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. 2017 Sep 12;114(39):10338–10343. doi: 10.1073/pnas.1702226114

Fig. 4.

Fig. 4.

Simultaneous measurements of shape fluctuations of CGS and NE upon biochemical perturbations. (A) Micrographs of cell nuclei expressing both H2B-mCherry (green) and LMNA-GFP (red) under the following conditions: control, after ATP depletion, and upon addition of α-amanitin, blebbistatin, latrunculin A, and nocodazole. (B) Fluctuations u2 of CGS (green) and NE (red) for each condition from A at one time point. Average and instantaneous contours for CGS and NE are shown in Fig. S6. (C) Wavenumber-dependent uq2 under the following conditions: control (n = 27), ATP depletion (n = 24), α-amanitin (n = 15), blebbistatin (n = 15), latrunculin A (n = 16), and nocodazole (n = 18) treatment. Black curves represent negative control by fixation with formaldehyde for CGS (markers) and NE (no markers). Solid black lines illustrate slopes q2 and q4. Error bars are shown in Fig. S6. (D) PSD of uq2 as a function of wavelength λ upon different perturbations. (Scale bar, 5 μm.)