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Faculty Introduction

Jae-Byum Chang (Google Scholar)

Department of Materials Science and Engineering

Bioimaging
Laboratory : https://sites.google.com/site/jbchang03/
Teacher start-up company : Flashomics Corp. (https://www.flashomics.com/)
Research LIST

Research contents

Professor Jae-Byum Chang's research team has been exploring advanced techniques for imaging a larger number of biomolecules within a single tissue. This cutting-edge field, known as multiplexed imaging, has recently gained significant attention in cancer and brain research. Studies have revealed that the types of cells within cancer patients' tissues exhibit considerable variation. Research findings suggest that the cellular composition and spatial distribution within a tumor are critical in determining the cancer type and its responsiveness to anticancer therapies. Professor Chang's team is actively developing innovative technologies to visualize and analyze the cellular and molecular diversity within tissues.

Research results

Source: Seo, J., Sim, Y., Kim, J., Kim, H., Cho, I., Nam, H., Yoon, Y.-G., & Chang, J.-B. (2022). PICASSO allows ultra-multiplexed fluorescence imaging of spatially overlapping proteins without reference spectra measurements. Nature Communications, 13(2475). https://www.nature.com/articles/s41467-022-30168-z. Licensed under CC BY 4.0, https://creativecommons.org/licenses/by/4.0/.

Professor Jae-Byum Chang's research team has been developing a technology that enables imaging multiple proteins within tissues through a simple experimental process, without the need for specialized equipment. One notable result of their work is the PICASSO technology, which was introduced by Professor Chang’s lab in 2022 (Nat. Commun., 13, 2475 (2022)). This technology allows the simultaneous use of fluorescent molecules with overlapping emission spectra to label and image multiple proteins. The resulting images are then processed using software to isolate the individual images of each protein.
Previously, technologies that used fluorescent molecules with overlapping emission spectra required precise measurement of the emission spectra for each molecule, posing significant limitations. However, PICASSO operates without such measurements, relying solely on the correlations among proteins present in the images. This eliminates the need for complex equipment, specialized chemical treatments, or spectral measurements, enabling the use of overlapping fluorescent molecules with ease.

Using this technology, Professor Chang’s team successfully imaged 15 proteins simultaneously in mouse brain tissue by employing 15 fluorescent molecules at once. They repeated this process three times, allowing them to image a total of 45 proteins in a single tissue sample through just three rounds of staining and imaging. Traditionally, only 3 to 4 fluorescent molecules could be used simultaneously, requiring over 10 rounds of staining and imaging to achieve comparable results. PICASSO significantly reduces this to three rounds, saving both time and cost.

Professor Chang’s research team plans to leverage this technology to study the molecular diversity within cancer and brain tissues. Their goals include identifying new cancer subtypes, selecting optimal anticancer drugs for specific subtypes, and discovering biomarkers for developing new drugs targeting these novel subtypes.