The repertoire of glycan determinants in the human glycome

被引:375
作者
Cummings, Richard D. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Biochem, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
BLOOD-GROUP-A; SELECTIN GLYCOPROTEIN LIGAND-1; N-LINKED OLIGOSACCHARIDE; ENDO-BETA-GALACTOSIDASE; SIALYL-LEWIS-X; ANTITHROMBIN-BINDING SEQUENCE; RICINUS-COMMUNIS AGGLUTININ; HIGH ENDOTHELIAL VENULES; PROTEIN LINKAGE REGION; RAY CRYSTAL-STRUCTURE;
D O I
10.1039/b907931a
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
The number of glycan determinants that comprise the human glycome is not known. This uncertainty arises from limited knowledge of the total number of distinct glycans and glycan structures in the human glycome, as well as limited information about the glycan determinants recognized by glycan-binding proteins (GBPs), which include lectins, receptors, toxins, microbial adhesins, antibodies, and enzymes. Available evidence indicates that GBP binding sites may accommodate glycan determinants made up of 2 to 6 linear monosaccharides, together with their potential side chains containing other sugars and modi. cations, such as sulfation, phosphorylation, and acetylation. Glycosaminoglycans, including heparin and heparan sulfate, comprise repeating disaccharide motifs, where a linear sequence of 5 to 6 monosaccharides may be required for recognition. Based on our current knowledge of the composition of the glycome and the size of GBP binding sites, glycoproteins and glycolipids may contain similar to 3000 glycan determinants with an additional similar to 4000 theoretical pentasaccharide sequences in glycosaminoglycans. These numbers provide an achievable target for new chemical and/or enzymatic syntheses, and raise new challenges for de. ning the total glycome and the determinants recognized by GBPs.
引用
收藏
页码:1087 / 1104
页数:18
相关论文
共 345 条
[1]   Partial characterization of the N-linked oligosaccharide structures on P-selectin glycoprotein ligand-1 (PSGL-1) [J].
Aeed, PA ;
Geng, JG ;
Asa, D ;
Raycroft, L ;
Ma, L ;
Elhammer, ÅP .
CELL RESEARCH, 2001, 11 (01) :28-36
[2]   THE STRUCTURAL RELATION BETWEEN THE ANTIGENIC DETERMINANTS TO MONOCLONAL-ANTIBODIES AND BINDING-SITES TO RAT-BRAIN SYNAPTOSOMES AND GT1B GANGLIOSIDE IN CLOSTRIDIUM-BOTULINUM TYPE-C NEUROTOXIN [J].
AGUI, T ;
SYUTO, B ;
OGUMA, K ;
IIDA, H ;
KUBO, S .
JOURNAL OF BIOCHEMISTRY, 1985, 97 (01) :213-218
[3]   A GANGLIOSIDE ANTIGEN ON THE RAT PANCREATIC B-CELL SURFACE IDENTIFIED BY MONOCLONAL-ANTIBODY R2D6 [J].
ALEJANDRO, R ;
SHIENVOLD, FL ;
HAJEK, SAV ;
PIERCE, M ;
PAUL, R ;
MINTZ, DH .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 74 (01) :25-38
[4]  
ALVAREZ JG, 1990, J LIPID RES, V31, P1073
[5]   Identification of ligand specificities for glycan-binding proteins using glycan arrays [J].
Alvarez, Richard A. ;
Blixt, Ola .
GLYCOBIOLOGY, 2006, 415 :292-310
[6]   A clostridial endo-β-galactosidase that cleaves both blood group A and B glycotopes [J].
Anderson, KM ;
Ashida, H ;
Maskos, K ;
Dell, A ;
Li, SC ;
Li, YT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (09) :7720-7728
[7]  
ANDO S, 1982, ADV EXP MED BIOL, V152, P71
[8]   Chemical diversity in the sialic acids and related α-keto acids:: An evolutionary perspective [J].
Angata, T ;
Varki, A .
CHEMICAL REVIEWS, 2002, 102 (02) :439-469
[9]  
Aoki Kiyoko F, 2003, Genome Inform, V14, P134
[10]   On the frequency of protein glycosylation, as deduced from analysis of the SWISS-PROT database [J].
Apweiler, R ;
Hermjakob, H ;
Sharon, N .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1999, 1473 (01) :4-8