scispace - formally typeset
Open AccessJournal ArticleDOI

Nanoscopy on-a-chip: super-resolution imaging on the millimeter scale

Reads0
Chats0
TLDR
The advent of large field-of-view chip-based nanoscopy opens up new routes in diagnostics where high throughput is needed for the detection of non-diffuse disease, or rare events such as the early detection of cancer.
Abstract
Optical nanoscopy techniques can image intracellular structures with high specificity at sub-diffraction limited resolution, bridging the resolution gap between optical microscopy and electron microscopy. So far conventional nanoscopy lacks the ability to generate high throughput data, as the imaged region is small. Photonic chip-based nanoscopy has demonstrated the potential for imaging large areas, but at a lateral resolution of 130 nm. However, all the existing super-resolution methods provide a resolution of 100 nm or better. In this work, chip-based nanoscopy is demonstrated with a resolution of 75 nm over an extraordinarily large area of 0.5 mm × 0.5 mm, using a low magnification and high N.A. objective lens. Furthermore, the performance of chip-based nanoscopy is benchmarked by studying the localization precision and illumination homogeneity for different waveguide widths. The advent of large field-of-view chip-based nanoscopy opens up new routes in diagnostics where high throughput is needed for the detection of non-diffuse disease, or rare events such as the early detection of cancer.

read more

Citations
More filters
Journal ArticleDOI

Structured illumination microscopy using a photonic chip

TL;DR: In this paper, a planar photonic chip is used to hold a biological sample and generate the necessary light patterns for structured illumination microscopy, which enables live-cell super-resolution imaging of subcellular structures at high speeds.
Journal ArticleDOI

Structured illumination microscopy using a photonic chip

TL;DR: In this article, a photonic-chip-based total internal reflection fluorescence (TIRF)-SIM was proposed to reduce the complexity of the optical setup needed to acquire TIRF-SIM images.
Journal ArticleDOI

On-chip TIRF nanoscopy by applying Haar wavelet kernel analysis on intensity fluctuations induced by chip illumination.

TL;DR: This work proposes to perform Haar wavelet kernel (HAWK) analysis on the original image stack prior to the application of SOFI, and demonstrates resolution enhancement as well as reduction in artifacts through the combination of HAWK and SOFI.
Journal ArticleDOI

Challenges facing quantitative large-scale optical super-resolution, and some simple solutions

TL;DR: The unique set of challenges facing quantitative SRM are discussed, giving particular attention to the shortcomings of conventional specimen preparation techniques and the necessity for optimal labeling of molecular targets.
Journal ArticleDOI

Chip-Based Resonance Raman Spectroscopy Using Tantalum Pentoxide Waveguides

TL;DR: In this paper, the authors demonstrate resonance Raman measurements of hemoglobin, a crucial component of blood, at 532-nm excitation using a tantalum pentoxide (Ta2O5) waveguide platform.
References
More filters
Journal ArticleDOI

Imaging intracellular fluorescent proteins at nanometer resolution.

TL;DR: This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
Journal ArticleDOI

Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

TL;DR: A high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores that can, in principle, reach molecular-scale resolution is developed.
Journal ArticleDOI

Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

TL;DR: A new type of scanning fluorescence microscope capable of resolving 35 nm in the far field is proposed, overcome the diffraction resolution limit by employing stimulated emission to inhibit the fluorescence process in the outer regions of the excitation point-spread function.
Journal Article

Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy

TL;DR: In this paper, the authors proposed a new type of scanning fluorescence microscope capable of resolving 35 nm in the far field by employing stimulated emission to inhibit the fluorescence process in the outer regions of the excitation point spread function.
Journal ArticleDOI

Ultra-High Resolution Imaging by Fluorescence Photoactivation Localization Microscopy

TL;DR: A new method for fluorescence imaging has been developed that can obtain spatial distributions of large numbers of fluorescent molecules on length scales shorter than the classical diffraction limit, and suggests a means to address a significant number of biological questions that had previously been limited by microscope resolution.
Related Papers (5)