SEQUENCE-ANALYSIS OF HEPARAN-SULFATE INDICATES DEFINED LOCATION OF N-SULFATED GLUCOSAMINE AND IDURONATE 2-SULFATE RESIDUES PROXIMAL TO THE PROTEIN-LINKAGE REGION

被引:48
作者
TURNBULL, JE [1 ]
GALLAGHER, JT [1 ]
机构
[1] UNIV MANCHESTER,CHRISTIE HOSP & HOLT RADIUM INST,DEPT MED ONCOL,CANC RES CAMPAIGN,MANCHESTER M20 9BX,ENGLAND
关键词
SULFATE PROTEOGLYCANS; GEL ELECTROPHORESIS; DERMATAN SULFATE; MOLECULAR-WEIGHT; MEMBRANE; POLYSACCHARIDES; IDENTIFICATION; BIOSYNTHESIS; FIBROBLASTS; CHAINS;
D O I
10.1042/bj2770297
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
A strategy that we originally used to identify an N-acetylated domain adjacent to the protein-linkage sequence of heparan sulphate proteoglycan (HSPG) [Lyon, Steward, Hampson & Gallagher (1987) Biochem. J. 242, 493-498] has been adapted for analysis of the location of GlcNSO3-HexA and GlcNSO3(+/- 6S)-IdoA(2S) units most proximal to the core protein. [H-3]Glucosamine-labelled HSPG from human skin fibroblasts was depolymerized by using HNO2 or heparinase under conditions that allowed cleavage of all susceptible linkages. The degraded PG was coupled to Sepharose beads through the protein component, enabling specific recovery of protein-linked resistant oligosaccharides. These were released by treatment with alkaline borohydride and analysed by gel filtration and gradient PAGE. This strategy allowed investigation of the sequence of sugar residues along the chain relative to a common reference point (i.e. the reducing end of the chain). HNO2 scission confirmed the presence of a well-defined N-acetylated sequence predominantly 9-12 disaccharide units in length proximal to the core protein. Heparinase scission produced two classes of oligosaccharides (M(r) approx. 7000 and 15 000) with the general formula: IdoA(2S)-GlcNSO3-[HexA-GlcNR]n-HexA-GlcNSO3-[HexA-GlcNAc]9-12-GlcA-Gal-Gal-Xyl in which the average value for n is 1-2 for the 7000-M(r) species and approx. 22 for the 15 000-M(r) species. The latter oligosaccharides extend to about one-third of the total length of the HS chains (M(r) approx. 45 000). HNO2 scission of these oligosaccharides enabled hypothetical models for their sequence to be proposed. The general arrangement of N-sulphated and N-acetylated disaccharides between the proximal GlcNSO3 and terminal IdoA(2S) residues of the 15 000-M(r) fragment was similar to that in the original polysaccharide, suggesting the possibility of a tandemly repeating pattern in the sequence of HS.
引用
收藏
页码:297 / 303
页数:7
相关论文
共 33 条
[1]   REACTION OF HEPARITIN SULFATE WITH NITROUS ACID [J].
CIFONELL.JA .
CARBOHYDRATE RESEARCH, 1968, 8 (02) :233-&
[2]   A METHOD FOR THE SEQUENCE-ANALYSIS OF DERMATAN SULFATE [J].
FRANSSON, LA ;
HAVSMARK, B ;
SILVERBERG, I .
BIOCHEMICAL JOURNAL, 1990, 269 (02) :381-388
[3]  
FRANSSON LA, 1985, J BIOL CHEM, V260, P4722
[4]  
FRANSSON LA, 1989, HEPARIN, P115
[5]   The extended family of proteoglycans: social residents of the pericellular zone [J].
Gallagher, J. T. .
CURRENT OPINION IN CELL BIOLOGY, 1989, 1 (06) :1201-1218
[6]   HEPARAN-SULFATE PROTEOGLYCANS [J].
GALLAGHER, JT ;
TURNBULL, JE ;
LYON, M .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1990, 18 (02) :207-209
[7]   MOLECULAR DISTINCTIONS BETWEEN HEPARAN-SULFATE AND HEPARIN - ANALYSIS OF SULFATION PATTERNS INDICATES THAT HEPARAN-SULFATE AND HEPARIN ARE SEPARATE FAMILIES OF N-SULFATED POLYSACCHARIDES [J].
GALLAGHER, JT ;
WALKER, A .
BIOCHEMICAL JOURNAL, 1985, 230 (03) :665-674
[8]   STRUCTURE AND FUNCTION OF HEPARAN-SULFATE PROTEOGLYCANS [J].
GALLAGHER, JT ;
LYON, M ;
STEWARD, WP .
BIOCHEMICAL JOURNAL, 1986, 236 (02) :313-325
[10]   LOCATION OF ANTITHROMBIN-BINDING REGIONS IN RAT SKIN HEPARIN PROTEOGLYCANS [J].
JACOBSSON, KG ;
LINDAHL, U ;
HORNER, AA .
BIOCHEMICAL JOURNAL, 1986, 240 (03) :625-632