GB virus B and hepatitis C virus NS3 serine proteases share substrate specificity

被引:39
作者
Scarselli, E [1 ]
Urbani, A [1 ]
Sbardellati, A [1 ]
Tomei, L [1 ]
DeFrancesco, R [1 ]
Traboni, C [1 ]
机构
[1] IST RIC BIOL MOL P ANGELETTI,I-00040 POMEZIA,ROMA,ITALY
关键词
D O I
10.1128/JVI.71.7.4985-4989.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
GB virus B (GBV-B) is a recently discovered virus responsible for hepatitis in tamarins (Saguinus species), GBV-B belongs to the Flaviviridae family and is closely related to the human pathogen hepatitis C virus (HCV). Nonstructural protein 3 (NS3) of HCV has been shown to encompass a serine protease domain required for viral maturation. GBV-B and HCV share only about 30% of the amino acid sequence within the NS3 protease domain, The catalytic triad is conserved, and the residue Phe-154, presumed to be a crucial amino acid for determining the S-1 specificity pocket of the HCV NS3 protease, is also conserved, We have expressed a synthetic gene encoding the GBV-B NS3 protease domain in Escherichia coli and have characterized the purified recombinant protein for its activity on HCV substrates, We have shown that the NS3 region of the GBV-B genome actually encodes a serine protease that, despite the low sequence homology, shares substrate specificity with the HCV NS3 protease.
引用
收藏
页码:4985 / 4989
页数:5
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