Role of the sarcin-ricin loop of 23S rRNA in biogenesis of the 50S ribosomal subunit

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FIGURE 4.
FIGURE 4.

Nonribosomal proteins associated with affinity-purified 50S particles. (A) Shown are the predicted stoichiometries of each nonribosomal protein detected at a level of >0.01 for either control (blue) or mutant (orange) particles. Bars represent the mean ± SEM of three biological replicates. Inset shows the collective abundance of all nonribosomal proteins bound. Units represent ribosome stoichiometry, where 1.0 corresponds to the median r-protein value. Thus, isolated control subunits contain ∼1.5 nonribosomal proteins on average, while isolated ΔSRL particles contain ∼2.7. Based on a two-tailed paired t-test, P < 0.05. (B) For the same 41 nonribosomal proteins, fold enrichment (ΔSRL/control) values are shown. Data represent the quotient of two means ± standard error. For IlvC, ArgG, and NuoF, no protein was detected in any of the control sample replicates, so an enrichment value of 100 was assigned arbitrarily.

This Article

  1. RNA 31: 585-599