Literature DB >> 28644014

Three-Dimensional Localization of an Individual Fluorescent Molecule with Angstrom Precision.

Taku Furubayashi, Kazuya Motohashi, Keisuke Wakao, Tsuyoshi Matsuda, Isao Kii1, Takamitsu Hosoya2, Nobuhiro Hayashi, Mahito Sadaie3, Fuyuki Ishikawa3, Michio Matsushita, Satoru Fujiyoshi4.   

Abstract

Among imaging techniques, fluorescence microscopy is a unique method to noninvasively image individual molecules in whole cells. If the three-dimensional spatial precision is improved to the angstrom level, various molecular arrangements in the cell can be visualized on an individual basis. We have developed a cryogenic reflecting microscope with a numerical aperture of 0.99 and an imaging stability of 0.05 nm in standard deviation at a temperature of 1.8 K. The key optics to realize the cryogenic performances is the reflecting objective developed by our laboratory. With this cryogenic microscope, an individual fluorescent molecule (ATTO647N) at 1.8 K was localized with standard errors of 0.53 nm (x), 0.31 nm (y), and 0.90 nm (z) when 106 fluorescence photons from the molecule were accumulated in 5 min.

Year:  2017        PMID: 28644014     DOI: 10.1021/jacs.7b03899

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Deciphering a hexameric protein complex with Angstrom optical resolution.

Authors:  Hisham Mazal; Franz-Ferdinand Wieser; Vahid Sandoghdar
Journal:  Elife       Date:  2022-05-26       Impact factor: 8.713

2.  Solid immersion microscopy images cells under cryogenic conditions with 12 nm resolution.

Authors:  Lin Wang; Benji Bateman; Laura C Zanetti-Domingues; Amy N Moores; Sam Astbury; Christopher Spindloe; Michele C Darrow; Maria Romano; Sarah R Needham; Konstantinos Beis; Daniel J Rolfe; David T Clarke; Marisa L Martin-Fernandez
Journal:  Commun Biol       Date:  2019-02-21
  2 in total

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