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Related Concept Videos

Super-resolution Fluorescence Microscopy01:37

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Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been...
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Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM
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Open-source sub-nanometer stabilization system for super-resolution fluorescence microscopy.

Florencia Edorna1,2, Florencia D Choque1,2, Giovanni Ferrari1,3

  • 1Centro de Investigaciones en Bionanociencias (CIBION), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Ciudad Autónoma de Buenos Aires, Argentina.

Light, Science & Applications
|November 19, 2025
PubMed
Summary
This summary is machine-generated.

We developed an active stabilization system for super-resolution microscopy, achieving sub-nanometer precision for hours. This system enhances techniques like MINFLUX and RASTMIN for visualizing single molecules.

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Area of Science:

  • Optical microscopy
  • Nanotechnology
  • Biophysics

Background:

  • Super-resolution fluorescence microscopy achieves 1-10 nm resolution for visualizing individual molecules.
  • High precision requires rigorous sample drift control, especially for techniques like MINFLUX and RASTMIN.
  • Active drift correction is essential for nanometer-scale resolution in microscopy.

Purpose of the Study:

  • To present an active stabilization system for super-resolution microscopy.
  • To achieve sub-nanometer precision stabilization for extended periods.
  • To provide an adaptable and open-source solution for enhanced microscopy performance.

Main Methods:

  • Development of a simple optical design for an active stabilization module.
  • Integration of open-source control software with a user-friendly graphical interface.
  • Demonstration with p-MINFLUX and RASTMIN measurements in diverse experimental setups.

Main Results:

  • The stabilization system delivers sub-nanometer precision for hours.
  • The system is adaptable as a module for various fluorescence microscopes.
  • Measurements reached the theoretical Cramér-Rao Bound, resolving ~10 nm distances in DNA origami.

Conclusions:

  • The active stabilization system significantly improves super-resolution microscopy precision.
  • The open-source nature and adaptability facilitate widespread adoption.
  • The system enables robust visualization of nanoscale structures in biological environments.