Mutations in the interglobular domain of aggrecan alter matrix metalloproteinase and aggrecanase cleavage patterns. Evidence that matrix metalloproteinase cleavage interferes with aggrecanase activity

• Published in: The Journal of biological chemistry Vol. 275; no. 42; pp. 33038 - 33045
• Main Authors: Mercuri, F A, Maciewicz, R A, Tart, J, Last, K, Fosang, A J
• Format: Journal Article
• Language: English
• Published: United States 20.10.2000
• Subjects: aggrecan; Aggrecans; Amino Acid Sequence; Animals; Base Sequence; Binding Sites; Chondroitin Sulfate Proteoglycans - chemistry; Chondroitin Sulfate Proteoglycans - metabolism; Collagenases - metabolism; DNA Primers; Endopeptidases - metabolism; Enzyme Precursors - metabolism; Extracellular Matrix Proteins; Gelatinases - metabolism; Humans; Lectins, C-Type; Matrix metalloproteinase; Matrix Metalloproteinase 1; Matrix Metalloproteinase 9 - metabolism; Matrix Metalloproteinases - metabolism; Metalloendopeptidases - metabolism; mmp13 gene; Molecular Sequence Data; Mutagenesis, Site-Directed; Proteoglycans - chemistry; Proteoglycans - genetics; Proteoglycans - metabolism; Recombinant Proteins - chemistry; Recombinant Proteins - metabolism; Spodoptera; Substrate Specificity; Tissue Inhibitor of Metalloproteinase-1 - metabolism
• ISSN: 0021-9258
• DOI: 10.1074/jbc.275.42.33038

We have expressed G1-G2 mutants with amino acid changes at the DIPEN(341) downward arrow(342)FFGVG and ITEGE(373) downward arrow(374)ARGSV cleavage sites, in order to investigate the relationship between matrix metalloproteinase (MMP) and aggrecanase activities in the interglobular domain (IGD) of aggrecan. The mutation DIPEN(341) to DIGSA(341) partially blocked cleavage by MMP-13 and MMP-8 at the MMP site, while the mutation (342)FFGVG to (342)GTRVG completely blocked cleavage at this site by MMP-1, -2, -3, -7, -8, -9, -13, -14. Each of the MMP cleavage site mutants, including a four-amino acid deletion mutant lacking residues ENFF(343), were efficiently cleaved by aggrecanase, suggesting that the primary sequence at the MMP site had no effect on aggrecanase activity in the IGD. The mutation (374)ARGSV to (374)NVYSV completely blocked cleavage at the aggrecanase site by aggrecanase, MMP-8 and atrolysin C but had no effect on the ability of MMP-8 and MMP-13 to cleave at the Asn(341) downward arrowPhe bond. Susceptibility to atrolysin C cleavage at the MMP site was conferred in the DIGSA(341) mutant but absent in the wild-type, (342)GTRVG, (374)NVYSV, and deletion mutants. To further explore the relationship between MMP and aggrecanase activities, sequential digest experiments were done in which MMP degradation products were subsequently digested with aggrecanase and vice versa. Aggrecanase-derived G1 domains with ITEGE(373) C termini were viable substrates for MMPs; however, MMP-derived G2 fragments were resistant to cleavage by aggrecanase. A 10-mer peptide FVDIPENFFG, which is a substrate analogue for the MMP cleavage site, inhibited aggrecanase cleavage at the Glu(373) downward arrowAla bond. This study demonstrates that MMPs and aggrecanase have unique substrate recognition in the IGD of aggrecan and suggests that sequences at the C terminus of the DIPEN(341) G1 domain may be important for regulating aggrecanase cleavage.