Cloning of rat 92-kDa type IV collagenase and expression of an active recombinant catalytic domain

被引：20

作者：

Xia, YY ^{[1
]}

Garcia, G ^{[1
]}

Chen, SZ ^{[1
]}

Wilson, CB ^{[1
]}

Feng, LL ^{[1
]}

机构：

[1] Scripps Res Inst, DEPT IMMUNOL, LA JOLLA, CA 92037 USA

来源：

FEBS LETTERS | 1996年 / 382卷 / 03期

关键词：

metalloproteinase; MMP-9; eukaryotic expression; prokaryotic expression; refolding;

D O I：

10.1016/0014-5793(96)00185-8

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

A full-length cDNA for rat 92-kDa type IV collagenase was isolated and sequenced. RNase protection assay revealed tissue specific differential expression of the 92-kDa type IV collagenase in the rat during development. Natural and modified forms of the 92-kDa type IV collagenase were expressed. One active protein, 92-CD, contained only the putative catalytic domain. Large quantities of the 92-CD were expressed in Escherichia coli, extracted from inclusion bodies, purified, and refolded to an active form. This recombinant protein was able to cleave denatured and native collagen and was inactivated by known MMP inhibitors.

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收藏

页码：285 / 288

页数：4

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