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International research team presents new imaging technique to make lipids in cellular membranes visible and show how they are organized at the nanoscale.
To the point:
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3D visualization of lipids with a new technique (Lipid-CLEM): Combining two imaging techniques, the researchers developed a correlative light and electron microscopy (CLEM) workflow to visualize and quantify individual lipids in cellular membranes at ultrastructural resolution.
Lipid organization and distribution in nanoscale clusters: Specialized regions in various cellular membranes, called nanodomains, are important for key cellular functions like signaling and transport. The new imaging workflow revealed that the lipid, sphingomyelin is distributed differently in various parts of the membrane of early endosomes, showing that lipids must be sorted in this organelle. So far, this sorting has been demonstrated only for proteins at this detail.
New possibility to study complex membrane systems: The Lipid-CLEM technique provides the first reliable way to map the distribution of lipids in 3D within complex cellular structures. This will allow researchers to build a comprehensive model of biological membranes in the future that includes both lipids and proteins.
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Biological membranes of cells and its subunits (organelles) are organized into tiny regions (nanodomains) made up of fats (lipids) and proteins. Those specialized regions carry out important tasks for the cell, such as signaling, sorting, or transport. While proteins in these domains are well understood, the lipid distribution and behavior within them remain a bit of a mystery, as lipids move very quickly and existing methods struggle to visualize individual lipid species at high resolution.
To localize lipids, researchers use "bifunctional lipid probes," which are very small, slightly modified lipids that act like molecular GPS tags. These probes can be added into living cells, then “frozen in place” with light (photo-crosslinking), and later labeled with fluorescence using a chemical reaction (click chemistry). In this way, researchers can track where specific lipids are and not alter and disturb the cell too much.
However, light microscopy alone is not enough to visualize small details in the cell membrane. Higher details can be captured by electron microscopy. Correlative light and electron microscopy (CLEM) combines the strengths of both techniques. Together with the bifunctional lipid probes, Lipid-CLEM shows where labeled lipids are and makes the fine structure of the membranes visible.
Previous CLEM methods, though, either damaged the membrane structure, only worked on the outer surface of the cell, or couldn’t distinguish individual lipid species. To fix these issues, Mathilda Lennartz and a team of researchers in the group of André Nadler, group leader at the Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG) in Dresden, Germany, and the group of Ori Avinoam at the Weizmann Institute of Science in Rehovot, Israel, have now developed a new method that they call Lipid-CLEM.
Novel 3D imaging of lipids
Mathilda Lennartz, co-corresponding and lead author of the study, explains, “To study lipid sorting in early endosomes – a key sorting station inside the cell – cells must be rapidly frozen to stop lipids in their tracks and to preserve the membrane of the cells. Later, these lipids can be labeled on very thin slices of the sample, termed "sections," of cells using click chemistry. These sections are what we then image using the Lipid-CLEM approach.”
“With Lipid-CLEM, we observed that a specific lipid called sphingomyelin is more common in small vesicles inside the endosome and less common in tubular membrane domains. This separation has already been observed for some proteins,” says Mathilda. “What we concluded from this is that at least some lipids, just like proteins, must also be sorted in the endosome. Interestingly, in our study, sphingomyelin and a protein cargo arrive at the same time in the early endosome but separate into different domains, indicating that lipid and protein trafficking routes can diverge during this sorting.”
The power of team work
Ori Avinoam’s team at the Weizmann Institute brought in their expertise in correlative light and electron microscopy to this study. Ori says, “This study highlights how essential collaborations are for driving research forward. Bringing together complementary expertise allowed us to establish a method that made it possible to uncover fundamental principles of lipid sorting that were previously inaccessible.”
André Nadler, corresponding author, summarizes, “Our Lipid-CLEM workflow enables 3D visualization of lipid densities in membrane nanodomains, offering a new way to study lipid organization in complex cellular structures. We finally can look at lipid sorting in membranes with the resolution we need. We believe that our new method Lipid-CLEM will help us to better understand how lipids work in cells, as it allows us to study both lipids and proteins together during membrane organization and function. This may also contribute to a better understanding of membrane dysfunction-related diseases.”
Dr. André Nadler
nadler@mpi-cbg.de
H. Mathilda Lennartz, Suman Khan, Weihua Leng, Kristin Böhlig, Gunar Fabig, Yannick Kieswald, Falk Elsner, Nadav Scher, Michaela Wilsch-Bräuninger, Ori Avinoam, André Nadler: Visualizing sub-organellar lipid distribution using correlative light and electron microscopy. Nat Cell Biol (2026), doi: 10.1038/s41556-026-01915-x
https://www.mpi-cbg.de/news-outreach/news-media/article/busy-lipids-in-nano-hots...
Lipid localisation at early endosomes: The 3D membrane outlines of an early endosome are overlayed w ...
Quelle: H. Mathilda Lennartz / MPI-CBG
Copyright: H. Mathilda Lennartz / MPI-CBG
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