Purification and partial characterization of human immunodeficiency virus type 2 reverse transcriptase

AIDS Res Hum Retroviruses. 1989 Feb;5(1):51-60. doi: 10.1089/aid.1989.5.51.

Abstract

We have raised a rabbit monospecific antibody against a synthetic peptide derived from a sequence within the COOH-terminal portion of the reverse transcriptase (RT) of HIV-1. This sequence was also found to be conserved in the predicted amino acid sequence of HIV-2. The antibody, designated C2003, cross-reacted with HIV-2 RT on immunoblots of HIV-2 virus extract and directly inhibited HIV-2 RT activity. Fractionation of HIV-2 RT by immunoaffinity chromatography with C2003 antibody yielded a pair of viral proteins of 68 and 55 kD associated with both RT and RNAse H activities. Both proteins were found to be highly immunogenic, recognized by 11 of 11 human sera that previously tested positive for antibodies to HIV-2 antigens in immunoblot assays.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Antibodies, Monoclonal / immunology
  • Cell Line, Transformed
  • Cross Reactions
  • Endoribonucleases / isolation & purification
  • HIV Antibodies / immunology*
  • HIV-2 / enzymology*
  • HIV-2 / immunology
  • Immunoblotting
  • Molecular Sequence Data
  • RNA-Directed DNA Polymerase / isolation & purification*
  • Ribonuclease H

Substances

  • Antibodies, Monoclonal
  • HIV Antibodies
  • RNA-Directed DNA Polymerase
  • Endoribonucleases
  • Ribonuclease H