Analysis of HIV particle formation using transient expression of subviral constructs in mammalian cells

K Mergener1, M Fäcke, R Welker

  • 1Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

Virology
|January 1, 1992
PubMed

Insights

This study shows that human immunodeficiency virus (HIV) gag and pol gene expression in mammalian cells can produce retrovirus-like particles. Particle release depends on myristoylation, and HIV protease activity influences budding and cell toxicity.

Area of Science:

  • Virology
  • Molecular Biology
  • Cell Biology

Background:

  • Understanding human immunodeficiency virus (HIV) assembly is crucial for developing antiviral therapies.
  • The gag and pol genes encode essential viral structural proteins and enzymes involved in replication.
  • The role of viral protease (PR) and myristoylation in HIV particle formation requires further elucidation.

Purpose of the Study:

  • To investigate the expression of human immunodeficiency virus (HIV) type 1 gag and pol genes in mammalian cells.
  • To characterize the formation and release of retrovirus-like particles.
  • To determine the impact of mutations and proteinase activity on particle production and morphology.

Main Methods:

  • Transient expression of HIV gag and pol gene segments in mammalian cells.
  • Detection of protein expression using indirect immunofluorescence and Western blotting.
  • Analysis of particle release, density, composition, and morphology via sucrose density gradients, reverse transcriptase (RT) activity assays, and electron microscopy.

Main Results:

  • Expression of gag and pol genes resulted in the release of particles containing processed gag proteins, reverse transcriptase (RT), and RNA.
  • Particle production was independent of pol or active HIV proteinase (PR), but PR deficiency led to uncleaved proteins and vacuolar budding.
  • Myristoylation is essential for particle release, and PR overexpression caused cytotoxicity and aberrant particle morphology, while PR active site mutations restored release.

Conclusions:

  • HIV gag and pol gene expression can lead to the formation and release of immature retrovirus-like particles.
  • Myristoylation is critical for efficient particle release.
  • HIV proteinase activity plays a complex role, influencing both polyprotein processing and particle release dynamics, with overexpression leading to toxicity.

Related Concept Videos