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. 2018 Aug 16;115(6):1055–1067. doi: 10.1016/j.bpj.2018.08.010

Figure 5.

Figure 5

Mobility of both actin and microtubules in composites exhibits a nonmonotonic dependence on tubulin fraction. (AC) 2 × 2 images show binary skeletonization of a single frame (top row) and temporal color maps (bottom row) of movies for (A) ϕT = 0, (B) ϕT = 1, and (C) ϕT = 0.5 networks. Full 512 × 512 images (left) as well as zoomed-in images (right, corresponding to box in left-hand images) are shown. The different colors in temporal color maps correspond to different times during each 180 s movie. Colors go from red at 0 to magenta at 180 s, as shown in the scale bar to the right of each map. (D) The standard deviation of intensity values, σI, over all pixels and all frames of each time series, normalized by the corresponding mean, <I>, versus tubulin fraction ϕT, is shown. σI/<I> is calculated separately for actin and microtubule channels to determine the mobility of each filament in composites. Error bars are the standard error from averaging over 512 × 512 pixels in 3–5 images for each ϕT. As shown, the mobility of both actin (circles) and microtubules (squares) increases as ϕT increases to 0.5, followed by a subsequent drop. Color coding represents the different ϕT values, as in Figs 2, 3, and 4. To see this figure in color, go online.