نتایج جستجو برای: NS5B polymerase

تعداد نتایج: 128417  

Journal: :Journal of virology 2002
Q May Wang Michelle A Hockman Kirk Staschke Robert B Johnson Katharine A Case Jirong Lu Steve Parsons Faming Zhang Radhakrishnan Rathnachalam Karla Kirkegaard Joseph M Colacino

The NS5B RNA-dependent RNA polymerase encoded by hepatitis C virus (HCV) plays a key role in viral replication. Reported here is evidence that HCV NS5B polymerase acts as a functional oligomer. Oligomerization of HCV NS5B protein was demonstrated by gel filtration, chemical cross-linking, temperature sensitivity, and yeast cell two-hybrid analysis. Mutagenesis studies showed that the C-terminal...

2016
Marleen H M Hessel Adam F Cohen Robert Rissmann

After entering hepatocytes, the viral genome of the hepatitis C virus (HCV) is translated into a single polypeptide. This polypeptide is subsequently cleaved into viral proteins, including non-structural (NS) proteins NS3, NS4A, NS5B and NS5B RNA dependent RNA polymerase (Figure 1) [3, 4]. These viral proteins are essential for viral replication and assembly making them significant targets for ...

Journal: :Nucleic acids research 2004
Ginette McKercher Pierre L Beaulieu Daniel Lamarre Steven LaPlante Sylvain Lefebvre Charles Pellerin Louise Thauvette George Kukolj

The interaction of the hepatitis C virus (HCV) RNA-dependent RNA polymerase with RNA substrate is incompletely defined. We have characterized the activities of the HCV NS5B polymerase, modified by different deletions and affinity tags, with a routinely used homopolymeric substrate, and established apparent affinities of the various NS5B constructs both for the NTP and the template/primer substr...

Journal: :The Journal of biological chemistry 2009
Julie Qi Hang Yanli Yang Seth F Harris Vincent Leveque Hannah J Whittington Sonal Rajyaguru Gloria Ao-Ieong Matthew F McCown April Wong Anthony M Giannetti Sophie Le Pogam Francisco Talamás Nick Cammack Isabel Nájera Klaus Klumpp

The binding affinity of four palm and thumb site representative non-nucleoside inhibitors (NNIs) of HCV polymerase NS5B to wild-type and resistant NS5B polymerase proteins was determined, and the influence of RNA binding on NNI binding affinity was investigated. NNIs with high binding affinity potently inhibited HCV RNA polymerase activity and replicon replication. Among the compounds tested, H...

Journal: :Intervirology 2015
Sarah Aherfi Olga Glazunova Patrick Borentain Daniele Botta-Fridlund Laurent Chiche Sylvie Bregigeon Anne Motte Catherine Tamalet Philippe Colson

The rate of eradication of chronic hepatitis C considerably increases with direct-acting antiviral agents, particularly hepatitis C virus (HCV) polymerase inhibitors. While implementing full-length HCV NS5B polymerase sequencing in our clinical microbiology laboratory, we identified atypical HCV sequences, classified as subtype 2l, from 2 patients. HCV-2l NS5B polymerase sequences were detected...

2012
Christy M. Hebner Bin Han Katherine M. Brendza Michelle Nash Maisoun Sulfab Yang Tian Magdeleine Hung Wanchi Fung Randall W. Vivian James Trenkle James Taylor Kyla Bjornson Steven Bondy Xiaohong Liu John Link Johan Neyts Roman Sakowicz Weidong Zhong Hengli Tang Uli Schmitz

Tegobuvir (TGV) is a novel non-nucleoside inhibitor (NNI) of HCV RNA replication with demonstrated antiviral activity in patients with genotype 1 chronic HCV infection. The mechanism of action of TGV has not been clearly defined despite the identification of resistance mutations mapping to the NS5B polymerase region. TGV does not inhibit NS5B enzymatic activity in biochemical assays in vitro, s...

Journal: :The Journal of biological chemistry 2012
Claire Rosnoblet Bernd Fritzinger Dominique Legrand Hélène Launay Jean-Michel Wieruszeski Guy Lippens Xavier Hanoulle

Nonstructural protein 5B (NS5B) is essential for hepatitis C virus (HCV) replication as it carries the viral RNA-dependent RNA polymerase enzymatic activity. HCV replication occurs in a membrane-associated multiprotein complex in which HCV NS5A and host cyclophilin A (CypA) have been shown to be present together with the viral polymerase. We used NMR spectroscopy to perform a per residue level ...

2011
Pilar Clemente-Casares Alberto J. López-Jiménez Itxaso Bellón-Echeverría José Antonio Encinar Elisa Martínez-Alfaro Ricardo Pérez-Flores Antonio Mas

Hepatitis C virus (HCV) shows a great geographical diversity reflected in the high number of circulating genotypes and subtypes. The response to HCV treatment is genotype specific, with the predominant genotype 1 showing the lowest rate of sustained virological response. Virally encoded enzymes are candidate targets for intervention. In particular, promising antiviral molecules are being develo...

2011
C. T. Ranjith-Kumar Yahong Wen Nielson Baxter Kanchan Bhardwaj C. Cheng Kao

RNA synthesis by the genotype 1b hepatitis C virus (HCV) polymerase (NS5B) transiently expressed in Human embryonic kidney 293T cells or liver hepatocytes was found to robustly stimulate RIG-I-dependent luciferase production from the interferon β promoter in the absence of exogenously provided ligand. This cell-based assay, henceforth named the 5BR assay, could be used to examine HCV polymerase...

2016
Yu Wei Jinlong Li Jie Qing Mingjie Huang Ming Wu Fenghua Gao Dongmei Li Zhangyong Hong Lingbao Kong Weiqiang Huang Jianping Lin Giovanni Maga

The NS5B polymerase is one of the most attractive targets for developing new drugs to block Hepatitis C virus (HCV) infection. We describe the discovery of novel potent HCV NS5B polymerase inhibitors by employing a virtual screening (VS) approach, which is based on random forest (RB-VS), e-pharmacophore (PB-VS), and docking (DB-VS) methods. In the RB-VS stage, after feature selection, a model w...

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