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Home > Research Teams > Biophysics and Biophotonic > Super-resolution microscopy and time-resolved imaging > Microscopies au delà de la limite de diffraction > Microscopie DONALD > DONALD microscopy

DONALD microscopy

by Leveque-Fort Sandrine - 17 August 2015 (modifié le 20 August 2015)

Direct Optical Nanoscopy with Axially Localized Detection - DONALD

One of the main challenge in SMLM is to improve the axial positioning accuracy which is typically between 20 and 50 nm, and which gives only a relative positioning of the fluorophores. By coupling the microscope SMLM with a detection module providing access to the supercritical angle fluorescence emission (SAF), the axial position of the fluorophore can be retrieved and gives the absolute distance regarding the glass slide supporting the cell. The DONALD microscopy (Direct Optical Nanoscopy with Axially Localized Detection) achieves an isotropic resolution below 20 nm.
This technique has just been the object of a publication in Nature Photonics http://www.nature.com/nphoton/journ.... A video summary is also available (https://youtu.be/Wf8iHYww9lY) or (https://vimeo.com/135072198).

A super-resolved 3D image example is shown below. Actin of the cell is labeled with the Alexa 647, on the left representing the image diffraction limited subnetwork is not discernable in contrast to the super-resolved image (right part of the image )

This work is developped in collaboration with Institut Langevin-ESPCI PArisTech (team E. Fort) et le Centre de photonique biomédicale de Paris Sud (G. Dupuis, S.Lécart). We were funded by thel ANR and the DIM NanoK.