Document 0368 DOCN M9610368 TI Analysis of cross reactivity of retrovirus proteases using a vaccinia virus-T7 RNA polymerase-based expression system. DT 9601 AU Luukkonen BG; Tan W; Fenyo EM; Schwartz S; Microbiology and Tumorbiology Center, Karolinska Institute,; Stockholm, Sweden. SO J Gen Virol. 1995 Sep;76 ( Pt 9):2169-80. Unique Identifier : AIDSLINE MED/96005038 AB We have used the vaccinia virus-T7 RNA polymerase-based expression system for studies on the activity of proteases from various retroviruses on homologous and heterologous Gag polyproteins in eukaryotic cells. Proteases from human immunodeficiency virus (HIV) types 1 and 2, equine infectious anaemia virus, human T cell leukaemia virus type 1 and human spumavirus were produced and were shown to cleave their cognate Gag substrates produced in trans. Analysis of cross reactivity revealed that lentivirus proteases cleaved only lentivirus Gag proteins and oncovirus proteases acted primarily on oncovirus Gag proteins. The HIV-2 protease cleaved the HIV-1 Gag precursor almost as efficiently as HIV-1 protease. Expression of the 5' end of the human spumavirus pol gene revealed that it encodes a functional protease that acts specifically on the human spumavirus Gag polyprotein. This assay will allow further investigation on the activity and specificity of retrovirus proteases in eukaryotic cells. DE Amino Acid Sequence Animal Base Sequence Gene Products, gag/*METABOLISM Gene Products, pol Genetic Vectors Hela Cells Human HIV/ENZYMOLOGY/GENETICS HTLV-I/ENZYMOLOGY/GENETICS Infectious Anemia Virus, Equine/ENZYMOLOGY/GENETICS Molecular Sequence Data Peptide Peptidohydrolases/GENETICS/*METABOLISM Recombinant Fusion Proteins/GENETICS/METABOLISM Retroviridae/*ENZYMOLOGY/GENETICS RNA Polymerases/GENETICS Spumavirus/ENZYMOLOGY/GENETICS Substrate Specificity Support, Non-U.S. Gov't Vaccinia Virus/*GENETICS JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).