Tokyo, Japan - April 26, 2024
Yokogawa Electric Corporation's latest single-cell analysis solution, the Single Cellome™ System SS2000, has been featured in an article published in the high-profile journal Analytical Chemistry regarding groundbreaking work conducted by researchers at the University of Surrey in the emerging field of single-cell lipidomics*1. The SS2000 is a live cell image device equipped with Yokogawa's original dual-microlens spinning disk imaging technology, and enables cutting-edge life science research.
Image 1. Single Cellome System SS2000
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Lipidomics is the large-scale study of lipids, a large family of molecules that play biological roles ranging from maintaining normal operation of the human body to the development of major diseases*2. Lipidomic studies are conventionally conducted by bulk isolation and analysis of lipids from many cells. While bulk lipid analyses can provide scientists a population average of the lipid profile, they are unable to discern subtle cell-to-cell variations or reveal the spatial or temporal differences to the lipidome caused by cell-cell interactions.
Single-cell lipidomics is an emerging field where the lipid composition of single cells is analyzed. These studies help overcome the challenges of bulk lipidomics by offering scientists a means of exploring spatial and temporal differences in addition to intercellular variability. Understanding these differences is key to creating a more complete picture to understand diseases such as cancer*2. One challenge facing researchers is the ability to isolate single cells in a way that maintains the natural lipidome of a cell. Current methods of single-cell isolation detach and suspend multiple cells at once and then isolate them through a narrow channel, but this can be particularly stressful to cells and may result in alterations to cellular lipid make up. Yokogawa's Single Cellome System SS2000 uses confocal imaging technology to help abrogate challenges with single-cell lipidomics. It is a dual-purpose system that enables live cell imaging and also performs fully automated single-cell and subcellular sampling without going through the suspension process, thereby minimizing stress on the cells.
SS2000 application example
Yokogawa's collaborators at the University of Surrey have shown that Yokogawa's SS2000 is a vast improvement over other single-cell isolation technologies in the context of single-cell lipidomics. With the ability to sample adherent cells in culture, the SS2000 has allowed researchers to maintain the natural lipid profile of sampled cells while also providing spatial and temporal information based on real time imaging. The researchers have taken advantage of this unique dual capability to create a workflow that is not feasible with other technologies. They have coupled the spatial and temporal information gained from the SS2000's dual-microlens spinning disk imager with liquid chromatography mass spectrometry data conducted on each sampled cell. This novel approach is a radical step forward in the field of lipidomics, which will help lead to breakthroughs in alternative treatments and therapies for cancer, diabetes, and cardiovascular disease*2.
In this way, Yokogawa will continue to provide our customers with new value and the latest technology, and help ensure well-being for all.
*2 Zehua Wang, Mingjun Cao, Sin Man Lam, Guanghou Shui. Embracing lipidomics at single-cell resolution: Promises and pitfalls. TrAC Trends in Analytical Chemistry, Volume 160, 2023, 116973, ISSN 0165-9936, https://doi.org/10.1016/j.trac.2023.116973.
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Yokogawa’s high content analysis systems and dual spinning disk confocal technologies provide high-speed and high-resolution live cell imaging, enabling leading-edge research around the world.
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Equipped with a minimally-invasive nanopipette, our Single Cellome Unit is capable of injecting target substances while maintaining the positional information of individual cells.
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Subcellular Sampling System SS2000
The SS2000 is a system that automatically samples specific regions of cells or whole cells at the single-cell level while imaging cells in culture with a confocal microscope. Because cells in culture do not need to be detached, positional and morphological information is maintained.