Detection of inhibition of HIV-1 protease activity by an enzyme-linked immunosorbent assay (ELISA)

J Immunol Methods. 1993 May 26;161(2):151-5. doi: 10.1016/0022-1759(93)90290-n.

Abstract

An ELISA is described for the detection of HIV-1 protease activity using an immobilized gag-related polyprotein as substrate. Proteolytic activity was demonstrated with either bacterial lysates expressing HIV-1 protease or purified protease. No cleavage was observed with a protein preparation from control bacteria not expressing HIV-1 protease. Under these conditions the aspartyl-type protease inhibitor, pepstatin A, was found to inhibit HIV-1 protease cleavage by > 90% at a concentration of 0.1 mM. This assay may be a useful tool for the study of both synthetic and natural inhibitors of HIV-1 protease.

MeSH terms

  • Enzyme-Linked Immunosorbent Assay*
  • HIV Core Protein p24 / metabolism
  • HIV Envelope Protein gp41 / metabolism
  • HIV Protease Inhibitors / analysis*
  • HIV-1 / enzymology*
  • Recombinant Fusion Proteins / metabolism

Substances

  • HIV Core Protein p24
  • HIV Envelope Protein gp41
  • HIV Protease Inhibitors
  • Recombinant Fusion Proteins