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Structure and Functions of Hepatitis C Virus Proteins: 15 Years After

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Publisher Springer
Specialty Microbiology
Date 2007 Apr 26
PMID 17455808
Citations 8
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Abstract

Since its discovery in 1988, the hepatitis C virus (HCV) has become a hot topic of research by many groups around the world. This globally spread infectious agent is responsible for a large proportion of chronic viral hepatitides. The clue to halting the hepatitis C pandemic may be the detailed understanding of the virus structure, its replication mechanism, and the exact functions of the various proteins. Such understanding could enable the development of new antivirals targeted against hepatitis C virus and possibly an effective vaccine. This review recaps the current knowledge about the HCV genome 15 years after its discovery. The structure and function of particular viral structural (core, E1, E2) and nonstructural (NS2, NS3, NS4, NS5) proteins and noncoding regions known to date are described. With respect to frequent conflicting reports from different research groups, results reproducibly demonstrated by independent investigators are emphasized. Owing to many obstacles and limitations inherent in doing research on this noteworthy virus, the current knowledge is incomplete and the answers to many important questions are to be expected in the future.

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References
1.
Zhu N, Khoshnan A, Schneider R, Matsumoto M, Dennert G, Ware C . Hepatitis C virus core protein binds to the cytoplasmic domain of tumor necrosis factor (TNF) receptor 1 and enhances TNF-induced apoptosis. J Virol. 1998; 72(5):3691-7. PMC: 109590. DOI: 10.1128/JVI.72.5.3691-3697.1998. View

2.
Boyer J, Haenni A . Infectious transcripts and cDNA clones of RNA viruses. Virology. 1994; 198(2):415-26. DOI: 10.1006/viro.1994.1053. View

3.
Kurosaki M, Enomoto N, Marumo F, Sato C . Rapid sequence variation of the hypervariable region of hepatitis C virus during the course of chronic infection. Hepatology. 1993; 18(6):1293-9. View

4.
Owsianka A, Patel A . Hepatitis C virus core protein interacts with a human DEAD box protein DDX3. Virology. 1999; 257(2):330-40. DOI: 10.1006/viro.1999.9659. View

5.
Ferrari E, Fang J, Baroudy B, Lau J, Hong Z . Characterization of soluble hepatitis C virus RNA-dependent RNA polymerase expressed in Escherichia coli. J Virol. 1999; 73(2):1649-54. PMC: 103993. DOI: 10.1128/JVI.73.2.1649-1654.1999. View