Glycomics approach to structure-function relationships of glycosaminoglycans

被引:218
作者
Sasisekharan, Ram [1 ]
Raman, Rahul [1 ]
Prabhakar, Vikas [1 ]
机构
[1] MIT, Ctr Biomed Engn, Biol Engn Div, Cambridge, MA 02139 USA
关键词
cancer; anticoagulation; heparin; heparan; chondroitin; dermatan;
D O I
10.1146/annurev.bioeng.8.061505.095745
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Extracellular modulation of phenotype is an emerging paradigm in this current postgenomics age of molecular and cell biology. Glycosaminoglycans (GAGs) are primary components of the cell surface and the cell-extracellular matrix (ECM) interface. Advances in the technology to analyze GAGs and in whole-organism genetics have led to a dramatic increase in the known important biological role of these complex polysaccharides. Owing to their ubiquitous distribution at the cell-ECM interface, GAGs interact with numerous proteins and modulate their activity, thus impinging on fundamental biological processes such as cell growth and development. Many recent reviews have captured important aspects of GAG structure and biosynthesis, GAG-protein interactions, and GAG biology. GAG research is currently at a stage where there is a need for an integrated systems or glycomics approach, which involves an integration of all of the above concepts to define their structure-function relationships. Focusing on heparin/heparan (I-ISGAGs) and chondroitin/dermatan sulfate (CSGAGs), this review highlights the important aspects of GAGs and summarizes these aspects in the context of taking a glycomics approach that integrates the different technologies to define structure-function relationships of GAGs.
引用
收藏
页码:181 / 231
页数:51
相关论文
共 209 条
[1]   Substrate specificity and domain functions of extracellular heparan sulfate 6-O-endosulfatases, QSulf1 and QSulf2 [J].
Ai, XB ;
Do, AT ;
Kusche-Gullberg, M ;
Lindahl, U ;
Lu, K ;
Emerson, CP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (08) :4969-4976
[2]   DERMATAN SULFATE AND CHONDROITIN 6-SULFATE CONFORMATIONS [J].
ARNOTT, S ;
GUSS, JM ;
HUKINS, DWL ;
MATHEWS, MB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1973, 54 (04) :1377-1383
[3]  
ATKINS EDT, 1976, HEPARIN CHEM CLIN US, P21
[4]   A coarse-grained molecular model for glycosaminoglycans: Application to chondroitin, chondroitin sulfate, and hyaluronic acid [J].
Bathe, M ;
Rutledge, GC ;
Grodzinsky, AJ ;
Tidor, B .
BIOPHYSICAL JOURNAL, 2005, 88 (06) :3870-3887
[5]   Syndecans in tumor cell adhesion and signaling [J].
Beauvais D.M. ;
Rapraeger A.C. .
Reproductive Biology and Endocrinology, 2 (1)
[6]   Quantification of isomers from a mixture of twelve heparin and heparan sulfate disaccharides using tandem mass spectrometry [J].
Behr, JR ;
Matsumoto, Y ;
White, FM ;
Sasisekharan, R .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2005, 19 (18) :2553-2562
[7]  
Benowitz LI, 2002, PROG BRAIN RES, V137, P389
[8]  
Berry D, 2004, CHEM BIOL, V11, P487, DOI 10.1016/j.chembiol.2004.03.023
[9]  
Binari RC, 1997, DEVELOPMENT, V124, P2623
[10]   Binding of endostatin to endothelial heparan sulphate shows a differential requirement for specific sulphates [J].
Blackhall, FH ;
Merry, CLR ;
Lyon, M ;
Jayson, GC ;
Folkman, J ;
Javaherian, K ;
Gallagher, JT .
BIOCHEMICAL JOURNAL, 2003, 375 :131-139