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The sulphated carbohydrate-protein linkage region isolated from chondroitin 4-sulphate chains of inter-α-trypsin inhibitor in human plasma

Inter-α-trypsin inhibitor (ITI) in human plasma has a unique structural architecture composed of three polypeptide chains (H1, H2 and L chains), which are linked to each other through a chondroitin 4-sulphate chain. The structure of the carbohydrate-protein linkage region of the chondroitin 4-sulpha...

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Published in:Glycobiology (Oxford) 1995-05, Vol.5 (3), p.335-341
Main Authors: Yamada, Shuhei, Oyama, Mika, Kinugasa, Hitoko, Nakagawa, Tomoyo, Kawasaki, Toshisuke, Nagasawa, Shigeharu, Khoo, Kay-Hooi, Morris, Howard R., Dell, Anne, Sugahara, Kazuyuki
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container_issue 3
container_start_page 335
container_title Glycobiology (Oxford)
container_volume 5
creator Yamada, Shuhei
Oyama, Mika
Kinugasa, Hitoko
Nakagawa, Tomoyo
Kawasaki, Toshisuke
Nagasawa, Shigeharu
Khoo, Kay-Hooi
Morris, Howard R.
Dell, Anne
Sugahara, Kazuyuki
description Inter-α-trypsin inhibitor (ITI) in human plasma has a unique structural architecture composed of three polypeptide chains (H1, H2 and L chains), which are linked to each other through a chondroitin 4-sulphate chain. The structure of the carbohydrate-protein linkage region of the chondroitin 4-sulphate chain attached to the L chain was investigated. The peptide-chondroitin sulphate fraction was isolated by anion-exchange chromatography after exhaustive digestion with lysyl endopeptidase and then V8 protease. The chondroitin 4-sulphate chain was released from the peptides by β-elimination using NaB3H4, and then digested with chondroitinase ABC. These treatments resulted In a single 3H-labelled hexasaccharide alditol fraction derived from the linkage region which had been associated with the L chain. Chemical and enzymatic analyses as well as fast-atom bombardment-mass spectrometry (FAB-MS) analysis revealed that the 3H-labelled hexasaccharide alditol had the following structure:δHexAα1-3GalNAc(4-sulphate)β1-4GlcAβ1-3Gal(4-sulphate)β1-3Galβ1-4Xyl-ol (where ΔHexA is 4-deoxy-α-L-threo-hex-4-enepyranosyluronic acid and Xyl-ol is xylitol). The structure contained the novel 4-sulphated Gal residue, which was previously demonstrated in a linkage hexasaccharide isolated from chondroitin 4-sulphate of rat chondrosarcoma (Sugahara et al., J. Biol Chem., 263,10168–10174, 1988) and of whale cartilage (Sugahara et al., Eur. J. Biochem., 202, 805–811, 1991). The above disulphated hexasaccharide alditol was the only component detected in the linkage region fraction of the chondroitin 4-sulphate chain of ITI, which implies some biological significance of this novel structure.
