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Innovative sample preparation using alcohol dehydration and high refractive index medium enables acquisition of two-channel super-resolution 3D STED image of an entire oocyte
M. Frolikova, M. Blazikova, M. Capek, H. Chmelova, J. Valecka, V. Kolackova, E. Valaskova, M. Gregor, K. Komrskova, O. Horvath, I. Novotny
Language English Country England, Great Britain
Document type Journal Article
Grant support
CZ.02.1.01/0.0/0.0/16_019/0000827
European Regional Development Fund
68378050-KAV-NPUI
European Regional Development Fund
CZ.1.05/1.1.00/02.0109
European Regional Development Fund
LM2023050
MEYS
CZ.02.1.01/0.0/0.0/18_046/0016045
MEYS
GA-22-30494S
Grant Agency of the Czech Republic
GA-21-21736S
Grant Agency of the Czech Republic
LX22NPO5102
European Union - Next Generation EU
CZ.02.1.01/0.0/0.0/16
European Regional Development Fund
CZ.02.1.01/0.0/0.0/16
ERDF
CZ.02.1.01/0.0/0.0/16_019/0000827
ERDF
PubMed
39392013
DOI
10.1111/jmi.13363
Knihovny.cz E-resources
- MeSH
- Alcohols MeSH
- Microscopy, Fluorescence methods MeSH
- Mice MeSH
- Specimen Handling methods MeSH
- Oocytes * MeSH
- Refractometry methods MeSH
- Imaging, Three-Dimensional * methods MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Super-resolution (SR) microscopy is a cutting-edge method that can provide detailed structural information with high resolution. However, the thickness of the specimen has been a major limitation for SR methods, and large biological structures have posed a challenge. To overcome this, the key step is to optimise sample preparation to ensure optical homogeneity and clarity, which can enhance the capabilities of SR methods for the acquisition of thicker structures. Oocytes are the largest cells in the mammalian body and are crucial objects in reproductive biology. They are especially useful for studying membrane proteins. However, oocytes are extremely fragile and sensitive to mechanical manipulation and osmotic shocks, making sample preparation a critical and challenging step. We present an innovative, simple and sensitive approach to oocyte sample preparation for 3D STED acquisition. This involves alcohol dehydration and mounting into a high refractive index medium. This extended preparation procedure allowed us to successfully obtain a unique two-channel 3D STED SR image of an entire mouse oocyte. By optimising sample preparation, it is possible to overcome current limitations of SR methods and obtain high-resolution images of large biological structures, such as oocytes, in order to study fundamental biological processes. Lay Abstract: Super-resolution (SR) microscopy is a cutting-edge tool that allows scientists to view incredibly fine details in biological samples. However, it struggles with larger, thicker specimens, as they need to be optically clear and uniform for the best imaging results. In this study, we refined the sample preparation process to make it more suitable for SR microscopy. Our method includes carefully dehydrating biological samples with alcohol and then transferring them into a mounting medium that enhances optical clarity. This improved protocol enables high-resolution imaging of thick biological structures, which was previously challenging. By optimizing this preparation method, we hope to expand the use of SR microscopy for studying large biological samples, helping scientists better understand complex biological structures.
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