Anna Albecka
Identification of new functional regions in hepatitis C virus envelope glycoprotein E2
Albecka, Anna; Montserret, Roland; Krey, Thomas; Tarr, Alexander W.; Diesis, Eric; Ball, Jonathan K.; Descamps, Véronique; Duverlie, Gilles; Rey, Felix; Penin, François; Dubuisson, Jean
Authors
Roland Montserret
Thomas Krey
Dr Alexander Tarr Alex.Tarr@nottingham.ac.uk
ASSOCIATE PROFESSOR
Eric Diesis
Jonathan K. Ball
Véronique Descamps
Gilles Duverlie
Felix Rey
François Penin
Jean Dubuisson
Abstract
Little is known about the structure of the envelope glycoproteins of hepatitis C virus (HCV). To identify new regions essential for the function of these glycoproteins, we generated HCV pseudoparticles (HCVpp) containing HCV envelope glycoproteins, E1 and E2, from different genotypes in order to detect intergenotypic incompatibilities between these two proteins. Several genotype combinations were nonfunctional for HCV entry. Of interest, a combination of E1 from genotype 2a and E2 from genotype 1a was nonfunctional in the HCVpp system. We therefore used this nonfunctional complex and the recently described structural model of E2 to identify new functional regions in E2 by exchanging protein regions between these two genotypes. The functionality of these chimeric envelope proteins in the HCVpp system and/or the cell-cultured infectious virus (HCVcc) was analyzed. We showed that the intergenotypic variable region (IgVR), hypervariable region 2 (HVR2), and another segment in domain II play a role in E1E2 assembly. We also demonstrated intradomain interactions within domain I. Importantly, we also identified a segment (amino acids [aa] 705 to 715 [segment 705-715]) in the stem region of E2, which is essential for HCVcc entry. Circular dichroism and nuclear magnetic resonance structural analyses of the synthetic peptide E2-SC containing this segment revealed the presence of a central amphipathic helix, which likely folds upon membrane binding. Due to its location in the stem region, segment 705-715 is likely involved in the reorganization of the glycoprotein complexes taking place during the fusion process. In conclusion, our study highlights new functional and structural regions in HCV envelope glycoprotein E2. Copyright © 2011, American Society for Microbiology. All Rights Reserved.
Citation
Albecka, A., Montserret, R., Krey, T., Tarr, A. W., Diesis, E., Ball, J. K., Descamps, V., Duverlie, G., Rey, F., Penin, F., & Dubuisson, J. (2011). Identification of new functional regions in hepatitis C virus envelope glycoprotein E2. Journal of Virology, 85(4), 1777-1792. https://doi.org/10.1128/JVI.02170-10
Journal Article Type | Article |
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Acceptance Date | Nov 29, 2010 |
Online Publication Date | Jan 20, 2011 |
Publication Date | Feb 1, 2011 |
Deposit Date | Nov 9, 2022 |
Journal | Journal of Virology |
Print ISSN | 0022-538X |
Electronic ISSN | 1098-5514 |
Publisher | American Society for Microbiology |
Peer Reviewed | Peer Reviewed |
Volume | 85 |
Issue | 4 |
Pages | 1777-1792 |
DOI | https://doi.org/10.1128/JVI.02170-10 |
Public URL | https://nottingham-repository.worktribe.com/output/3129530 |
Publisher URL | https://journals.asm.org/doi/10.1128/JVI.02170-10 |