| Literature DB >> 20371471 |
Nam-Joon Cho1, Hadas Dvory-Sobol, Choongho Lee, Sang-Joon Cho, Paul Bryson, Marilyn Masek, Menashe Elazar, Curtis W Frank, Jeffrey S Glenn.
Abstract
New classes of drugs are needed to combat hepatitis C virus (HCV), an important worldwide cause of liver disease. We describe an activity of a key domain, an amphipathic helix we termed 4BAH2, within a specific HCV nonstructural protein, NS4B. In addition to its proposed role in viral replication, we validate 4BAH2 as essential for HCV genome replication and identify first-generation small-molecule inhibitors of 4BAH2 that specifically prevent HCV replication within cells. Mechanistic studies reveal that the inhibitors target 4BAH2 function by preventing either 4BAH2 oligomerization or 4BAH2 membrane association. 4BAH2 inhibitors represent an additional class of compounds with potential to effectively treat HCV.Entities:
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Year: 2010 PMID: 20371471 PMCID: PMC3025298 DOI: 10.1126/scitranslmed.3000331
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956