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Oyama, Mika ; Kinugasa, Hitoko ; Nakagawa, Tomoyo ; Kawasaki, Toshisuke ; Nagasawa, Shigeharu ; Khoo, Kay-Hooi ; Morris, Howard R. ; Dell, Anne ; Sugahara, Kazuyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c243t-f483bb6e4fac94012440c35ad89157f3e275d6575dd06e34116c1d09828c7cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Alpha-Globulins - chemistry</topic><topic>Amino Acid Sequence</topic><topic>Carbohydrate Sequence</topic><topic>Carbohydrates - chemistry</topic><topic>Carbohydrates - isolation &amp; purification</topic><topic>Chondroitin Sulfates - chemistry</topic><topic>chondroitin sulphate</topic><topic>FAB-MS</topic><topic>Glycopeptides - chemistry</topic><topic>Humans</topic><topic>inter-α-trypsin inhibitor</topic><topic>Molecular Sequence Data</topic><topic>Proteins - chemistry</topic><topic>Proteins - isolation &amp; purification</topic><topic>Spectrometry, Mass, Fast Atom Bombardment</topic><topic>sulphated oligosaccharides</topic><topic>Trypsin Inhibitors - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamada, Shuhei</creatorcontrib><creatorcontrib>Oyama, Mika</creatorcontrib><creatorcontrib>Kinugasa, Hitoko</creatorcontrib><creatorcontrib>Nakagawa, Tomoyo</creatorcontrib><creatorcontrib>Kawasaki, Toshisuke</creatorcontrib><creatorcontrib>Nagasawa, Shigeharu</creatorcontrib><creatorcontrib>Khoo, Kay-Hooi</creatorcontrib><creatorcontrib>Morris, Howard R.</creatorcontrib><creatorcontrib>Dell, Anne</creatorcontrib><creatorcontrib>Sugahara, Kazuyuki</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Glycobiology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamada, Shuhei</au><au>Oyama, Mika</au><au>Kinugasa, Hitoko</au><au>Nakagawa, Tomoyo</au><au>Kawasaki, Toshisuke</au><au>Nagasawa, Shigeharu</au><au>Khoo, Kay-Hooi</au><au>Morris, Howard R.</au><au>Dell, Anne</au><au>Sugahara, Kazuyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The sulphated carbohydrate-protein linkage region isolated from chondroitin 4-sulphate chains of inter-α-trypsin inhibitor in human plasma</atitle><jtitle>Glycobiology (Oxford)</jtitle><addtitle>Glycobiology</addtitle><date>1995-05</date><risdate>1995</risdate><volume>5</volume><issue>3</issue><spage>335</spage><epage>341</epage><pages>335-341</pages><issn>0959-6658</issn><eissn>1460-2423</eissn><abstract>Inter-α-trypsin inhibitor (ITI) in human plasma has a unique structural architecture composed of three polypeptide chains (H1, H2 and L chains), which are linked to each other through a chondroitin 4-sulphate chain. The structure of the carbohydrate-protein linkage region of the chondroitin 4-sulphate chain attached to the L chain was investigated. The peptide-chondroitin sulphate fraction was isolated by anion-exchange chromatography after exhaustive digestion with lysyl endopeptidase and then V8 protease. The chondroitin 4-sulphate chain was released from the peptides by β-elimination using NaB3H4, and then digested with chondroitinase ABC. These treatments resulted In a single 3H-labelled hexasaccharide alditol fraction derived from the linkage region which had been associated with the L chain. Chemical and enzymatic analyses as well as fast-atom bombardment-mass spectrometry (FAB-MS) analysis revealed that the 3H-labelled hexasaccharide alditol had the following structure:δHexAα1-3GalNAc(4-sulphate)β1-4GlcAβ1-3Gal(4-sulphate)β1-3Galβ1-4Xyl-ol (where ΔHexA is 4-deoxy-α-L-threo-hex-4-enepyranosyluronic acid and Xyl-ol is xylitol). The structure contained the novel 4-sulphated Gal residue, which was previously demonstrated in a linkage hexasaccharide isolated from chondroitin 4-sulphate of rat chondrosarcoma (Sugahara et al., J. Biol Chem., 263,10168–10174, 1988) and of whale cartilage (Sugahara et al., Eur. J. Biochem., 202, 805–811, 1991). The above disulphated hexasaccharide alditol was the only component detected in the linkage region fraction of the chondroitin 4-sulphate chain of ITI, which implies some biological significance of this novel structure.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>7544656</pmid><doi>10.1093/glycob/5.3.335</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0959-6658
ispartof Glycobiology (Oxford), 1995-05, Vol.5 (3), p.335-341
issn 0959-6658
1460-2423
language eng
recordid cdi_proquest_miscellaneous_77481973
source Oxford University Press Archive
subjects Alpha-Globulins - chemistry
Amino Acid Sequence
Carbohydrate Sequence
Carbohydrates - chemistry
Carbohydrates - isolation & purification
Chondroitin Sulfates - chemistry
chondroitin sulphate
FAB-MS
Glycopeptides - chemistry
Humans
inter-α-trypsin inhibitor
Molecular Sequence Data
Proteins - chemistry
Proteins - isolation & purification
Spectrometry, Mass, Fast Atom Bombardment
sulphated oligosaccharides
Trypsin Inhibitors - chemistry
title The sulphated carbohydrate-protein linkage region isolated from chondroitin 4-sulphate chains of inter-α-trypsin inhibitor in human plasma
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