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- Guillaume Jacquemet
- Turku 1 , FI-20520 Turku , Finland
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- Alexandre F. Carisey
- William T. Shearer Center for Human Immunobiology, Baylor College of Medicine and Texas Children's Hospital 3 , 1102 Bates Street, Houston 77030 TX , USA
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- Hellyeh Hamidi
- Turku 1 , FI-20520 Turku , Finland
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- Ricardo Henriques
- University College London 4 , London WC1E 6BT , UK
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- Christophe Leterrier
- Aix Marseille Université, CNRS, INP UMR7051, NeuroCyto 6 , Marseille 13015 , France
書誌事項
- 公開日
- 2020-06-01
- 権利情報
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- http://www.biologists.com/user-licence-1-1
- DOI
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- 10.1242/jcs.240713
- 公開者
- The Company of Biologists
この論文をさがす
説明
<jats:title>ABSTRACT</jats:title> <jats:p>Fluorescence microscopy has become a ubiquitous method to observe the location of specific molecular components within cells. However, the resolution of light microscopy is limited by the laws of diffraction to a few hundred nanometers, blurring most cellular details. Over the last two decades, several techniques – grouped under the ‘super-resolution microscopy’ moniker – have been designed to bypass this limitation, revealing the cellular organization down to the nanoscale. The number and variety of these techniques have steadily increased, to the point that it has become difficult for cell biologists and seasoned microscopists alike to identify the specific technique best suited to their needs. Available techniques include image processing strategies that generate super-resolved images, optical imaging schemes that overcome the diffraction limit and sample manipulations that expand the size of the biological sample. In this Cell Science at a Glance article and the accompanying poster, we provide key pointers to help users navigate through the various super-resolution methods by briefly summarizing the principles behind each technique, highlighting both critical strengths and weaknesses, as well as providing example images.</jats:p>
収録刊行物
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- Journal of Cell Science
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Journal of Cell Science 133 (11), jcs240713-, 2020-06-01
The Company of Biologists

