The thrombospondin motif of aggrecanase-1 (ADAMTS-4) is critical for aggrecan substrate recognition and cleavage

J Biol Chem. 2000 Aug 18;275(33):25791-7. doi: 10.1074/jbc.M001065200.

Abstract

Aggrecanase-1 (ADAMTS-4) is a member of the a disintegrin and metalloprotease with thrombospondin motifs (ADAMTS) protein family that was recently identified. Aggrecanase-1 is one of two ADAMTS cartilage-degrading enzymes purified from interleukin-1-stimulated bovine nasal cartilage (Tortorella, M. D., Burn, T. C., Pratta, M. A. , Abbaszade, I., Hollis, J. M., Liu, R., Rosenfeld, S. A., Copeland, R. A., Decicco, C. P., Wynn, R., Rockwell, A., Yang, F., Duke, J. L., Solomon, K., George, H., Bruckner, R., Nagase, H., Itoh, Y., Ellis, D. M., Ross, H., Wiswall, B. H., Murphy, K., Hillman, M. C., Jr., Hollis, G. F., and Arner, E.C. (1999) Science 284, 1664-1666; 2 Abbaszade, I., Liu, R. Q., Yang, F., Rosenfeld, S. A., Ross, O. H., Link, J. R., Ellis, D. M., Tortorella, M. D., Pratta, M. A., Hollis, J. M., Wynn, R., Duke, J. L., George, H. J., Hillman, M. C., Jr., Murphy, K., Wiswall, B. H., Copeland, R. A., Decicco, C. P., Bruckner, R., Nagase, H., Itoh, Y., Newton, R. C., Magolda, R. L., Trzaskos, J. M., and Burn, T. C. (1999) J. Biol. Chem. 274, 23443-23450). The aggrecan products generated by this enzyme are found in cartilage cultures stimulated with cytokines and in synovial fluid from patients with arthritis, suggesting that aggrecanase-1 may be important in diseases involving cartilage destruction. Here we demonstrate that the thrombospondin type-1 (TSP-1) motif located within the C terminus of aggrecanase-1 binds to the glycosaminoglycans of aggrecan. Data from several studies indicate that this binding of aggrecanase-1 to aggrecan through the TSP-1 motif is necessary for enzymatic cleavage of aggrecan. 1) A truncated form of aggrecanase-1 lacking the TSP-1 motif was not effective in cleaving aggrecan. 2) Several peptides representing different regions of the TSP-1 motif effectively blocked aggrecanase-1 cleavage of aggrecan by preventing the enzyme from binding to the substrate. 3) Aggrecanase-1 was not effective in cleaving glycosaminoglycan-free aggrecan. Taken together, these data suggest that the TSP-1 motif of aggrecanase-1 is critical for substrate recognition and cleavage.

MeSH terms

  • ADAM Proteins
  • ADAMTS4 Protein
  • Aggrecans
  • Amino Acid Motifs
  • Amino Acid Sequence
  • Animals
  • Antibodies, Monoclonal / metabolism
  • Cattle
  • Cell Line
  • Dose-Response Relationship, Drug
  • Drosophila
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme-Linked Immunosorbent Assay
  • Extracellular Matrix Proteins*
  • Glycosylation
  • Inhibitory Concentration 50
  • Kinetics
  • Lectins, C-Type
  • Metalloendopeptidases / chemistry*
  • Molecular Sequence Data
  • Peptides / metabolism
  • Procollagen N-Endopeptidase
  • Protein Binding
  • Proteoglycans / metabolism*
  • Recombinant Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Thrombospondin 1 / chemistry
  • Thrombospondins / chemistry*
  • Time Factors

Substances

  • Aggrecans
  • Antibodies, Monoclonal
  • Extracellular Matrix Proteins
  • Lectins, C-Type
  • Peptides
  • Proteoglycans
  • Recombinant Proteins
  • Thrombospondin 1
  • Thrombospondins
  • thrombospondin 2
  • ADAM Proteins
  • Metalloendopeptidases
  • Procollagen N-Endopeptidase
  • ADAMTS4 Protein