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Fast volumetric multifocus structured illumination microscopy of subcellular dynamics in living cells.

Maximilian Lukas SenftlebenAntone BajorEduardo Hirata-MiyasakiSara AbrahamssonHjalmar Brismar
Published in: Biomedical optics express (2024)
Studying the nanoscale dynamics of subcellular structures is possible with 2D structured illumination microscopy (SIM). The method allows for acquisition with improved resolution over typical widefield. For 3D samples, the acquisition speed is inherently limited by the need to acquire sequential two-dimensional planes to create a volume. Here, we present a development of multifocus SIM designed to provide high volumetric frame rate by using fast synchronized electro-optical components. We demonstrate the high volumetric imaging capacity of the microscope by recording the dynamics of microtubule and endoplasmatic reticulum in living cells at up to 2.3 super resolution volumes per second for a total volume of 30 × 30 × 1.8 µm 3 .
Keyphrases
  • living cells
  • single molecule
  • high resolution
  • fluorescent probe
  • atomic force microscopy
  • high speed
  • high throughput
  • mass spectrometry
  • optical coherence tomography
  • photodynamic therapy
  • label free
  • single cell