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HIV-1 proteinase is required for synthesis of pro-viral DNA.

Abstract
HIV-1 proteinase activity is thought to occur primarily post-integration by cleaving the viral Gag and Gag-Pol polyproteins. Its role in the pre-integration stages of viral replication, however, has not been studied in detail. Here we report that a synthetic peptide analogue, UK-88,947, which is a specific inhibitor of purified HIV-1 proteinase, inhibits the processing of the viral polyproteins in cultures of HIV-1 infected cells and prevents the formation of mature, infectious virions. Analysis of DNA from HIV-1 infected cells treated with UK-88,947 showed that viral DNA synthesis was inhibited when the compound was added to cultures one hour before infection. Similar results were obtained when AZT was used. Neither HIV-1 reverse transcriptase or the replication of FIV are inhibited by UK-88,947.
AuthorsC Baboonian, A Dalgleish, L Bountiff, J Gross, S Oroszlan, G Rickett, C Smith-Burchnell, P Troke, J Merson
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 179 Issue 1 Pg. 17-24 (Aug 30 1991) ISSN: 0006-291X [Print] United States
PMID1652947 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • DNA, Viral
  • HIV Protease Inhibitors
  • Oligonucleotide Probes
  • Oligopeptides
  • Recombinant Proteins
  • UK 88947
  • Zidovudine
  • HIV Protease
Topics
  • Amino Acid Sequence
  • Base Sequence
  • Cell Line
  • DNA, Viral (biosynthesis, genetics)
  • HIV Protease (metabolism, pharmacology)
  • HIV Protease Inhibitors
  • HIV-1 (enzymology, genetics, physiology)
  • Humans
  • Immunodeficiency Virus, Feline (drug effects, physiology)
  • Molecular Sequence Data
  • Oligonucleotide Probes
  • Oligopeptides (pharmacology)
  • Proviruses (genetics, physiology)
  • Recombinant Proteins (metabolism)
  • Substrate Specificity
  • Virus Replication (drug effects)
  • Zidovudine (pharmacology)

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