Proceedings of the National Academy of Sciences · 2012 · 522 citations · 39 references
Natural SciencesBiophysicsCell BiologyBiomedical ImagingCell BiophysicsMolecular ImagingCellular ImagingCellular UltrastructureEndomembrane SystemFluorescence MicroscopyMitochondrial FissionSuper-resolution MicroscopyDynamic ImagingLive-cell Imaging ProbesMorphological DynamicsNanometer-scale ImagingSmall-molecule Imaging ProbesSuper-resolution Fluorescence ImagingSuper-resolution Fluorescence MicroscopySuper-resolution Imaging
Imaging cellular membranes at nanometer resolution can reveal organelle ultrastructure and dynamics essential for cell function. The study aimed to identify photoswitchable membrane probes and use them to acquire super‑resolution fluorescence images of live‑cell membranes. Eight small‑molecule probes targeting the plasma membrane, mitochondria, ER, and lysosomes were shown to photoswitch efficiently and label live cells at high density, enabling super‑resolution imaging. Using these probes, the authors obtained 30–60 nm spatial resolution and 1–2 s temporal resolution images, including two‑color super‑resolution of mitochondria and ER, revealing previously hidden details of mitochondrial fusion/fission, ER remodeling, and heterogeneous membrane diffusivity on neuronal processes.
Imaging membranes in live cells with nanometer-scale resolution promises to reveal ultrastructural dynamics of organelles that are essential for cellular functions. In this work, we identified photoswitchable membrane probes and obtained super-resolution fluorescence images of cellular membranes. We demonstrated the photoswitching capabilities of eight commonly used membrane probes, each specific to the plasma membrane, mitochondria, the endoplasmic recticulum (ER) or lysosomes. These small-molecule probes readily label live cells with high probe densities. Using these probes, we achieved dynamic imaging of specific membrane structures in living cells with 30–60 nm spatial resolution at temporal resolutions down to 1–2 s. Moreover, by using spectrally distinguishable probes, we obtained two-color super-resolution images of mitochondria and the ER. We observed previously obscured details of morphological dynamics of mitochondrial fusion/fission and ER remodeling, as well as heterogeneous membrane diffusivity on neuronal processes.
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