Abstract

This paper reports our original technique for visualizing cell-attached nanointerfaces with extremely high axial resolution using homogeneously excited localized surface plasmon resonance (LSPR) on self-assembled silver nanoparticle sheets. The LSPR sheet can confine and enhance the fluorescence at the nanointerface, which provides high signal-to-noise ratio images of focal adhesion at the cell-attached interface. The advantage of this LSPR-assisted technique is its usability, which provides comparable or higher-quality nanointerfacial images than TIRF microscopy, even under epifluorescence microscopy. We also report the cytotoxicity of silver nanoparticles, as determined via morphological analysis of adherent cells on the sheet.

Highlights

  • The demand for super-resolution fluorescence microscopy is increasing within the field of cell biology because of the requirement to investigate molecular-level dynamic reactions in or near cells[1,2,3]

  • The optical microscopic images of the RBL-2H3 cells attached to oleylamine-capped gold nanoparticles (AuOA) after overnight incubation is shown for comparison in the supporting data

  • We reported that the optical field intensity excited by localized surface plasmon resonance (LSPR) on the AgMy sheet was confined to less than a 10 nm region from the centre of the particles, based on the finite-difference time-domain (FDTD) calculation[8]

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Summary

Introduction

The demand for super-resolution fluorescence microscopy is increasing within the field of cell biology because of the requirement to investigate molecular-level dynamic reactions in or near cells[1,2,3]. Is confocal laser scanning microscopy (CLSM) utilized as a standard tool for high-resolution fluorescence imaging, simulated emission depletion (STED) microscopy, structured illumination microscopy (SIM), photoactivated localization microscopy (PALM), and stochastic optical reconstruction microscopy (STORM) are utilized as a family of super-resolution microscopy techniques. These super-resolution microscopy techniques have an advantage in their lateral resolution but are not as advantageous in either their axial resolution or temporal resolution because of their scanning criteria[4].

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