Literature DB >> 23966388

Maturation-associated destabilization of hepatitis B virus nucleocapsid.

Xiuji Cui1, Laurie Ludgate, Xiaojun Ning, Jianming Hu.   

Abstract

The mature nucleocapsid (NC) of hepatitis B virus containing the relaxed circular (RC) DNA genome can be secreted extracellularly as virions after envelopment with the viral surface proteins or, alternatively, can be disassembled to release RC DNA (i.e., uncoating) into the host cell nucleus to form the covalently closed circular (CCC) DNA, which sustains viral replication and persistence. In contrast, immature NCs containing the viral single-stranded DNA or the pregenomic RNA are incompetent for either envelopment or uncoating. Little is currently known about how mature NCs, and not the immature ones, are specifically selected for these processes. Here, we have carried out a biochemical analysis of the different NC populations upon their separation through sucrose gradient centrifugation. We have found that the maturation of NCs is associated with their destabilization, manifested as increased protease and nuclease sensitivity, altered sedimentation during sucrose gradient centrifugation, and retarded mobility during native agarose gel electrophoresis. Also, three distinct populations of intracellular mature NCs could be differentiated based on these characteristics. Furthermore, mature NCs generated in vitro under cell-free conditions acquired similar properties. These results have thus revealed significant structural changes associated with NC maturation that likely play a role in the selective uncoating of the mature NC for CCC DNA formation and/or its preferential envelopment for virion secretion.

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Year:  2013        PMID: 23966388      PMCID: PMC3807348          DOI: 10.1128/JVI.01912-13

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  61 in total

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2.  Inducible expression of human hepatitis B virus (HBV) in stably transfected hepatoblastoma cells: a novel system for screening potential inhibitors of HBV replication.

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3.  Reverse transcription-associated dephosphorylation of hepadnavirus nucleocapsids.

Authors:  David H Perlman; Eric A Berg; Peter B O'connor; Catherine E Costello; Jianming Hu
Journal:  Proc Natl Acad Sci U S A       Date:  2005-06-10       Impact factor: 11.205

4.  Roles of the three major phosphorylation sites of hepatitis B virus core protein in viral replication.

Authors:  Y T Lan; J Li; W Liao; J Ou
Journal:  Virology       Date:  1999-07-05       Impact factor: 3.616

5.  Parvovirus uncoating in vitro reveals a mechanism of DNA release without capsid disassembly and striking differences in encapsidated DNA stability.

Authors:  Carlos Ros; Claudia Baltzer; Bernhard Mani; Christoph Kempf
Journal:  Virology       Date:  2005-10-20       Impact factor: 3.616

6.  Hepatitis B virus nucleocapsids formed by carboxy-terminally mutated core proteins contain spliced viral genomes but lack full-size DNA.

Authors:  Josef Köck; Michael Nassal; Karl Deres; Hubert E Blum; Fritz von Weizsäcker
Journal:  J Virol       Date:  2004-12       Impact factor: 5.103

7.  A conserved linear B-cell epitope at the N-terminal region of woodchuck hepatitis virus core protein (WHcAg).

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8.  Cyclin-dependent kinase 2 phosphorylates s/t-p sites in the hepadnavirus core protein C-terminal domain and is incorporated into viral capsids.

Authors:  Laurie Ludgate; Xiaojun Ning; David H Nguyen; Christina Adams; Laura Mentzer; Jianming Hu
Journal:  J Virol       Date:  2012-09-05       Impact factor: 5.103

9.  Requirement of heat shock protein 90 for human hepatitis B virus reverse transcriptase function.

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10.  Phosphorylation-dependent binding of hepatitis B virus core particles to the nuclear pore complex.

Authors:  M Kann; B Sodeik; A Vlachou; W H Gerlich; A Helenius
Journal:  J Cell Biol       Date:  1999-04-05       Impact factor: 10.539

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  45 in total

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Authors:  Jun Luo; Xiuji Cui; Lu Gao; Jianming Hu
Journal:  J Virol       Date:  2017-08-10       Impact factor: 5.103

Review 2.  Metabolism and function of hepatitis B virus cccDNA: Implications for the development of cccDNA-targeting antiviral therapeutics.

Authors:  Ju-Tao Guo; Haitao Guo
Journal:  Antiviral Res       Date:  2015-08-10       Impact factor: 5.970

3.  Local Stabilization of Subunit-Subunit Contacts Causes Global Destabilization of Hepatitis B Virus Capsids.

Authors:  Christopher John Schlicksup; Patrick Laughlin; Steven Dunkelbarger; Joseph Che-Yen Wang; Adam Zlotnick
Journal:  ACS Chem Biol       Date:  2020-05-19       Impact factor: 5.100

4.  The interface between hepatitis B virus capsid proteins affects self-assembly, pregenomic RNA packaging, and reverse transcription.

Authors:  Zhenning Tan; Karolyn Pionek; Nuruddin Unchwaniwala; Megan L Maguire; Daniel D Loeb; Adam Zlotnick
Journal:  J Virol       Date:  2015-01-07       Impact factor: 5.103

5.  A Thermodynamic Model for Genome Packaging in Hepatitis B Virus.

Authors:  Jehoon Kim; Jianzhong Wu
Journal:  Biophys J       Date:  2015-10-20       Impact factor: 4.033

Review 6.  The Structural Biology of Hepatitis B Virus: Form and Function.

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Journal:  Annu Rev Virol       Date:  2016-08-01       Impact factor: 10.431

7.  Unveiling the roles of HBV polymerase for new antiviral strategies.

Authors:  Daniel N Clark; Jianming Hu
Journal:  Future Virol       Date:  2015       Impact factor: 1.831

Review 8.  Hepatitis B virus cccDNA: Formation, regulation and therapeutic potential.

Authors:  Yuchen Xia; Haitao Guo
Journal:  Antiviral Res       Date:  2020-05-22       Impact factor: 5.970

Review 9.  Revisiting Hepatitis B Virus: Challenges of Curative Therapies.

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Journal:  J Virol       Date:  2019-09-30       Impact factor: 5.103

10.  Viral DNA-Dependent Induction of Innate Immune Response to Hepatitis B Virus in Immortalized Mouse Hepatocytes.

Authors:  Xiuji Cui; Daniel N Clark; Kuancheng Liu; Xiao-Dong Xu; Ju-Tao Guo; Jianming Hu
Journal:  J Virol       Date:  2015-10-21       Impact factor: 5.103

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