scholarly journals All-atom molecular dynamics study of hepatitis B virus containing pregenome RNA in solution

Author(s):  
Kazushi Fujimoto ◽  
Youhei Yamaguchi ◽  
Ryo Urano ◽  
Wataru Shinoda ◽  
Tetsuya Ishikawa ◽  
...  

Immature hepatitis B virus (HBV) captures nucleotides in its capsid for reverse transcription. The nucleotides and nucleotide analogue drugs, which are triphosphorylated and negatively charged in the cell, approach the capsid via diffusion and are absorbed into it. In this study, we performed a long-time molecular dynamics (MD) calculation of the entire HBV capsid containing pregenome RNA to investigate the interactions between the capsid and negatively charged substances. Electric field analysis demonstrated that negatively charged substances can approach the HBV capsid by thermal motion, avoiding spikes. The substances then migrate all over the floor of the HBV capsid. Finally, they find pores through which they can pass through the HBV capsid shell. Free energy profiles were calculated along these pores for small ions to understand their permeability through the pores. Anions (Cl-) showed higher free energy barriers than cations (Na+ and K+) through all pores, and the permeation rate of Cl- was eight times slower than that of K+ or Na+. Furthermore, the ions were more stable in the capsid than in the bulk water. Thus, the HBV capsid exerts ion selectivity for uptake and provides an environment for ions, such as nucleotides and nucleotide analogue drugs, to be stabilized within the capsid.

2021 ◽  
Author(s):  
Lu Chen ◽  
Wen-Guang Liu ◽  
Fei Xiong ◽  
Chao Ma ◽  
Chen Sun ◽  
...  

HBV capsid protein (CP) plays a vital role in multiple life cycles of HBV and represents a novel anti-HBV target. Recently, a novel series of heteroaryldihydropyrimidine (HAPs) derivatives have been...


Viruses ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 738 ◽  
Author(s):  
Hugues de Rocquigny ◽  
Virgile Rat ◽  
Florentin Pastor ◽  
Jean Luc Darlix ◽  
Christophe Hourioux ◽  
...  

The morphogenesis of Hepatitis B Virus (HBV) viral particles is nucleated by the oligomerization of HBc protein molecules, resulting in the formation of an icosahedral capsid shell containing the replication-competent nucleoprotein complex made of the viral polymerase and the pre-genomic RNA (pgRNA). HBc is a phospho-protein containing two distinct domains acting together throughout the viral replication cycle. The N-terminal domain, (residues 1–140), shown to self-assemble, is linked by a short flexible domain to the basic C-terminal domain (residues 150–183) that interacts with nucleic acids (NAs). In addition, the C-terminal domain contains a series of phospho-acceptor residues that undergo partial phosphorylation and de-phosphorylation during virus replication. This highly dynamic process governs the homeostatic charge that is essential for capsid stability, pgRNA packaging and to expose the C-terminal domain at the surface of the particles for cell trafficking. In this review, we discuss the roles of the N-terminal and C-terminal domains of HBc protein during HBV morphogenesis, focusing on how the C-terminal domain phosphorylation dynamics regulate its interaction with nucleic acids throughout the assembly and maturation of HBV particles.


2014 ◽  
Vol 22 (1) ◽  
pp. 37-45 ◽  
Author(s):  
T. Shen ◽  
X. M. Yan ◽  
H .X. Liu ◽  
B. X. Zhang ◽  
L. Li ◽  
...  

2002 ◽  
Vol 36 ◽  
pp. 88 ◽  
Author(s):  
D. Colledge ◽  
T. Shaw ◽  
S. Bowden ◽  
S. Locarnini ◽  
S. Lewin ◽  
...  

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