Three-dimensional sub–100 nm resolution fluorescence microscopy of thick samples

By M. Juette, T. Gould, M. Lessard, Michael J. Mlodzianoski, B. S. Nagpure, B. Bennett, Samuel T. Hess, J. Bewersdorf. Nature Methods, 2008

814 citations recorded by the source corpus.

Subfields: Biomedical Engineering, Biophysics

View Paper: https://www.semanticscholar.org/paper/e76392b155d60d210665d39662afc337214b5c95

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Citations in the corpus

Far-Field Optical Nanoscopy (2007, background): “All diffraction-unlimited nanoscopy methods can provide improved axial resolution even when implemented with a single lens [77, 83, 120, 131, 132].”
Fluorescent probes for super-resolution imaging in living cells (2008, methodology): “Using multifocal plane imaging, Juette and co-workers achieved 3D FPALM imaging with 30 nm resolution in the xy plane and 75 nm resolution in the axial dimensio”
Whole cell 3D STORM reveals interactions between cellular structures with nanometer-scale resolution (2008, neutral): “Similar axial resolutions have been subsequently obtained using bifocal plane imagin”
A guide to super-resolution fluorescence microscopy (2010, methodology): “…over an extended imaging depth of a few microns by either introducing an astigmatism, as in 3D STORM (Huang et al., 2008a,b), by a double-plane detection in biplane (BP) FPALM (Juette et al., 2008), or by engineering a double helix–shaped point spread function (DH-PSF; Pavani et al., 2009).”
Fluorophore localization algorithms for super-resolution microscopy (2014, background): “Biplane imaging 38 is even simpler from an image-processing standpoint, requiring just the fitting of two circular PSFs with variable width.”
Super resolution fluorescence microscopy (2009, background): “Another implementation of 3D superresolution imaging (54) uses two-focal-plane imaging, in which the emission light is split and imaged to two regions of the camera with different path lengths, allowing the determination of z coordinates from the defocused shape of the singlemolecule images.”
Three-dimensional sub-100 nm super-resolution imaging of biological samples using a phase ramp in the objective pupil (2011, methodology): “The existing approaches broadly fall in two classes: (1) acquisition of multiple simultaneous observations of the same molecule, as in the biplane [ 5 ] and iPALM [6] approaches, or (2) engineering of the 3D microscope poi nt spread function (PSF) so that 3D position information is encoded in the (d”