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72kDa明胶酶A的C末端结构域对于催化作用并非必需,但对于膜激活至关重要,并可调节与金属蛋白酶组织抑制剂的相互作用。

The C-terminal domain of 72 kDa gelatinase A is not required for catalysis, but is essential for membrane activation and modulates interactions with tissue inhibitors of metalloproteinases.

作者信息

Murphy G, Willenbrock F, Ward R V, Cockett M I, Eaton D, Docherty A J

机构信息

Strangeways Research Laboratory, Worts Causeway, Cambridge, U.K.

出版信息

Biochem J. 1992 May 1;283 ( Pt 3)(Pt 3):637-41. doi: 10.1042/bj2830637.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d2c/1130931/0c146cfaf5ba/biochemj00136-0024-a.jpg

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