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In trans interaction of hepatitis C virus helicase domains mediates protease activity critical for internal NS3 cleavage and cell transformation.
- Source :
-
FEBS letters [FEBS Lett] 2010 Feb 05; Vol. 584 (3), pp. 482-6. Date of Electronic Publication: 2009 Dec 03. - Publication Year :
- 2010
-
Abstract
- Hepatitis C virus (HCV) internal non-structural protein 3 (NS3) cleavage can occur in trans in the presence of NS4A. In this study, we have further demonstrated a critical role of the helicase domain in the internal NS3 cleavage, different from HCV polyprotein processing which requires only the serine protease domain. The NTPase domain of NS3 helicase interacts with the RNA binding domain to facilitate internal NS3 cleavage. In addition, NS3 protease activity contributes to the transforming ability of the major internal cleavage product NS3(1-402). These findings imply important roles of the internal cleavage and protease activity of the NS3 protein in the pathogenesis of HCV.<br /> (2009 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Binding Sites
Cell Line
Cell Line, Tumor
Hepacivirus genetics
Humans
Mice
NIH 3T3 Cells
Polyproteins genetics
Polyproteins metabolism
Protein Binding
Protein Structure, Secondary
Protein Structure, Tertiary genetics
Protein Structure, Tertiary physiology
RNA Helicases chemistry
RNA Helicases genetics
Serine Proteases chemistry
Serine Proteases genetics
Serine Proteases metabolism
Viral Nonstructural Proteins chemistry
Viral Nonstructural Proteins genetics
Hepacivirus enzymology
RNA Helicases metabolism
Viral Nonstructural Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3468
- Volume :
- 584
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- FEBS letters
- Publication Type :
- Academic Journal
- Accession number :
- 19958771
- Full Text :
- https://doi.org/10.1016/j.febslet.2009.11.090