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Seitz, S.* ; Habjanic, J. ; Schütz, A.K. ; Bartenschlager, R.*

The hepatitis B virus envelope proteins: Molecular gymnastics throughout the viral life cycle.

Annu. Rev. Virol. 7, 263-288 (2020)
Verlagsversion DOI PMC
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
New hepatitis B virions released from infected hepatocytes are the result of an intricate maturation process that starts with the formation of the nucleocapsid providing a confined space where the viral DNA genome is synthesized via reverse transcription. Virion assembly is finalized by the enclosure of the icosahedral nucleocapsid within a heterogeneous envelope. The latter contains integral membrane proteins of three sizes, collectively known as hepatitis B surface antigen, and adopts multiple conformations in the course of the viral life cycle. The nucleocapsid conformation depends on the reverse transcription status of the genome, which in turn controls nucleocapsid interaction with the envelope proteins for virus exit. In addition, after secretion the virions undergo a distinct maturation step during which a topological switch of the large envelope protein confers infectivity. Here we review molecular determinants for envelopment and models that postulate molecular signals encoded in the capsid scaffold conducive or adverse to the recruitment of envelope proteins.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Dane Particle ; Electron Microscopy ; Glycosylation ; Maturation Signal ; Membrane Protein ; Nucleocapsid ; Post-translational Modification ; Topological Switch ; Virion Maturation; Large Surface Protein; Amino-acid-sequence; Pre-s Domain; Immature Secretion Phenotype; Naturally-occurring Mutation; Precore Protein; Dane Particles; Core Protein; Transmembrane Topology; Dual Topology
Sprache englisch
Veröffentlichungsjahr 2020
HGF-Berichtsjahr 2020
ISSN (print) / ISBN 2327-056X
e-ISSN 2327-0578
Quellenangaben Band: 7, Heft: 1, Seiten: 263-288 Artikelnummer: , Supplement: ,
Verlag Annual Reviews
Verlagsort Palo Alto, California
Begutachtungsstatus Peer reviewed
POF Topic(s) 30203 - Molecular Targets and Therapies
Forschungsfeld(er) Enabling and Novel Technologies
PSP-Element(e) G-503000-001
Förderungen DFG, German Research Foundation
Deutsche Forschungsgemeinschaft (DFG, German Research foundation)
Scopus ID 85092332096
PubMed ID 32600157
Erfassungsdatum 2020-07-06