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. 2022 Jul 4;121(15):2906–2920. doi: 10.1016/j.bpj.2022.06.036

Figure 5.

Figure 5

Experimental observations of nuclear pore complexes within primary mouse neurons, antibody-labeled with AlexaFluor647. (a) (Left) Reconstructed image (10 nm pixels, 10 nm Gaussian blur) with yellow dashed line indicating the region of interest interrogated. (Right) A magnified subset from the white square region of larger image (1 nm pixels, 4 nm Gaussian blur) along with a scatterplot of localizations with color representing the observation time. Scale bars, 2 μm (left) and 200 nm (right top and bottom). (b) Autocorrelations as a function of displacement g(r,τ), tabulated from localizations for time interval windows centered at the values shown. (c) Δg(r,τ)=g(r,τ)g(r,τmax=685s) for the examples shown in (b). (d) Δg(r,τ) are fit to Δg(r,τ)exp{r2/4σxy2} to extract the LSF width in each lateral dimension. Error bars represent estimates of the standard error obtained through bootstrapping. The average LSF width for this image is σxy= 10.9 ± 0.8 nm. To see this figure in color, go online.