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Figure 4 | Virology Journal

Figure 4

From: Involvement of PKR and RNase L in translational control and induction of apoptosis after Hepatitis C polyprotein expression from a Vaccinia virus recombinant

Figure 4

Time-course analysis of cellular and viral protein synthesis in cells expressing HCV polyprotein. A: BSC40 cells infected with the recombinant VT7-HCV7.9 virus in the presence (+) or absence (-) of IPTG were metabolically labelled with [35S] Met-Cys Promix (50 μCi/mL) at the indicated times (h.p.i) and analysed by SDS-PAGE (12%) and autoradiography. For comparative purposes, we included a similar inducible recombinant virus but expressing the IBDV mature structural capsid protein VP3 (VT7-VP3). B: Inhibition of VV proteins after expression of HCV. The levels of VV proteins were quantitated from autoradiograms using a BioRad GS700 image densitometer and computer software as suggested by the manufacturer. C: Immunoblot analysis of phospho-eIF-2α-S51 protein levels during the time-course of VT7-HCV7.9 infection. The number appearing in each lane represents the ratio of phospho-eIF-2α-S51 levels in infected cells compared to levels in uninfected cells.

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