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Published on: July 30, 2014
Quantitative analysis of actin patch movement in yeast
A E Carlsson1, A D Shah, D Elking
1Department of Physics, Washington University, St. Louis, Missouri 63130, USA. aec@wuphys.wustl.edu
Biophysical Journal
|April 20, 2002
Summary
Computer tracking reveals yeast cortical actin patches move randomly. Actin depolymerization with latrunculin significantly reduces movement, though some directed motion persists in treated cells.
Area of Science:
- Cell Biology
- Biophysics
- Microscopy
Background:
- Cortical actin patches are crucial for yeast cell polarity and morphogenesis.
- Understanding their movement dynamics is key to elucidating cellular processes.
Purpose of the Study:
- To develop and apply a computational method for tracking yeast cortical actin patch motion.
- To investigate the impact of actin depolymerization on patch dynamics.
Main Methods:
- Utilized fluorescence microscopy to capture live yeast cell movies.
- Developed an image-processing algorithm to detect and track 2D patch coordinates.
- Applied a minimum-distance algorithm to connect patch trajectories across frames.
- Analyzed motion using mean-square displacements and a novel criterion for directed motion.
Main Results:
- Yeast cortical actin patch movement, on average, follows a random walk pattern.
- Treatment with latrunculin (an actin-depolymerizing agent) significantly reduced the diffusion coefficient of the patches.
- Latrunculin-treated cells exhibited lower mean-squared patch travel distances compared to control cells.
- Patches were found to move independently, with a notable degree of directed motion observed in control cells, and a lesser extent in treated cells.
Conclusions:
- The developed tracking method effectively quantifies actin patch dynamics.
- Actin polymerization is essential for directed cortical actin patch movement in yeast.
- While primarily random, directed motion plays a significant role in control cell dynamics.

