| Literature DB >> 20923631 |
Tomonobu M Watanabe, Shingo Fukui, Takashi Jin, Fumihiko Fujii, Toshio Yanagida.
Abstract
Superresolution optical microscopy (nanoscopy) is of current interest in many biological fields. Superresolution optical fluctuation imaging, which utilizes higher-order cumulant of fluorescence temporal fluctuations, is an excellent method for nanoscopy, as it requires neither complicated optics nor illuminations. However, it does need an impractical number of images for real-time observation. Here, we achieved real-time nanoscopy by modifying superresolution optical fluctuation imaging and enhancing the fluctuation of quantum dots. Our developed quantum dots have higher blinking than commercially available ones. The fluctuation of the blinking improved the resolution when using a variance calculation for each pixel instead of a cumulant calculation. This enabled us to obtain microscopic images with 90-nm and 80-ms spatial-temporal resolution by using a conventional fluorescence microscope without any optics or devices.Mesh:
Year: 2010 PMID: 20923631 PMCID: PMC3042578 DOI: 10.1016/j.bpj.2010.07.036
Source DB: PubMed Journal: Biophys J ISSN: 0006-3495 Impact factor: 4.033