Murphy G, Willenbrock F, Ward R V, Cockett M I, Eaton D, Docherty A J
Strangeways Research Laboratory, Worts Causeway, Cambridge, U.K.
Biochem J. 1992 May 1;283 ( Pt 3)(Pt 3):637-41. doi: 10.1042/bj2830637.
Recombinant 72 kDa gelatinase A and a truncated form lacking the C-terminal domain were shown to be activated by organomercurials and to possess similar activities towards a number of substrates. The truncated proenzyme differed from the full-length gelatinase in that it could not be activated by a membrane activator and did not bind tissue inhibitor of metalloproteinase (TIMP)-2. Kinetic studies also showed that the inhibition of the activated truncated enzyme, by both TIMP-1 and TIMP-2, was considerably decreased compared with the full-length enzyme. We conclude that the C-terminal domain plays an important role in the regulation of gelatinase A by a potential physiological activator and inhibitors.
重组72 kDa明胶酶A和一种缺少C末端结构域的截短形式被证明可被有机汞激活,并且对多种底物具有相似的活性。截短的酶原与全长明胶酶的不同之处在于,它不能被膜激活剂激活,也不与金属蛋白酶组织抑制剂(TIMP)-2结合。动力学研究还表明,与全长酶相比,TIMP-1和TIMP-2对激活的截短酶的抑制作用明显降低。我们得出结论,C末端结构域在潜在生理激活剂和抑制剂对明胶酶A的调节中起重要作用。