Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/7451
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Variations in the chondroitin sulfate-protein linkage region of aggrecans from bovine nasal and human articular cartilages
Author: Cheng, F.
Heinegard, D.
Fransson, L.A.
Bayliss, M.
Bielicki, J.
Hopwood, J.
Yoshida, K.
Citation: Journal of Biological Chemistry, 1996; 271(45):28572-28580
Publisher: Elsevier BV
Issue Date: 1996
ISSN: 0021-9258
1083-351X
Statement of
Responsibility: 
Fang Cheng, Dick Heinegård, Lars-Åke Fransson, Michael Bayliss, Julie Bielicki, John Hopwood and Keiichi Yoshida
Abstract: Aggrecan-derived chondroitin sulfate (CS) chains, released by beta-elimination, were derivatized with p-aminobenzoic acid or p-aminophenol; radioiodinated; and subjected to graded or complete degradations by chondroitin ABC lyase to generate linkage region fragments of the basic structure DeltaGlyUA-GalNAc-GlcUA-Gal-Gal-Xyl-R (where DeltaGlyUA represents 4, 5-unsaturated glycuronic acid, and R is the adduct), by chondroitin AC lyase to generate the shorter fragment DeltaGlyUA-Gal-Gal-Xyl-R, or by chondroitin C lyase to generate the same fragment when it was linked to a 6-O-sulfated or unsulfated GalNAc at the nonreducing end. Fragments were separated by size using gel chromatography, by charge using ion-exchange chromatography, and by size/charge using electrophoresis and then characterized by stepwise degradations from the nonreducing end by using mercuric acetate to remove all terminal DeltaGlyUA, by bacterial glycuronidase to remove the same residue when linked to unsulfated or 6-O-sulfated GalNAc/Gal, by mammalian 4-sulfatase to remove sulfate from terminal GalNAc 4-O-sulfate, by chondro-4-sulfatase to remove 4-O-sulfate from other GalNAc/Gal residues, and by beta-galactosidase to remove terminal Gal. Results with CS from bovine nasal cartilage aggrecan show that, in nearly all chains, Xyl and probably also the first Gal are unsubstituted, whereas the second Gal is 4-O-sulfated in one CS chain out of five. The first disaccharide repeat is sulfated at C-4 of GalNAc in one chain out of three and unsulfated in the other two. A sulfated first disaccharide is always joined to an unsulfated GlcUA-Gal-Gal sequence. In contrast, CS from human articular cartilage usually has a sulfated first disaccharide repeat. In CS from young human cartilage, sulfate groups are mostly at C-4 of GalNAc in the major part of the chain, but at C-6 in the nonreducing distal portion. In CS from old cartilage, sulfation at C-6 of GalNAc is a major feature from the nonreducing end down to approximately positions 4 and 5 from the linkage region, where GalNAc 4-O-sulfate is common.
Keywords: Nose
Cartilage, Articular
Animals
Cattle
Humans
Chondroitin Sulfates
Proteoglycans
Lectins, C-Type
Extracellular Matrix Proteins
Carbohydrate Sequence
Protein Conformation
Aging
Molecular Sequence Data
Middle Aged
Infant, Newborn
Aggrecans
Chondroitin Sulfate Proteoglycans
DOI: 10.1074/jbc.271.45.28572
Published version: http://dx.doi.org/10.1074/jbc.271.45.28572
Appears in Collections:Aurora harvest 5
Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.