine-tune' a biological response. This fine-tuning by glycans is achieved through the graded affinity, avidity and multivalency of their interactions. Given the importance of glycomics, this review focuses on areas of technologies and the importance of developing a bioinformatics platform to integrate the diverse datasets generated using the different technologies to allow a systems approach to glycan structure-function relationships.
引用
收藏
页码:817 / 824
页数:8
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