Document Type
Article
Language
eng
Format of Original
17 p.
Publication Date
1-2016
Publisher
American Society for Cell Biology
Source Publication
Molecular Biology of the Cell
Source ISSN
1059-1524
Original Item ID
doi: 10.1091/mbc.E15-08-0608
Abstract
The microtubule (MT) plus-end tracking protein EB1 is present at the tips of cilia and flagella; end-binding protein 1 (EB1) remains at the tip during flagellar shortening and in the absence of intraflagellar transport (IFT), the predominant protein transport system in flagella. To investigate how EB1 accumulates at the flagellar tip, we used in vivo imaging of fluorescent protein–tagged EB1 (EB1-FP) in Chlamydomonas reinhardtii. After photobleaching, the EB1 signal at the flagellar tip recovered within minutes, indicating an exchange with unbleached EB1 entering the flagella from the cell body. EB1 moved independent of IFT trains, and EB1-FP recovery did not require the IFT pathway. Single-particle imaging showed that EB1-FP is highly mobile along the flagellar shaft and displays a markedly reduced mobility near the flagellar tip. Individual EB1-FP particles dwelled for several seconds near the flagellar tip, suggesting the presence of stable EB1 binding sites. In simulations, the two distinct phases of EB1 mobility are sufficient to explain its accumulation at the tip. We propose that proteins uniformly distributed throughout the cytoplasm like EB1 accumulate locally by diffusion and capture; IFT, in contrast, might be required to transport proteins against cellular concentration gradients into or out of cilia.
Recommended Citation
Harris, J. Aaron; Liu, Yi; Yang, Pinfen; Kner, Peter; and Lechtreck, Karl F., "Single-particle imaging reveals intraflagellar transport–independent transport and accumulation of EB1 in Chlamydomonas flagella" (2016). Biological Sciences Faculty Research and Publications. 502.
https://epublications.marquette.edu/bio_fac/502
Comments
Published version. Molecular Biology of the Cell, Vol. 27, No. 2 (January 2016): 295-307. DOI. © 2016 American Society for Cell Biology. Used with permission.