Demonstration of the immature glycosaminoglycan tetrasaccharide sequence GlcAβ1-3Galβ1-3Galβ1-4Xyl on recombinant soluble human α-thrombomodulin -: An oligosaccharide structure on a "part-time" proteoglycan

被引:57
作者
Nadanaka, S [1 ]
Kitagawa, H [1 ]
Sugahara, K [1 ]
机构
[1] Kobe Pharmaceut Univ, Dept Biochem, Higashinada Ku, Kobe, Hyogo 6588558, Japan
关键词
D O I
10.1074/jbc.273.50.33728
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
Thrombomodulin (TM), a cell surface glycoprotein, is a critical mediator of endothelial anticoagulant defenses occurring both as a chondroitin sulfate proteoglycan (beta-TRI) and a protein (alpha-TRI) unsubstituted by chondroitin sulfate (CS), hence its description as a "part-time" proteoglycan (PG) (Fransson , L. A. (1987) Trends Biochem. Sci. 12, 406-411). Sugar analysis was performed on alpha-TM to investigate a possible biosynthetic mechanism for part-time PGs. Recombinant human alpha-TM, which was expressed in CHO-K1 cells, separated by anion-exchange chromatography from beta-TM, and purified by immunoaffinity chromatography (Nawa, K,, Sakano, K., Fujiwara, H., Sate, Y., Sugiyama, N,, Teruuchi, T,, Iwamoto, M., and Marumoto, Y. (1990) Biochem. Biophys. Res. Commun. 171, 729-737), was used for analysis. Preliminary sugar composition analysis after acid hydrolysis showed Xyl in addition to Gal, GalNAc, GlcNAc, Man, Fuc, and Glc. O-Glycosidically-linked oligosaccharides were liberated by mild alkaline treatment and purified. The isolated oligosaccharide fraction was derivatized with a fluorophore 2-aminobenzamide (2AB), resulting in two fluorescent components, a 2AB-oligosaccharide and a putative 2AB-Glc. Based on structural analysis by a combination of sequential exoglycosidase digestion and 500-MHz H-1 NMR spectroscopy of the 2AB-oligosaccharide, the structure of the oligosaccharide was elucidated as GlcA beta 1-3Gal beta 1-3Gal beta 1-4Xyl, which turned out to represent a glycosaminoglycan (GAG)-protein linkage region tetrasaccharide common to various PGs and was considered to be a biosynthetic intermediate of an immature GAG chain. The results may indicate that at least one class of the so-called part-time PGs bear the linkage tetrasaccharide at the GAG attachment sites and that the critical determining step or the rate-limiting step for PG: biosynthesis is the transfer of the fifth sugar residue, the first hexosamine, rather than xylose.
引用
收藏
页码:33728 / 33734
页数:7
相关论文
共 46 条
[41]   BETA-GLUCURONIDASE FROM AMPULLARIA PURIFICATION AND KINETIC-PROPERTIES [J].
TSUKADA, T ;
YOSHINO, M .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1987, 86 (03) :565-569
[42]  
VERTEL BM, 1993, J BIOL CHEM, V268, P11105
[43]   HIGH-RESOLUTION, H-1-NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY AS A TOOL IN THE STRUCTURAL-ANALYSIS OF CARBOHYDRATES RELATED TO GLYCOPROTEINS [J].
VLIEGENTHART, JFG ;
DORLAND, L ;
VANHALBEEK, H .
ADVANCES IN CARBOHYDRATE CHEMISTRY AND BIOCHEMISTRY, 1983, 41 :209-374
[44]   THE SULFATED CARBOHYDRATE-PROTEIN LINKAGE REGION ISOLATED FROM CHONDROITIN 4-SULFATE CHAINS OF INTER-ALPHA-TRYPSIN INHIBITOR IN HUMAN PLASMA [J].
YAMADA, S ;
OYAMA, M ;
KINUGASA, H ;
NAKAGAWA, T ;
KAWASAKI, T ;
NAGASAWA, S ;
KHOO, KH ;
MORRIS, HR ;
DELL, A ;
SUGAHARA, K .
GLYCOBIOLOGY, 1995, 5 (03) :335-341
[45]  
YE J, 1993, J BIOL CHEM, V268, P2373
[46]  
ZHANG LJ, 1994, J BIOL CHEM, V269, P19295