REACTION OF P55 AND P48GAG POLYPROTEIN PR ECURSORS WITH P160GAG-POL DURING FORMATION OF HIV-1 VIRUS-LIKE PARTICLES BY RECOMBINANT VACCINIA VIRUS-STRAINS
Sn. Iordansky et al., REACTION OF P55 AND P48GAG POLYPROTEIN PR ECURSORS WITH P160GAG-POL DURING FORMATION OF HIV-1 VIRUS-LIKE PARTICLES BY RECOMBINANT VACCINIA VIRUS-STRAINS, Voprosy virusologii, 42(5), 1997, pp. 205-208
The polypeptide composition of HIV-1 virus-like particles produced by
CV-1 cells during mono- and coinfection with recombinant vaccinia viru
s (rVV) strains containing the whole (p55) and carboxyterminal truncat
ed (p48) gag genes and gag-pol sequence is studied. In monoinfection b
oth the gag-strains actively produced virus-like particles consisting
of non-processed p55Gag and p48Gag polyprotein without p6 domain. In c
ase of a coinfection of the cells with one of these strains and the rV
V producing p160Gag-Pol polyprotein the virus-like particles consisted
of p24 protein and a negligible amount of non-processed Gag precursor
s. The share of p24 protein increased in proportion to the duration of
coinfection and decreased with a reduction of multiplicity of infecti
on with rVV carrying p160Gag-Pol. Hence, the absence of p6 domain does
not influence the processing of Gag proteins during virus-like partic
les assembly and budding. In contrast to the natural systems of HIV-I
development, in the rVV expression system the p6Gag domain virtually d
oes not contribute to reactions between Gag and Gag-Pol precursors and
to the particles' morphogenesis.