Publication

Crystal structure and carbohydrate-binding properties of the human cartilage glycoprotein-39

Fusetti, F., Pijning, T., Kalk, KH., Bos, E., Dijkstra, BW. & Dijkstra, B. W., 26-Sep-2003, In : The Journal of Biological Chemistry. 278, 39, p. 37753-37760 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

Copy link to clipboard

Documents

DOI

  • F Fusetti
  • T Pijning
  • KH Kalk
  • E Bos
  • BW Dijkstra
  • Bauke W. Dijkstra

The human cartilage glycoprotein-39 (HCgp-39 or YKL40) is expressed by synovial cells and macrophages during inflammation. Its precise physiological role is unknown. However, it has been proposed that HCgp-39 acts as an autoantigen in rheumatoid arthritis, and high expression levels have been associated with cancer development. HCgp-39 shares high sequence homology with family 18 chitinases, and although it binds to chitin it lacks enzymatic activity. The crystal structure of HCgp-39 shows that the protein displays a (beta/alpha)(8)-barrel fold with an insertion of an alpha + beta domain. A 43-Angstrom long carbohydrate-binding cleft is present at the C-terminal side of the beta-strands in the (beta/alpha)(8) barrel. Binding of chitin fragments of different lengths identified nine sugar-binding subsites in the groove. Protein-carbohydrate interactions are mainly mediated by stacking of side chains of aromatic amino acid residues. Surprisingly, the specificity of chitin binding to HCgp-39 depends on the length of the oligosaccharide. Although chitin disaccharides tend to occupy the distal subsites, longer chains bind preferably to the central subsites in the groove. Despite the absence of enzymatic activity, long chitin fragments are distorted upon binding, with the GlcNAc at subsite -1 in a boat conformation, similar to what has been observed in chitinases. The presence of chitin in the human body has never been documented so far. However, the binding features observed in the complex structures suggest that either chitin or a closely related oligosaccharide could act as the physiological ligand for HCgp-39.

Original languageEnglish
Pages (from-to)37753-37760
Number of pages8
JournalThe Journal of Biological Chemistry
Volume278
Issue number39
Publication statusPublished - 26-Sep-2003

    Keywords

  • EARLY RHEUMATOID-ARTHRITIS, CHITINASE PROTEIN FAMILY, SERUM YKL-40, HUMAN CHITOTRIOSIDASE, GLUCOSAMINE RESIDUES, GLYCOSYL HYDROLASES, MAMMALIAN LECTIN, PERIPHERAL-BLOOD, DIFFRACTION DATA, HEPARAN-SULFATE

Download statistics

No data available

ID: 4128583