Identification of a Class of HCV Inhibitors Directed Against the Nonstructural Protein NS4B

被引:53
作者
Cho, Nam-Joon [1 ,2 ]
Dvory-Sobol, Hadas [1 ]
Lee, Choongho [1 ]
Cho, Sang-Joon [3 ]
Bryson, Paul [1 ]
Masek, Marilyn [1 ]
Elazar, Menashe [1 ]
Frank, Curtis W. [2 ]
Glenn, Jeffrey S. [1 ,4 ]
机构
[1] Stanford Univ, Sch Med, Div Gastroenterol & Hepatol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[3] Pk Syst Inc, Suwon 443270, South Korea
[4] Vet Adm Med Ctr, Palo Alto, CA 94304 USA
关键词
HEPATITIS-C-VIRUS; RNA REPLICATION; ENDOPLASMIC-RETICULUM; MEMBRANE ASSOCIATION; AMPHIPATHIC HELIX; VIRAL REPLICATION; INFECTION; COMPLEX; NS5A; LOCALIZATION;
D O I
10.1126/scitranslmed.3000331
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:8
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