Against the backdrop of the limitations of both PCR tests and rapid diagnostic tests, a research group led by Young Min Song, PhD, of the Gwangju Institute of Science and Technology in Korea has recently developed a new slow light technique to easily visualize viruses using an optical microscope. A recent study explains in detail the operating principle of their detection platform, called the “Gires–Tournois immunoassay platform” (GTIP). This paper was made available online on March 22, 2022, and was published in the journal Advanced Materials on March 26, 2022.
The key element of GTIP is the Gires–Tournois “resonance structure,” a film made from three stacked layers of specific materials that produce a peculiar optical phenomenon called slow light. Because of how incident light rebounds inside the resonant layers before being reflected, the color of the platform seen through an optical microscope appears very uniform. However, nanometer-sized virus particles affect the resonance frequency of GTIP in their immediate vicinity by slowing down the light that gets reflected around them. The “slow light” manifests as a vivid color change in the reflected light so that, when viewed through the microscope, the virus particle clusters look like “islands” of a different color compared to the background.
To ensure that their slow light system only detects coronavirus particles, the researchers coated the top layer of GTIP with antibody proteins specific to SARS-CoV-2. Interestingly, not only did the system enable the detection of viral particles, but, by using colorimetric analysis techniques, the researchers could even effectively quantify the number of virus particles present in different areas of a sample depending on the color of the light reflected locally.
The overall simplicity of the design is one of the main selling points of GTIP. As Song explains, “Compared to existing COVID-19 diagnostic methods, our approach enables rapid detection and quantification of SARS-CoV-2 without needing extra sample treatments, such as amplification and labeling.” Given that optical microscopes are available in most laboratories, the method developed by the group could become a valuable and ubiquitous diagnostic and virus research tool.
Furthermore, GTIP is not limited to detecting viruses or strictly dependent on antibodies; any other binding agent works as well, helping visualize all kinds of particles that interact with light. “Our strategy can even be applied for a dynamic monitoring of target particles sprayed in the air or dispersed on surfaces. We believe that this approach could be the basis for next-generation biosensing platforms, enabling simple yet accurate detection,” concludes Prof. Song.
Featured Image: The novel slow light detection platform is fast, accurate, and performs label-free imaging of virus particles by slowing down light. Illustration: Gwangju Institute of Science and Technology (GIST)
