Johns Hopkins Medicine researchers report that food science principles have helped them determine how unusual droplets within cells stay organized and avoid dissolving into the rest of the cell's gelatinous interior.
The researchers say their work could advance scientific understanding of cell evolution and help scientists in the food and chemical industry develop better ways to keep liquid mixtures from separating.
The cells of all living organisms hold a collection of mini biological machines called organelles. These structures run the cell's powerhouse mitochondria, brainy nucleus and other operations, all with a defined border and encased in a membrane. However, there are other cell parts that appear as viscous, membrane-free "blobs," but they serve distinct purposes, such as regulating genes, sending chemical signals or storage sites for specialized molecules.
Scientists have long thought these somewhat mystifying droplets might be a primordial version of organelles, and the Johns Hopkins-led research team worked with laboratory worms to study them further.
A report on the research team's findings about these droplets, which are called biomolecular condensates, appears Sept. 10 in Science.
I hope this work will help convince scientists that biomolecular condensates are highly sophisticated cellular compartments. We found they have regulated roles and respond to the environment, just like other organelles. And we found that they do have membranes, just not the type we're used to seeing."
Geraldine Seydoux, Ph.D., the Huntington Sheldon Professor in Medical Discovery and vice dean for basic research at the Johns Hopkins University School of Medicine and investigator at the Howard Hughes Medical Institute
Biomolecular condensates were first dubbed "granules" in the 1970s by scientists who used electron microscopy to peer more closely at the structures in many organisms, including squiggly creatures called C. elegans, whose relatively simple biology has made them a common laboratory model for studying everything from modern gene-cutting technology to protein structure. The condensates in worms, which look tough and similar in appearance to grains of sand, are known as P granules.
In 2014 in Seydoux's lab, graduate student Jennifer Wang conducted genetic analyses to find a protein called MEG-3 in worm P granules. Wang's experiments showed that another protein, PGL-3, creates the viscous liquid droplets, the "core" of P granules, and that MEG-3 loiters on the outside of the P granule, making small "clusters" that coat the surface of the P granules.
"What we didn't understand was these proteins could just linger on the outside of P granules yet be so integral to stabilizing the interior of the granules," says Seydoux.
The mystery was still unsolved when, in January, 2020, Seydoux was looking for the right words to describe their observations. She Googled "solids stabilizing liquids" and found references to the food science concept of Pickering emulsions. "I had an OMG moment when I read more about this phenomenon," says Seydoux.
An emulsion is a mixture of two liquids that don't normally mix well, like oil and water. A Pickering emulsion is such a mixture that is stabilized, like the everyday carton of milk from the grocery store.
Unprocessed cow milk is naturally unstable, and the fat droplets in milk tend to glom together to reduce the overall surface area among the fat molecules. The fat molecules — or cream — rise to the top and separate from the whey, or watery liquid in the milk.
To avoid milk separation and stabilize the liquid, dairy processors push milk through a small needle, which breaks up the fat droplets, coats them with a protein called casein and avoids creating a creamy layer of fused fat molecules.
Seydoux says it occurred to her that MEG-3 might act in a way very similar to casein's effect in milk, lowering the surface tension of the droplets to keep them from fusing together. And MEG-3's tendency to remain around the surface of P granules suggested to her that it acted as a kind of membrane, she adds.
In their experiments, Seydoux and her team showed that PGL-3 droplets coated with MEG-3 stay evenly separated on glass slides, with twice as many droplets compared with uncoated condensates that fuse together, forming fewer and larger droplets on the glass slide.
"This is a well-known phenomenon in food science, and now we see that it may also be happening inside a cell," says Seydoux.
Seydoux and her team also engineered worm egg cells that lacked MEG-3 and saw that the uncoated P granules dissolved more slowly. This and other experiments, says Seydoux, suggest that MEG-3 not only stabilizes the droplets under normal conditions but also allows the droplets to respond more quickly when environmental conditions change.
Seydoux's team of postdoctoral students, including cell imaging specialist Andrew Folkmann and biochemist Andrea Putnam, sought help to complete their studies from an expert in physical chemistry who could guide them through the physics of Pickering emulsions.
Several months after adding bioengineer Chiu Fan Lee from the Imperial College of London to the team, he helped them identify a missing component in their MEG-3 worm model: an enzyme called MBK-2 that helps the liquid inside P granules become less viscous.
"Together, these experiments provide an explanation for how this primordial soup inside cells can assemble into compartments that resist fusing together and that respond to developmental cues," says Seydoux.
The team plans further studies to determine the precise physical structure of MEG-3 and additional details about how it works. If further studies pan out, MEG-3 could provide a renewable resource for developing Pickering emulsions in the food and chemical industry, they say.
Seydoux and the team have filed patents on the use of MEG-3 as a tool for developing Pickering emulsions.
Johns Hopkins Medicine
Folkmann, A.W., et al. (2021) Regulation of biomolecular condensates by interfacial protein clusters. Science. doi.org/10.1126/science.abg7071.
Posted in: Cell Biology | Life Sciences News
Tags: Cell, Cell Imaging, Electron, Electron Microscopy, Enzyme, Evolution, Food, Gene, Genes, Genetic, Imaging, Laboratory, Medicine, Membrane, Microscopy, Mitochondria, pH, Protein, Research, students
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