Document 3294 DOCN M94A3294 TI The expression of gag-pol and gag-pol-env sequences of HIV-1 by recombinant vaccinia viruses. DT 9412 AU Grigoriev VB; Gibadulin RA; Liendeman LF; Sazykin AY; D.I. Ivanovsky Institute of Virology, Rus. Acad. Med. Sci.; Moscow. SO Int Conf AIDS. 1994 Aug 7-12;10(1):109 (abstract no. PA0054). Unique Identifier : AIDSLINE ICA10/94369281 AB OBJECTIVE: To study assembly of virus like particle (VLP) in process of expression of gag-pol and gag-pol-env sequences we constructed recombinant vaccinia virus (VV) strains (RVV). METHODS: RVVs were constructed by insertion of the gag-pol and gag-pol-env sequences into VV and termed as RV-1 and RV-2. The expression of HIV-1 proteins by RVVs was analyzed by immunoblotting and electron microscopy. (EM) RESULTS: RV-1 synthesized p55, p41 and p24 polypeptides in cells. P17 was presented in minor quantaties. This strain didn't form VLP in CV-1 and Hep-2 cell cultures. RV-2 synthesized p160gag, p55gag, 3-4 proteins of p50-53gag, as well as p41gag ahd p17gag. P24 was present in minor quantaties. In CV-1 cells gag-proteins didn t form VLP, however in Hep-2 cells muture and immuture VLP can be found by EM. In the cells are co-infected with RV-1 and RV-2 all above mentioned proteins and VLP were found. CONCLUSION: The formation of VLP by RV-2 depends on type of cell culture and level of synthesis of p17. In the cells are co-infected with two strains, each strain proteins are processed separetely from each other. DE Cell Line Gene Expression Gene Products, env/BIOSYNTHESIS/GENETICS Gene Products, gag/BIOSYNTHESIS/GENETICS Gene Products, pol/BIOSYNTHESIS/GENETICS *Genes, env *Genes, gag *Genes, pol Human HIV Antigens/BIOSYNTHESIS/GENETICS HIV-1/GROWTH & DEVELOPMENT/*GENETICS/METABOLISM Recombination, Genetic Vaccinia Virus/GENETICS MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).