Super-resolution Microscopy in Plant Cell Imaging
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
26482957
DOI
10.1016/j.tplants.2015.08.013
PII: S1360-1385(15)00228-9
Knihovny.cz E-resources
- Keywords
- photoactivation localization microscopy, plant cell biology, stimulated emission depletion microscopy, stochastic optical reconstruction microscopy, structured-illumination microscopy, super-resolution microscopy,
- MeSH
- Microscopy methods MeSH
- Plant Cells chemistry physiology ultrastructure MeSH
- Imaging, Three-Dimensional MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
Although the development of super-resolution microscopy methods dates back to 1994, relevant applications in plant cell imaging only started to emerge in 2010. Since then, the principal super-resolution methods, including structured-illumination microscopy (SIM), photoactivation localization microscopy (PALM), stochastic optical reconstruction microscopy (STORM), and stimulated emission depletion microscopy (STED), have been implemented in plant cell research. However, progress has been limited due to the challenging properties of plant material. Here we summarize the basic principles of existing super-resolution methods and provide examples of applications in plant science. The limitations imposed by the nature of plant material are reviewed and the potential for future applications in plant cell imaging is highlighted.
References provided by Crossref.org
Comparing Super-Resolution Microscopy Techniques to Analyze Chromosomes
Prospects and limitations of expansion microscopy in chromatin ultrastructure determination
Super-Resolution Microscopy Reveals Diversity of Plant Centromere Architecture