THE GELATIN-BINDING SITE OI HUMAN 72 KDA TYPE-IV COLLAGENASE (GELATINASE A)

被引:71
作者
BANYAI, L [1 ]
TORDAI, H [1 ]
PATTHY, L [1 ]
机构
[1] HUNGARIAN ACAD SCI,BIOL RES CTR,INST ENZYMOL,H-1518 BUDAPEST,HUNGARY
关键词
D O I
10.1042/bj2980403
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
To identify structures critical for gelatin-binding of 72 kDa type IV collagenase (gelatinase A), fragments of this metalloproteinase have been expressed in Escherichia coli and assayed for their gelatin affinity. Each of the three fibronectin-related type II domains was found to have affinity for gelatin. Fragments containing all three tandem type II domains had significantly stronger affinity than any of the constituent units, indicating that they co-operate to form the high-affinity gelatin-binding site. Competition experiments have also shown that gelatinase A binds more tightly to gelatin than fibronectin and can displace the latter from denatured collagen.
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页码:403 / 407
页数:5
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