Fosang A J, Last K, Neame P J, Murphy G, Knäuper V, Tschesche H, Hughes C E, Caterson B, Hardingham T E
University of Melbourne, Department of Medicine, Royal Melbourne Hospital, Parkville, Australia.
Biochem J. 1994 Dec 1;304 ( Pt 2)(Pt 2):347-51. doi: 10.1042/bj3040347.
Native and recombinant neutrophil collagenase (MMP-8) was shown to cleave at the E373-A374 'aggrecanase' site in the interglobular domain of aggrecan. The time course of digestion in vitro showed that MMP-8 cleaved initially at N341-F342, the predominant metalloproteinase site, before cleaving at the E373-A374 site. A synthetic peptide, IPENFFG, inhibited cleavage at E373-A374 but not N341-F342 in vitro, indicating that the E373-A374 sequence was a less preferred site for MMP-8 cleavage than N341-F342. IPENFFG also inhibited release of A374 RGSVI fragments from cartilage in explant culture, suggesting that a metalloproteinase cleaved at the aggrecanase site in situ. The possibility remains that 'aggrecanase' may be a metalloproteinase in cartilage.
天然和重组中性粒细胞胶原酶(基质金属蛋白酶-8,MMP-8)可在聚集蛋白聚糖球间结构域的E373-A374“聚集蛋白聚糖酶”位点进行切割。体外消化的时间进程表明,MMP-8最初在主要的金属蛋白酶位点N341-F342处切割,然后才在E373-A374位点切割。一种合成肽IPENFFG在体外可抑制E373-A374处的切割,但不能抑制N341-F342处的切割,这表明E373-A374序列相比N341-F342序列,是MMP-8切割的较不优先选择的位点。IPENFFG还可抑制外植体培养中软骨释放A374 RGSVI片段,这表明一种金属蛋白酶在原位的聚集蛋白聚糖酶位点进行切割。“聚集蛋白聚糖酶”仍有可能是软骨中的一种金属蛋白酶。