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. 2020 Jun 1;94(12):e00387-20. doi: 10.1128/JVI.00387-20

FIG 6.

FIG 6

MuV P and NP phosphorylation in cells with RPS6KB1 deficiency. (A) Representative radio blot. HeLa cells were transfected with siRNA, infected with MuV at an MOI of 0.1, and then labeled with 35S or 33P for 6 to 8 h. Cell lysates were immunoprecipitated with monoclonal anti-MuV P or anti-MuV NP antibody and resolved on an SDS-PAGE gel. (B) Total P protein quantification. Shown is 35S-labeled P protein from infected HeLa cells. Values were standardized to that of the nontarget control. (C) Relative phosphorylation levels of P in infected cells. The relative level was calculated as a ratio of phosphorylated protein (33P) to total protein (35S) and standardized to the nontarget control. P values were calculated using Student's t test. *, P < 0.5. The error bars represent SEM of data from 3 individual experiments.