Expression cloning of a cDNA encoding a sulfotransferase involved in the biosynthesis of the HNK-1 carbohydrate epitope

被引:99
作者
Bakker, H
Friedmann, I
Oka, S
Kawasaki, T
Nifantev, N
Schachner, M
Mantei, N
机构
[1] ETH HONGGERBERG,DEPT NEUROBIOL,CH-8093 ZURICH,SWITZERLAND
[2] KYOTO UNIV,FAC PHARMACEUT SCI,DEPT BIOL CHEM,SAKYO KU,KYOTO 60601,JAPAN
[3] RUSSIAN ACAD SCI,ND ZELINSKII ORGAN CHEM INST,MOSCOW 117913,RUSSIA
[4] UNIV HAMBURG,ZENTRUM MOL NEUROBIOL,D-20246 HAMBURG,GERMANY
关键词
D O I
10.1074/jbc.272.47.29942
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 HNK-1 carbohydrate epitope is expressed on several neural adhesion glycoproteins and as a glycolipid, and is involved in cell. interactions, The structural element of the epitope common to glycoproteins and glycolipids has been determined to be sulfate-3-GlcA beta 1-->3Gal beta 1-->4GlcNAc. The glucuronyltransferase and sulfotransferase are considered to be the key enzymes in the biosynthesis of this epitope because the rest of the structure occurs often in glycoconjugates. Here we describe the isolation of the rat sulfotransferase cDNA via an expression cloning strategy, The clone finally isolated predicts a protein of 356 amino acids, uith characteristics of a type II transmembrane protein and with no sequence similarity to other known sulfotransferases, Both the enzyme expressed as a soluble fusion protein and homogenates of cells transfected with the full-length cDNA could transfer sulfate from a sulfate donor to acceptor substrates containing terminal glucuronic acid.
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页码:29942 / 29946
页数:5
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