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. 2015 Sep 16;89(23):11820–11833. doi: 10.1128/JVI.02274-15

FIG 4.

FIG 4

Effects of proteasomal and lysosomal inhibitors on ORF7a antagonism of BST-2. (A and B) HEK293T cells were treated with either ConA or MG-132 to demonstrate that the concentrations used are inhibitory to proteasomal or lysosomal degradation, respectively. The lysate was analyzed by Western blotting with antibodies against ubiquitin (α-Ub) (A) and LC3B (B) to demonstrate the efficacies of the compounds. (C) Increasing amounts of ORF7a were transfected into HEK293T cells. The cells were subsequently treated with the lysosome inhibitor concanamycin A or the proteasome inhibitor MG-132. Neither inhibitor prevented BST-2 antagonism by ORF7a. The data shown are representative of those from three independent experiments. The numbers next to the gels in panels A to C are molecular masses (in kilodaltons).