Paper
5 November 2018 Two-photon excitation structured illumination super-resolution microscopy
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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.
© (2018) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Wei Zheng "Two-photon excitation structured illumination super-resolution microscopy", Proc. SPIE 10816, Advanced Optical Imaging Technologies, 1081608 (5 November 2018); https://doi.org/10.1117/12.2502292
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KEYWORDS
Adaptive optics

Microscopy

Super resolution

Wavefronts

Imaging systems

Super resolution microscopy

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