A heteroaryldihydropyrimidine activates and can misdirect hepatitis B virus capsid assembly

Proc Natl Acad Sci U S A. 2005 Jun 7;102(23):8138-43. doi: 10.1073/pnas.0409732102. Epub 2005 May 31.

Abstract

Heteroaryldihydropyrimidines (HAPs) are a new class of antivirals inhibiting production of hepatitis B virus (HBV) virions in tissue culture. Here, we examine the effect of a representative HAP molecule, methyl 4-(2-chloro-4-fluorophenyl)-6-methyl-2-(pyridin-2-yl)-1,4-dihydropyrimidine-5-carboxylate (HAP-1), on the in vitro assembly of HBV capsid protein (Cp). HAP-1 enhances the rate and extent of Cp assembly over a broad concentration range. Aberrant particles, dominated by hexagonal arrays of Cp, were observed from assembly reactions with high HAP-1 concentrations. HAP-1 also led to dissociation of metastable HBV capsids, overcoming a kinetic barrier to dissociation by scavenging Cp and redirecting its assembly into hexamer-rich structures. Thus, HAP drugs act as allosteric effectors that induce an assembly-active state and, at high concentration, preferentially stabilize noncapsid polymers of Cp. HAP compounds may have multiple effects in vivo stemming from inappropriate assembly of Cp. These results show that activating and deregulating virus assembly may be a powerful general approach for antiviral therapeutics.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Allosteric Regulation / drug effects
  • Capsid / chemistry
  • Capsid / drug effects*
  • Capsid / metabolism*
  • Capsid / ultrastructure
  • Dimerization
  • Hepatitis B virus / chemistry
  • Hepatitis B virus / drug effects*
  • Hepatitis B virus / growth & development*
  • Hepatitis B virus / ultrastructure
  • Kinetics
  • Models, Molecular
  • Protein Structure, Quaternary / drug effects
  • Pyridines / pharmacology*
  • Pyrimidines / pharmacology*
  • Virus Assembly / drug effects*

Substances

  • Pyridines
  • Pyrimidines
  • methyl 4-(2-chloro-4-fluorophenyl)-6-methyl-2-(pyridin-2-yl)-1,4-dihydropyrimidine-5-carboxylate