Abstract

Recent years have seen a tremendous progress in the development of dielectric metasurfaces for visible light applications. Such metasurfaces are ultra-thin optical devices that can manipulate optical wavefronts in an arbitrary manner. Here, we present a newly developed metasurface which allows for coupling light into a microscopy coverslip to achieve total internal reflection (TIR) excitation. TIR fluorescence microscopy (TIRFM) is an important bioimaging technique used specifically to image cellular membranes or surface-localized molecules with high contrast and low background. Its most commonly used modality is objective-type TIRFM where one couples a focused excitation laser beam at the edge of the back focal aperture of an oil-immersion objective with high numerical aperture (N.A.) to realize a high incident-angle plane wave excitation above the critical TIR angle in sample space. However, this requires bulky and expensive objectives with a limited field-of-view (FOV). The metasurface which we describe here represents a low cost and easy-to-use alternative for TIRFM. It consists of periodic 2D arrays of asymmetric structures fabricated in TiO2 on borosilicate glass. It couples up to 70% of the incident non-reflected light into the first diffraction order at an angle of 65° in glass, which is above the critical TIR angle for a glass-water interface. Only ∼7% of the light leaks into propagating modes traversing the glass surface, thus minimizing any spurious background fluorescence originating far outside the glass substrate. We describe in detail design and fabrication of the metasurface, and validate is applicability for TIRFM by imaging immunostained human mesenchymal stem cells over a FOV of 200 µm x 200 µm. We envision that these kinds of metasurfaces can become a valuable tool for low-cost and TIRFM, offering high contrast, low photodamage, and high surface selectivity in fluorescence excitation and detection.

Highlights

  • During the last three decades, total internal reflection fluorescence (TIRF) microscopy has been the preferred choice among the very few commercially available high axial resolution optical microscopy techniques, due to its relative simplicity and virtually unrivaled performance for the study of cell membrane dynamics

  • TIRF systems, largely based on high numerical aperture (NA) oil objectives, rely on an evanescent field merely touching the observed sample to selectively excite those regions of interest, with no light reaching the bulk of the sample and significantly improving image contrast while minimizing photobleaching and photodamage

  • In order to exploit the unusually large field of view offered by MS-TIRF, the biological sample consisted on bone marrow Human Mesenchymal Stem Cells immunostained with anti-Paxillin and anti-rabbit IgG Atto 647N and mounted

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Summary

Introduction

During the last three decades, total internal reflection fluorescence (TIRF) microscopy has been the preferred choice among the very few commercially available high axial resolution optical microscopy techniques, due to its relative simplicity and virtually unrivaled performance for the study of cell membrane dynamics. A purposely designed MS grating redirects most of the free space incoming laser energy into one of the first diffraction orders, acting as a blazed grating light coupler for inexpensive, large FOV TIRF microscopy We experimentally demonstrate these MSs can couple up to 70% of the transmitted light into the first diffraction order at a 65° angle inside the glass substrate, sufficing total internal reflection conditions for a glass-water interface. The minimal direct transmission of 4% is a key characteristic of any MS design aimed for TIRF microscopy, due to the eventual close proximity between the MS and the stained biological sample and the fact that this beam will never be coupled into the glass substrate, potentially deteriorating the image’s contrast if stray light were to reach the observed sample

Fluorescence microscopy experimental setup and results
Findings
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