This article explores the use of expansion microscopy, a technique that enhances resolution in fluorescence microscopy, on the autotrophic protist Euglena gracilis A modified protocol was developed to preserve the cell structures during fixation. Using antibodies against key cytoskeletal and organelle markers, α-tubulin, β-ATPase, and Rubisco activase, the microtubular structures, mitochondria, and chloroplasts were visualised. The organisation of the cytoskeleton corresponded to the findings from electron microscopy while allowing for the visualisation of the flagellar pocket in its entirety and revealing previously unnoticed details. This study offered insights into the shape and development of mitochondria and chloroplasts under varying conditions, such as culture ages and light cycles. This work demonstrated that expansion microscopy is a robust tool for visualising cellular structures in E. gracilis, an organism whose internal structures cannot be stained using standard immunofluorescence because of its complex pellicle. This technique also serves as a complement to electron microscopy, facilitating tomographic reconstructions in a routine fashion.

• MeSH
• Chloroplasts ultrastructure   MeSH
• Cytoskeleton * ultrastructure   MeSH
• Euglena gracilis * ultrastructure   MeSH
• Flagella ultrastructure   MeSH
• Microscopy, Fluorescence * methods   MeSH
• Mitochondria ultrastructure   MeSH
• Mitosis MeSH
• Antibodies chemistry   MeSH
• Publication type
• Journal Article MeSH
• Names of Substances
• Antibodies MeSH