2020
DOI: 10.1088/2050-6120/ab7e0f
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Spatial filter and its application in three-dimensional single molecule localization microscopy

Abstract: Single molecule localization microscopy (SMLM) allows the imaging of cellular structures with resolutions five to ten times below the diffraction limit of optical microscopy. It was originally introduced as a two-dimensional technique based on the localization of single emitters as projection onto the x-y imaging plane. The determination of the axial position of a fluorescent emitter is only possible by additional information. Here we report a method (spatial filter SMLM (SFSMLM)) that allows to determine the … Show more

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Cited by 8 publications
(2 citation statements)
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“…Super-resolution microscopy in epifluorescence mode was performed using an IX81 inverted microscope (Olympus, Tokyo, Japan) equipped with the MetaMorph Microscopy Automation and Image Analysis Software (Molecular Devices, San Jose, CA, United States) with a super-resolution module using a 60× oil immersion objective (NA = 1.49). For dSTORM imaging, the exposure time was set as 50 ms, and the electron-multiplying gain as 100× (Leduc et al, 2018;Fan et al, 2020). Alexa Fluor 647 (Jackson ImmunoResearch Laboratories, West Grove, PA, United States) or CF 568 (Biotium, Fremont, CA, United States) fluorescence was bleached using the full laser power until individual fluorophores began to blink (Supplementary Figure 2 and Supplementary Movie 1).…”
Section: Direct Stochastic Optical Reconstruction Microscopy Super-resolution Microscopymentioning
confidence: 99%
“…Super-resolution microscopy in epifluorescence mode was performed using an IX81 inverted microscope (Olympus, Tokyo, Japan) equipped with the MetaMorph Microscopy Automation and Image Analysis Software (Molecular Devices, San Jose, CA, United States) with a super-resolution module using a 60× oil immersion objective (NA = 1.49). For dSTORM imaging, the exposure time was set as 50 ms, and the electron-multiplying gain as 100× (Leduc et al, 2018;Fan et al, 2020). Alexa Fluor 647 (Jackson ImmunoResearch Laboratories, West Grove, PA, United States) or CF 568 (Biotium, Fremont, CA, United States) fluorescence was bleached using the full laser power until individual fluorophores began to blink (Supplementary Figure 2 and Supplementary Movie 1).…”
Section: Direct Stochastic Optical Reconstruction Microscopy Super-resolution Microscopymentioning
confidence: 99%
“…Superresolution microscopy was performed in TIRF mode using a home-built setup with an Olympus IX-71 inverted microscope body, an iXonEM+ DU897E (Andor) camera, and 405-, 488-/514-, 561-, and 642-nm lasers. An achromatic lens, used to focus the expanded laser beams on the back aperture of the objective (oil immersion objective, 60×, ApoN TIRF, numerical aperture 1.49; Olympus), was mounted on a movable stage to change focus position on the objective back aperture to switch between wide-field and TIRF mode ( 29 31 ). dSTORM ( 30 , 32 ) was performed in imaging buffer (90 mM β-mercaptoethylamine, 5% [wt/vol] glucose, 5% [vol/vol] glycerol, in phosphate-buffered saline; pH 7.4) and 20 μL oxygen-scavenging solution [0.1% (wt/vol) glucose oxidase, 0.12% (vol/vol) catalase, 50% (vol/vol) glycerol, 4 mM Tris(2-carboxyethyl)phosphine, 52 mM KCl, 20 mM Tris-HCl; pH 7.5].…”
Section: Methodsmentioning
confidence: 99%