Affinity purification of the HIV-1 protease

Biochem Biophys Res Commun. 1989 Nov 15;164(3):955-60. doi: 10.1016/0006-291x(89)91762-2.

Abstract

An inhibitor of the HIV-1 protease has been employed in the generation of a resin which allows the rapid purification of this enzyme. A peptide substrate analogue, H2N-Ser-Gln-Asn-(Phe-psi[CH2N]-Pro)-Ile-Val-Gln-OH, was coupled to agarose resin. The HIV-1 protease was expressed in E. coli and the supernatant from lysed cells was passed through the affinity resin. Active HIV-1 protease was then eluted with a buffer change to pH 10 and 2 M NaCl. Final purification to a homogeneous preparation, capable of crystallization, was achieved with hydrophobic interaction chromatography. Solutions containing HIV-1 protease bound to competitive inhibitors do not bind to the column.

MeSH terms

  • Amino Acid Sequence
  • Chromatography, Affinity / methods
  • Chromatography, Gel
  • Cloning, Molecular
  • Electrophoresis, Polyacrylamide Gel
  • Endopeptidases / genetics
  • Endopeptidases / isolation & purification*
  • Endopeptidases / metabolism
  • Escherichia coli / genetics
  • HIV Protease
  • HIV-1 / enzymology*
  • Kinetics
  • Ligands
  • Molecular Sequence Data
  • Molecular Weight
  • Oligopeptides / chemical synthesis
  • Oligopeptides / pharmacology
  • Plasmids

Substances

  • Ligands
  • Oligopeptides
  • Endopeptidases
  • HIV Protease