Maturation inhibitors facilitate virus assembly and release of HIV-1 capsid P224 mutant

Virology. 2018 Aug:521:44-50. doi: 10.1016/j.virol.2018.05.024. Epub 2018 Jun 4.

Abstract

HIV-1 Maturation inhibitors (MIs) bind to the C-terminal domain of capsid protein (CA-CTD) and spacer peptide 1 (SP1) in HIV-1 Gag and inhibit the CA-SP1 cleavage by stabilizing the immature Gag. The β-turn motif, GVGGP in the HIV CA-CTD (residues 220-224) is one of the key determinants of HIV Gag assembly. In the present study, we mutated each residue of HIV-1 β-turn motif to alanine and observed complete inhibition of virus release of all mutants. This defect in virus release was rescued in the presence of maturation inhibitors; BVM and PF-46396 for P224A mutant. To our knowledge, this is the first report of identification of BVM and PF-46396-dependent capsid mutant. Our results highlight the importance of the core β-turn motif residues in immature virus assembly and suggest that the presence of MIs enhances Gag membrane binding and multimerization thereby restoring virus release of HIV Gag P224 mutant.

Keywords: Gag assembly; HIV; Maturation inhibitors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs / genetics
  • Anti-HIV Agents / pharmacology*
  • Capsid Proteins / antagonists & inhibitors
  • Capsid Proteins / genetics*
  • Cell Line
  • Genes, gag
  • HIV-1 / chemistry
  • HIV-1 / drug effects
  • HIV-1 / genetics*
  • Humans
  • Mutation*
  • T-Lymphocytes / virology
  • Virus Assembly / genetics
  • gag Gene Products, Human Immunodeficiency Virus / metabolism*

Substances

  • Anti-HIV Agents
  • Capsid Proteins
  • gag Gene Products, Human Immunodeficiency Virus