Subdiffraction-Resolution Fluorescence Microscopy of Myosin-Actin Motility

Subdiffraction‐resolution imaging by subsequent localization of single photoswitchable molecules can achieve a spatial resolution in the range of ∼20 nm with moderate excitation intensities, but have so far been too slow for imaging faster dynamics in biology. Herein, we introduce a novel approach for video‐like subdiffraction microscopy based on rapid and reversible photoswitching of commercially available organic carbocyanine fluorophores. With the present concept, we demonstrate in vitro studies on the motility of fluorophore‐labeled actin filaments along myosin II. Actin filaments were densely labeled with carbocyanine fluorophores, and the gliding velocity adjusted by the concentration of ATP. At imaging frame rates of ∼100 Hz, only 100 consecutive frames are sufficient to generate a single high‐resolution image of moving actin filaments with a lateral resolution of ∼30 nm. A video‐like sequence is generated from individual reconstructed images by additionally applying a sliding window algorithm. We measured velocities of individual actin filaments of up to ∼0.18 μm s−1, observed strong bending and disruption of filaments as well as locally immobile fragments. Moving pictures: Video‐like dSTORM with a spatial resolution of ∼30 nm is achieved by exploiting fast photoswitching of organic fluorophores. In vitro studies on the motility of fluorophore‐labeled actin filaments along myosin II is presented (see picture) and velocities of up to ∼0.18 μm s−1for the actin filaments are observed.