Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Dec 1;29(25):3017–3025. doi: 10.1091/mbc.E18-01-0022

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 2018 Hayashi et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.

This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.

PMC Copyright notice

FIGURE 5: — Measurement of χ for retrogradely transported endosomes in axon. (A) The traces of χ plotted against Δt for anterograde endosomes (n = 119). They were classified into three clusters by k-means clustering (indicated with different colors; see Materials and Methods for the details). The distribution of χ* is shown as a histogram. The positions of the cluster centers are indicated by arrows. (B) The fluctuation χ^* is plotted against the square root of fluorescence intensity (FI), which is a proxy for the radius of the endosome. The color of each data point is the same as in the left panels in A, which reflects the number of FPUs. The average and the SD for each cluster are shown with square symbols with error bars. There was a weak correlation between χ^* and (FI)^1/2 (r = 0.33), as observed with anterograde endosomes (Figure 4B). (C) The χ^*–velocity relation. The colors for the data points are the same as in the other panels.