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. Author manuscript; available in PMC: 2013 Jul 1.
Published in final edited form as: Mol Microbiol. 2012 May 24;85(1):21–38. doi: 10.1111/j.1365-2958.2012.08081.x

Figure 5.

Figure 5

Ribosome diffusion in untreated cells. (A) Trajectories of single ribosomes (S2-YFP labels) within one cell, plotted within a spherocylinder chosen to match the phase contrast image. (B) Mean-square displacement vs lag time, averaged over 53 single-molecule trajectories from the same cell, each consisting of 13 steps. Error estimates are ±1σof the MSD values from single molecules. Dashed line is a linear fit to first three data points, yielding a diffusion coefficient estimate of D = 0.035 μm2-s−1. Colored swath represents the range of theoretical MSDr(τ) plots (± one standard deviation of the mean) obtained from averaging fifty 13-step Monte Carlo simulated trajectories using D = 0.04 μm2-s−1, the best-fit value as judged by eye. The simulations were run in a spherocylinder within which two truncated cylinders (representing the segregated DNA nucleoid lobes) block ribosome diffusion, as shown in the inset.

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