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Proceedings Paper

Two-photon excitation structured illumination super-resolution microscopy
Author(s): Wei Zheng
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Paper Abstract

Three dimensional (3D) fluorescence microscopy has proven essential in biological studies. It allows interrogation of structure and function at spatial scales spanning the macromolecular, cellular, and tissue levels. Two-photon excitation fluorescence microscopy (TPM) is especially well suited to 3D imaging in samples tens to hundreds of microns in thickness, enabling better background rejection than alternatives due to the long wavelength, nonlinear excitation of fluorescence. However, the spatial resolution of conventional TPM is limited by diffraction to ~0.3 um laterally and ~0.8 um axially. In this report, we will introduce our new developed two-photon excitation structured illumination microscopy which combines the two-photon microscopy capability and the super-resolution microscopy capability in the same system. In addition, optical aberrations caused by optical system and biological samples are determined using direct wavefront sensing with a nonlinear guide star (two-photon-excited fluorescence emitted either from the labeled sample or an exogenous marker) and subsequently corrected using a deformable mirror, restoring super-resolution information that is otherwise lost. We demonstrate that both resolution and fluorescence intensity of our super-resolution microscope is improved on a variety of samples, including bead phantoms, cultured cells in collagen gels, and Drosophila brain tissue slides.

Paper Details

Date Published: 5 November 2018
PDF: 7 pages
Proc. SPIE 10816, Advanced Optical Imaging Technologies, 1081608 (5 November 2018); doi: 10.1117/12.2502292
Show Author Affiliations
Wei Zheng, Shenzhen Institutes of Advanced Technology (China)


Published in SPIE Proceedings Vol. 10816:
Advanced Optical Imaging Technologies
Xiao-Cong Yuan; Kebin Shi; Michael G. Somekh, Editor(s)

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