Super-resolution Microscopy in Plant Cell Imaging
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem, přehledy
PubMed
26482957
DOI
10.1016/j.tplants.2015.08.013
PII: S1360-1385(15)00228-9
Knihovny.cz E-zdroje
- Klíčová slova
- photoactivation localization microscopy, plant cell biology, stimulated emission depletion microscopy, stochastic optical reconstruction microscopy, structured-illumination microscopy, super-resolution microscopy,
- MeSH
- mikroskopie metody MeSH
- rostlinné buňky chemie fyziologie ultrastruktura MeSH
- zobrazování trojrozměrné MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- přehledy 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.
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