Virion incorporation of the Nef7.A3G fusion protein. 293T cells were
transfected with
HIV.env–.nef– and WT Nef,
Nef7, Nef7.A3G, or A3G expression plasmids with pcDNA3 included as a control.
Progeny viruses were collected and subjected to Western blot (WB)
analysis along with whole cell lysate using an antibody against an HA epitope
that was added to the C terminus of all Nefs, Nef7.A3G, and A3G and antibodies
against HIV-1 p24 or β-actin as loading controls (A) followed by
quantitation of the protein level in virions from three independent
experiments, as stated above (B).