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.
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页码:33728 / 33734
页数:7
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共 46 条
[1]  
ASPINALL GO, 1982, POLSACCHARIDES, V1, P37
[2]  
BIGGE JC, 1995, ANAL BIOCHEM, V230, P616
[3]   IDENTIFICATION AND SYNTHESIS OF A RECOGNITION SIGNAL FOR THE ATTACHMENT OF GLYCOSAMINOGLYCANS TO PROTEINS [J].
BOURDON, MA ;
KRUSIUS, T ;
CAMPBELL, S ;
SCHWARTZ, NB ;
RUOSLAHTI, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (10) :3194-3198
[4]   FUNCTIONAL DOMAINS OF RABBIT THROMBOMODULIN [J].
BOURIN, MC ;
BOFFA, MC ;
BJORK, I ;
LINDAHL, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :5924-5928
[5]  
CHEIFETZ S, 1988, J BIOL CHEM, V263, P16984
[6]  
DEWAARD P, 1992, J BIOL CHEM, V267, P6036
[7]  
DITTMAN WA, 1990, BLOOD, V75, P329
[8]   Platelet factor 4 binds to glycanated forms of thrombomodulin and to protein C - A potential mechanism for enhancing generation of activated protein C [J].
Dudek, AZ ;
Pennell, CA ;
Decker, TD ;
Young, TA ;
Key, NS ;
Slungaard, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (50) :31785-31792
[9]  
ESMON CT, 1989, J BIOL CHEM, V264, P4743
[10]   STRUCTURE AND FUNCTION OF CELL-ASSOCIATED PROTEOGLYCANS [J].
FRANSSON, LA .
TRENDS IN BIOCHEMICAL SCIENCES, 1987, 12 (10) :406-411