Spatial Statistics of Three-Dimensional Growth Dynamics of Spindle Microtubules
The latest high-resolution 3D live-cell imaging technology, lattice light-sheet microscopy (LLSM), has successfully tracked the dynamics of microtubule growth throughout the entire mitotic spindle with unparalleled precision. By using green fluorescent protein-labeled end-binding protein 1 (EB1-GFP) as a marker for growing microtubule ends, LLSM has generated an extensive collection of multidimensional datasets mapping the positions and trajectories of these growing microtubule ends. Processing this data requires statistical analysis in three-dimensional space. This chapter describes the spatial statistical methods developed for this purpose, illustrated with practical examples. Finally, we discuss future prospects for analyzing complex, large-scale image data.
Authors
- Norio Yamashita (ORCID: https://orcid.org/0000-0001-8044-9016)
- Hideo Yokota (ORCID: https://orcid.org/0000-0003-1395-309X)
- Yuko Mimori‐Kiyosue (ORCID: https://orcid.org/0000-0003-3513-9072)
- Masahiko Morita
Institutions
- Kansai Medical University (JP)
- RIKEN Center for Biosystems Dynamics Research (JP)
- RIKEN Center for Advanced Photonics (JP)
Publication Details
- Journal
- Methods in molecular biology
- Published
- 2024-12-01
- DOI
- https://doi.org/10.1007/978-1-0716-4224-5_4
- Citations
- 3
- Primary Topic
- Advanced Fluorescence Microscopy Techniques
- Type
- article
- Field-Weighted Citation Impact
- 7.23
Funders
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency
- RIKEN
- Core Research for Evolutional Science and Technology
- RIKEN Center for Biosystems Dynamics Research