Enhanced Raman microscopy of cryofixed specimens: clearer and sharper chemical imaging
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Enhanced Raman microscopy of cryofixed specimens: clearer and sharper chemical imaging

30/12/2024 Osaka University

Researchers from Osaka University use cryogenic freezing to achieve high-resolution Raman microscopy images of biological samples

Osaka, Japan – Understanding the behavior of the molecules and cells that make up our bodies is critical for the advancement of medicine. This has led to a continual push for clear images of what is happing beyond what the eye can see. In a study recently published in Science Advances, researchers from Osaka University have reported a method that gives high-resolution Raman microscopy images.

Raman microscopy is a useful technique for imaging biological samples because it can provide chemical information about specific molecules—such as proteins—that take part in the body’s processes. However, the Raman light that comes from biological samples is very weak, so the signal can often get swamped by the background noise, leading to poor images.

The researchers have developed a microscope that can maintain the temperature of previously frozen samples during the acquisition. This has allowed them to produce images that are up to eight times brighter than those previously achieved with Raman microscopy.

“One of the main reasons for blurry images is the motion of the things you’re trying to look at,” explains lead author of the study, Kenta Mizushima. “By imaging frozen samples that were unable to move, we could use longer exposure times without damaging the samples. This led to high signals compared with the background, high resolution, and larger fields of view.” The technique uses no stains and doesn’t require any chemicals to fix the cells in position, so can provide a highly representative view of processes and cell behavior.

The team was also able to confirm that the freezing process conserved the physicochemical states of different proteins. This gives the cryofixing approach a distinct advantage of achieving what the chemical fixing methods cannot.

“Raman microscopy adds a complementary option to the imaging toolbox,” says senior author Katsumasa Fujita. “The fact that it not only provides cell images, but also information about the distribution and particular chemical states of molecules, is very useful when we are continually striving to achieve the most detailed possible understanding.”

The new technique can be combined with other microscopy techniques for detailed analysis of biological samples and is expected to contribute to a wide range of areas in the biological sciences including medicine and pharmaceutics.

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The article, “Raman microscopy of cryofixed biological specimens for high-resolution and high-sensitivity chemical imaging,” was published in Science Advances at DOI: https://www.science.org/doi/10.1126/sciadv.adn0110
Title: Raman microscopy of cryofixed biological specimensfor high-resolution and high- sensitivitychemical imaging
Journal: Science Advances
Authors: Kenta Mizushima, Yasuaki Kumamoto, Shoko Tamura, Masahito Yamanaka, Kentaro Mochizuki, Menglu Li, Syusuke Egoshi, Kosuke Dodo, Yoshinori Harada, Nicholas I. Smith, Mikiko Sodeoka, Hideo Tanaka, Katsumasa Fujita
DOI: 10.1126/sciadv.adn0110
Funded by: Japan Science and Technology Agency
Attached files
  • Fig. 1 Raman image of rapidly frozen HeLa cells with high signal-to-noise ratio and large field-of-view. The image acquisition time was 10 hours. The distribution of Raman signals from cytochromes (750 cm⁻¹), lipids (2850 cm⁻¹), proteins (2920 cm⁻¹), are indicated in green, red, and blue, respectively., CC BY, Sci. Adv. 10, eadn0110 (2024)
  • Fig. 2 Schematic of the sample area in the developed cryo-Raman microscope. A cover glass with cultured cells is placed on the sample mount, and a metal plate is brought into contact (left). The cryogen enters through the inlet and a hole in the metal plate, coming into direct contact with the sample for rapid freezing. The sample temperature is controlled by the metal plate with liquid nitrogen circulation and a heater inside (right)., CC BY, Sci. Adv. 10, eadn0110 (2024)
  • Fig. 3 Raman images of rapidly frozen HeLa cells captured with different exposure times (left) and the relationship between the Raman signal intensity, attributed to different molecular vibrations, and exposure time (right). The observation temperature was -40°C., CC BY, Sci. Adv. 10, eadn0110 (2024)
30/12/2024 Osaka University
Regions: Asia, Japan
Keywords: Applied science, Engineering

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