Author:
Hugelier Siewert,Vandenberg Wim,Lukeš Tomáš,Grußmayer Kristin S.,Eilers Paul H. C.,Dedecker Peter,Ruckebusch Cyril
Abstract
AbstractSub-diffraction or super-resolution fluorescence imaging allows the visualization of the cellular morphology and interactions at the nanoscale. Statistical analysis methods such as super-resolution optical fluctuation imaging (SOFI) obtain an improved spatial resolution by analyzing fluorophore blinking but can be perturbed by the presence of non-stationary processes such as photodestruction or fluctuations in the illumination. In this work, we propose to use Whittaker smoothing to remove these smooth signal trends and retain only the information associated to independent blinking of the emitters, thus enhancing the SOFI signals. We find that our method works well to correct photodestruction, especially when it occurs quickly. The resulting images show a much higher contrast, strongly suppressed background and a more detailed visualization of cellular structures. Our method is parameter-free and computationally efficient, and can be readily applied on both two-dimensional and three-dimensional data.
Funder
Fonds Wetenschappelijk Onderzoek
European Research Council
H2020 Marie Skłodowska-Curie Actions
Publisher
Springer Science and Business Media LLC
Cited by
4 articles.
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