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Biology subjects

Belsley, M.

Publications and source records attributed to Belsley, M..

2 recordsLinked to original sources

Bridging the resolution-sectioning gap in stimulated emission depletion microscopy: theory and experiment

Microscopes generally exhibit superior performance in 2D compared to 3D. Fluorescence super-resolution imaging often intensifies this discrepancy, such as with the gold-standard vortex-based stimulated emission depletion (STED) microscope, which narrows the point-spread function only laterally. In this study, we developed a semi-analytical theory based on the Nijboer-Zernike expansion, conducted simulations and performed experiments to establish the merits of the alternative bivortex-based STED. We find that this mode reduces the axial-lateral resolution mismatch and effectively emulates noisier multi-beam approaches by providing access to point-spread function geometries that are strictly forbidden to the two conventional single-beam modes, 2D-STED and z-STED. Notably, theory and experiment indicate that, besides filling the gap, bivortex STED delivers a higher signal-to-background than the two modes it bridges.

biophysics↗

Coherent-hybrid STED: a tunable photo-physical pinhole for super-resolution imaging at high contrast

Resolution in microscopy is not limited by diffraction as long as a nonlinear sample response is exploited. In a paradigmatic example, stimulated-emission depletion (STED) fluorescence microscopy fundamentally breaks the diffraction limit by using a structured optical pattern to saturate depletion on a previously excited sample area. Two-dimensional (2D) STED, the canonical low-noise STED mode, structures the STED beam by using a vortex phase mask, achieving a significant lateral resolution improvement over confocal fluorescence microscopy. However, axial resolution and optical sectioning remain bound to diffraction. Here we use a tunable coherent-hybrid (CH) beam to improve optical sectioning, markedly reducing background fluorescence. CH-STED, which inherits the 2D-STED immunity to spherical aberration, diversifies the depletion strategy, allowing an optimal balance between two key metrics (lateral resolution and background suppression) to be found. CH-STED is used to perform high-contrast imaging of complex biological structures, such as the mitotic spindle and the neuron cell body.

biophysics↗