Cargando…

Combining 3D single molecule localization strategies for reproducible bioimaging

Here, we present a 3D localization-based super-resolution technique providing a slowly varying localization precision over a 1 μm range with precisions down to 15 nm. The axial localization is performed through a combination of point spread function (PSF) shaping and supercritical angle fluorescence...

Descripción completa

Detalles Bibliográficos
Autores principales: Cabriel, Clément, Bourg, Nicolas, Jouchet, Pierre, Dupuis, Guillaume, Leterrier, Christophe, Baron, Aurélie, Badet-Denisot, Marie-Ange, Vauzeilles, Boris, Fort, Emmanuel, Lévêque-Fort, Sandrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6491430/
https://www.ncbi.nlm.nih.gov/pubmed/31040275
http://dx.doi.org/10.1038/s41467-019-09901-8
Descripción
Sumario:Here, we present a 3D localization-based super-resolution technique providing a slowly varying localization precision over a 1 μm range with precisions down to 15 nm. The axial localization is performed through a combination of point spread function (PSF) shaping and supercritical angle fluorescence (SAF), which yields absolute axial information. Using a dual-view scheme, the axial detection is decoupled from the lateral detection and optimized independently to provide a weakly anisotropic 3D resolution over the imaging range. This method can be readily implemented on most homemade PSF shaping setups and provides drift-free, tilt-insensitive and achromatic results. Its insensitivity to these unavoidable experimental biases is especially adapted for multicolor 3D super-resolution microscopy, as we demonstrate by imaging cell cytoskeleton, living bacteria membranes and axon periodic submembrane scaffolds. We further illustrate the interest of the technique for biological multicolor imaging over a several-μm range by direct merging of multiple acquisitions at different depths.