Characterization of Fusion Determinants Points to the Involvement of Three Discrete Regions of Both E1 and E2 Glycoproteins in the Membrane Fusion Process of Hepatitis C Virus
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Receptor complementation and mutagenesis reveal SR-BI as an essential HCV entry factor and functionally imply its intra- and extra-cellular domainsRecent advances in understanding hepatitis CRoles of lipoprotein receptors in the entry of hepatitis C virusImpact of lipids and lipoproteins on hepatitis C virus infection and virus neutralizationThe hepatitis C virus glycan shield and evasion of the humoral immune responseIdentification of a novel drug lead that inhibits HCV infection and cell-to-cell transmission by targeting the HCV E2 glycoproteinDissecting the role of putative CD81 binding regions of E2 in mediating HCV entry: Putative CD81 binding region 1 is not involved in CD81 bindingCD81 and Claudin 1 Coreceptor Association: Role in Hepatitis C Virus EntryInteraction of the Most Membranotropic Region of the HCV E2 Envelope Glycoprotein with Membranes. Biophysical CharacterizationStructures and Mechanisms of Viral Membrane Fusion Proteins: Multiple Variations on a Common ThemeThe Tight Junction-Associated Protein Occludin Is Required for a Postbinding Step in Hepatitis C Virus Entry and InfectionLow pH-dependent Hepatitis C Virus Membrane Fusion Depends on E2 Integrity, Target Lipid Composition, and Density of Virus ParticlesA computational approach identifies two regions of Hepatitis C Virus E1 protein as interacting domains involved in viral fusion processHepatitis C Virus NS2 Protein Contributes to Virus Particle Assembly via Opposing Epistatic Interactions with the E1-E2 Glycoprotein and NS3-NS4A Enzyme ComplexesMutagenesis of the fusion peptide-like domain of hepatitis C virus E1 glycoprotein: involvement in cell fusion and virus entryMutational analysis of the hepatitis C virus E1 glycoprotein in retroviral pseudoparticles and cell-culture-derived H77/JFH1 chimeric infectious virus particlesThe Disulfide Bonds in Glycoprotein E2 of Hepatitis C Virus Reveal the Tertiary Organization of the MoleculeIdentification of New Functional Regions in Hepatitis C Virus Envelope Glycoprotein E2Structure of the core ectodomain of the hepatitis C virus envelope glycoprotein 2A novel small molecule inhibitor of hepatitis C virus entryMechanism of inhibition of enveloped virus membrane fusion by the antiviral drug arbidolHuman monoclonal antibodies to a novel cluster of conformational epitopes on HCV E2 with resistance to neutralization escape in a genotype 2a isolateFusogenic properties of the ectodomains of hepatitis C virus envelope proteins.Unexpected structural features of the hepatitis C virus envelope protein 2 ectodomain.Capitalizing on knowledge of hepatitis C virus neutralizing epitopes for rational vaccine designThe missing pieces of the HCV entry puzzle.Hepatitis C virus experimental model systems and antiviral drug research.Identification of conserved residues in hepatitis C virus envelope glycoprotein E2 that modulate virus dependence on CD81 and SRB1 entry factors.The Humoral Immune Response to HCV: Understanding is Key to Vaccine Development.Designing and Development of a DNA Vaccine Based On Structural Proteins of Hepatitis C VirusPotential treatment options and future research to increase hepatitis C virus treatment response ratePhenothiazines inhibit hepatitis C virus entry, likely by increasing the fluidity of cholesterol-rich membranes.Functional characterization of nuclear localization and export signals in hepatitis C virus proteins and their role in the membranous web.Hepatitis C virus life cycle and lipid metabolismUp-regulation of the ATP-binding cassette transporter A1 inhibits hepatitis C virus infection.Hepatitis C virus is primed by CD81 protein for low pH-dependent fusionHepatitis C virus (HCV) envelope glycoproteins E1 and E2 contain reduced cysteine residues essential for virus entry.Hepatitis C virus E1 envelope glycoprotein interacts with apolipoproteins in facilitating entry into hepatocytes.Flunarizine prevents hepatitis C virus membrane fusion in a genotype-dependent manner by targeting the potential fusion peptide within E1.New Insights into the Understanding of Hepatitis C Virus Entry and Cell-to-Cell Transmission by Using the Ionophore Monensin A.
P2860
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P2860
Characterization of Fusion Determinants Points to the Involvement of Three Discrete Regions of Both E1 and E2 Glycoproteins in the Membrane Fusion Process of Hepatitis C Virus
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@ast
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@en
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@nl
type
label
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@ast
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@en
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@nl
prefLabel
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@ast
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@en
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@nl
P2093
P2860
P50
P356
P1433
P1476
Characterization of Fusion Det ...... n Process of Hepatitis C Virus
@en
P2093
Eve-Isabelle Pécheur
Jennifer Molle
Judith Fresquet
Marlène Dreux
Peggy Donot
Romuald Corbau
P2860
P304
P356
10.1128/JVI.02642-06
P577
2007-08-01T00:00:00Z