Optics.org
daily coverage of the optics & photonics industry and the markets that it serves
Featured Showcases
Photonics West Showcase
Optics+Photonics Showcase
News
Menu
Research & Development

‘Ghost imaging’ speeds up super-resolution microscopy

17 Dec 2019

New nanoscopy approach to capture biological processes occurring inside cells at sub-ms speeds.

Researchers at the Chinese Academy of Sciences (CAS), Beijing, China, have used advanced imaging techniques to achieve what they describe as “super-resolution microscopy at unprecedented speeds.” The new method should make it possible to capture the details of processes occurring in living cells at speeds not previously possible.

Super-resolution techniques, often called nanoscopy, achieve nano-scale resolution by overcoming the diffraction limit of light. Although nanoscopy can capture images of individual molecules inside cells, it is difficult to use with living cells because hundreds or thousands of imaging frames are needed to reconstruct an image — a process too slow to capture quickly changing dynamics.

The research has been reported in Optica, in which the CAS investigators describe how they used an unconventional imaging approach known as “ghost imaging” to enhance the imaging speed of nanoscopy.

This combination produces nanometer resolution using orders of magnitude fewer imaging frames than required by traditional nanoscopy techniques.

“Our imaging method can potentially probe dynamics occurring on millisecond time-scales in subcellular structures with spatial resolution of tens of nanometers – the spatial and temporal resolution at which biological processes take place,” said Zhongyang Wang, co-leader of the research team.

Combining techniques

The new approach is based on stochastic optical reconstruction microscopy (STORM), which was one of three super-resolution techniques to be recognized with Nobel prizes in 2014. STORM, which is also sometimes called photoactivated localization microscopy (PALM), is a wide-field technique that uses fluorescent labels that switch between light-emitting (on) and dark (off) states.

Acquiring hundreds or thousands of snapshots, each capturing the subset of fluorescent labels that are on at a given time, allows the location of each molecule to be determined and used to reconstruct a fluorescence image.

The researchers turned to ghost imaging to speed up the STORM imaging process. Ghost imaging forms an image by correlating a light pattern that interacts with the object with a reference pattern that does not.

Individually, the light patterns do not carry any meaningful information about the object. The researchers also used compressive imaging, a computational approach that enables image reconstruction with fewer exposures because it uses an algorithm to fill in the missing information.

“While STORM requires a low density of fluorescent labels and many image frames, our approach can create a high-resolution image using very few frames and a high density of fluorophores,” said co-leader of research team Shensheng Han.

“It also doesn’t need any complex illumination, which helps reduce photobleaching and phototoxicity that could harm dynamic biological processes and living cells.”

Improving imaging efficiency

To implement the new technique, the researchers used an optical component known as a random phase modulator to turn fluorescence from the sample into a random speckle pattern. Coding the fluorescence in this way allowed each pixel of a very fast CMOS camera to collect light intensity from the whole object in a single frame.

To form the image via ghost imaging and compressive imaging, this light intensity was correlated with a reference light pattern in a single step. The result was more efficient image acquisition and a reduction in the number of frames required to form a high-resolution image.

The researchers tested the technique by using it to image a 60-nanometer ring. The new nanoscopy approach could resolve the ring using just 10 image frames while traditional STORM approaches needed up to 4000 frames to achieve the same result. The new approach also resolved a 40nm ruler with 100 image frames.

“We hope this method can be applied to a variety of fluorescent samples, including those that exhibit weaker fluorescence than those used in this research,” said Wang. The researchers also want to make the technique faster to achieve video-rate imaging with a large field of view and plan to use it to acquire 3D and color images.

Optikos Corporation LaCroix Precision OpticsSacher Lasertechnik GmbHChangchun Jiu Tian  Optoelectric Co.,Ltd.CHROMA TECHNOLOGY CORP.AlluxaHyperion Optics
© 2024 SPIE Europe
Top of Page