CPF-DD is an inhibitor of infection by human immunodeficiency virus and other enveloped viruses in vitro

Virology. 1992 Jun;188(2):537-44. doi: 10.1016/0042-6822(92)90508-m.

Abstract

The initial step in the infection cycle of human immunodeficiency virus type 1 (HIV-1) involves binding of its surface glycoprotein gp 120 to the T lymphocyte CD4 antigen. CPF-DD is a low molecular weight inhibitor of HIV infectivity that inhibits gp 120 binding to CD4 in vitro (Finberg et al., Science 249, 287-291, 1990). We find, however, that the actions of CPF-DD are not limited to its ability to interfere with gp 120-CD4 binding; its predominant action is to remove the viral envelope from the underlying core. Subsequently the virions disintegrate. Most enveloped viruses tested were inhibited by CPF-DD, but the infectivity of noneneloped viruses was unaffected or only slightly reduced.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / pharmacology*
  • Benzyl Compounds / pharmacology*
  • CD4 Antigens / metabolism
  • Cell Survival / drug effects
  • Cells, Cultured
  • Dipeptides / pharmacology*
  • HIV Envelope Protein gp120 / metabolism
  • HIV Infections / prevention & control*
  • HIV-1 / drug effects*
  • HIV-1 / growth & development
  • Humans
  • In Vitro Techniques
  • Lentivirus / drug effects
  • Protein Binding / drug effects
  • Retroviridae / drug effects
  • Virion / drug effects*

Substances

  • Antiviral Agents
  • Benzyl Compounds
  • CD4 Antigens
  • Dipeptides
  • HIV Envelope Protein gp120
  • N-carbomethoxycarbonyl-prolyl-phenylalanyl-benzyl ester