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. 2000 Oct;74(20):9580–9585. doi: 10.1128/jvi.74.20.9580-9585.2000

FIG. 2.

FIG. 2

SDS-polyacrylamide gel electrophoresis separation of 35S-labeled proteins synthesized in VSV-infected MEFs from PKR−/− and control animals. MEFs were either not infected (−) or infected with VSV at an MOI of 3 for 2, 4, 6, or 8 h as described in Materials and Methods. The infected cells at each time point were pulsed with [35S]methionine-cysteine for 1 h prior to being harvested and lysed. VSV proteins (G, N, and M) begin to appear in PKR−/− and control cells at 4 h p.i. While this pattern of labeled proteins remains constant in control cells up to 8 h p.i. viral proteins become the predominant translated proteins in the PKR−/− samples by 8 h p.i. Molecular masses are indicated at left of each panel in kilodaltons.