TLN2

New results reveal a new mode of force transmission in which dynamic molecular stretching bridges the extracellular matrix and flowing F-actin moving at different speeds. This discovery underscores the necessity of molecular elasticity and random coupling for sufficiently transmitting force. The findings also call for revising the role of molecular unfolding. Cell biology has possibly never jumped to the next level in the same way. In multicellular organisms, cell migration and mechanosensing are essential for cellular development and maintenance. These processes rely on talin, the key focal adhesion -- or FA -- protein, central in connecting adjacent cellular matrices and enabling force transmission between them. Talins are commonly considered fully extended at FAs between actin filaments -- or F-actin -- and the anchor-like integrin receptor. Yet, a research team led by Kyoto University have previously observed that the actin network constantly moves over FAs as a single unit: a unique phenomenon contradicting prevailing notions. "This begs the question: how does talin manage to simultaneously maintain the intercellular connection while transmitting force?" asks corresponding author Sawako Yamashiro at KyotoU's Graduate School of Life Sciences. Most significantly, the team's results reveal a new mode of force transmission in which dynamic molecular stretching bridges the extracellular matrix and flowing F-actin moving at different speeds. This discovery underscores the necessity of molecular elasticity and random coupling for sufficiently transmitting force. "On a human scale, this phenomenon can be visualized as a super flexible anime character. He is gripping onto a train passing at around 50 km/h," illustrates Yamashiro. The train represents the flowing F-actin, while a station platform is the substrate. The superhero plays the talin FA protein that would either be carried away unstretched or remain on the substrate. "Occasionally, however, when both ends of talin are firmly anchored, it gets stretched by the pull because some parts of this protein can unfold like a spring," explains Yamashiro. Aided by intracellular fluorescent talin single-molecule imaging, Yamashiro's team observed and calculated that approximately 4% of the talin links the F-actin and the substrate via an elastic transient clutch. In contrast, the remaining majority are bound to either end. These findings also call for revising the role of molecular unfolding, updating the traditional view that it functions as a mechanosensor and a shock absorber when molecules unfold under external force. "However, our results suggest that molecular unfolding facilitates the transmission of force rather than absorbing it," says coauthor Dimitrios Vavylonis at Lehigh University. "We can expect further use of intracellular single-molecule microscopy to witness other possible intra- and extra-cellular superheroic behaviours, such as talin's elastic transient clutch," concludes coauthor Naoki Watanabe, also at KyotoU's Graduate School of Life Sciences.

Cells communicate with themselves and their cellular environment through mechanical bonds. This work advances understanding of the role of these forces on proteins as they interact to accomplish their biological functions, including the control of cancer. Talin is a protein that controls cellular attachment and movement, but its malfunctioning also allows cancer cells to spread. DCL1 is a tumor-suppressing protein. But scientists don't fully understand how either protein works -- or what happens when they don't work the way they should. One thing scientists doknow: When it is present in a cell, DCL1 can interact with talin and perhaps interfere with talin's ability to group cells together. If scientists knew the exact steps in the process, they may be able to identify a treatment option to keep cancer from metastasizing. To find answers, a team of researchers from the University of Wisconsin-Milwaukee used a unique tool that they built to apply the exact mechanical forces that act on talin in the body, beginning a process called protein unfolding that is necessary for the protein to perform its function. With the tool, called "single molecule magnetic tweezers," the scientists measured intracellular mechanical forces and experimented with them in the lab so that they can find what happens to talin when DCL1 is both present and not present in the cell. They have discovered a unique behavior of talin, induced by mechanical forces, that demonstrates a strong interaction that can explain the antitumor effect of DLC1 when the two proteins bind. "We still don't know exactly what goes wrong with talin functioning when cancer cells metastasize," said Ionel Popa, a UWM physics professor who led the team. "But it looks like talin plays a role in activating the spread of cells when the tumor-suppressing DCL1 is missing. And when DCL1 binds to talin, it appears to block talin from activating cell-spreading." The work is published today in the journal Science Advances. Like all proteins, talin forms a specific three-dimensional shape that defines its function. Known as protein folding, it is one of the most complex processes in nature and, when folding goes awry, it often leads to disease. Popa's lab investigates forces affecting protein folding, which can lead to new treatments for diseases that start when proteins misfold. For some proteins, including talin, mechanical forces inside and outside the cell are necessary for the protein to obtain the shape that unlocks its function. Inside the cells, mechanical forces prompt talin to unfold, revealing receptors where other proteins can bind to form needed messaging connections. "The process is like a mechanical computer because it calculates how much force is needed for all the connections to happen," Popa said. "These forces tell the cell what's going on around it." The cell produces various ligands, which convert mechanical forces to chemical signals when they bind to a protein. And the mechanical fine-tuning by these ligands, including DCL1, are what made the researchers so interested in talin to begin with. The location, or domain, where DCL1 binds with talin has the highest number of ligands available among all binding stations on the protein. In fact, messaging goes on both inside and outside the cell as ligands help orchestrate the task. Correlating and measuring the force mechanism of the folding has allowed the researchers to study this process in further detail. How the tweezers can 'see' Scientists already knew that DCL1 binds at only one particular domain on the talin protein. The UWM researchers revealed how: In response to an applied force, talin unfolds and refolds, forming a structure where DCL1 binds almost irreversibly. "We gathered the data from the talin molecule as it unfolded and refolded, and then added DCL1 to see how it changed," Popa said. "Previous research indicated a weak interaction, suggesting it's probably not the driver of DCL1's suppressor abilities. But when we tested it, we found the opposite -- the resulting molecule becomes super-stable." The magnetic tweezers allowed the researchers to make measurements on a protein molecule only a few nanometers in size. After tethering it between a glass surface and a paramagnetic bead, the researchers measure the position of the paramagnetic bead at a freely moving end of the molecule, and that of a nonmagnetic bead, glued to the same surface as the opposite end of the protein. Then they apply a magnetic force, replicating the exact mechanical perturbations exerted on a protein in the body, and measure its unfolding and refolding to understand how its structure changes. With the magnetic tweezers the researchers can investigate the effect of those forces over days rather than minutes, similar to their timelines in the body. The role of hormones The activation of talin during cell-spreading and tissue-building is controlled by hormones. In this stage, the protein undergoes cycles of stretching and binding with other proteins. Mechanical forces come into play as more proteins join the process. For talin to be activated, it must be brought to the cell membrane by messengers that signal from the cell cytoskeleton to the extracellular matrix, the surrounding environment that cells are embedded in. Popa's team tracked the effect of DCL1 in this process. "During this hormone-driven 'inside-out' activation, if DLC1 also binds to talin, it will not allow for that recruitment to the membrane," he said. "Any of the steps controlling cell spreading might be highjacked by cancer cells to become metastatic. In some cases, DLC1 is completely suppressed." Missing or malfunctioning DCL1 may not be the only factor in cancer spread, Popa said. But the work illustrates the alternate behaviors of proteins under force and points to a direction for further study for this protein interaction as a potential target for cancer drugs.