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Biochemistry Research

Unlocking Cell Movement: Researchers Crack the Code on How Cells Travel Through the Body

Scientists have discovered how chemokines and G protein-coupled receptors selectively bind each other to control how cells move.

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Researchers from St. Jude Children’s Research Hospital and the Medical College of Wisconsin have made a groundbreaking discovery that sheds light on how cells travel through the body. By developing a data science framework, they were able to analyze chemokines and their associated G protein-coupled receptors (GPCRs), which are proteins that govern cell movement.

The scientists found that specific positions within structured and disordered regions of both proteins determine how chemokines and GPCRs bind each other. This understanding enabled them to artificially change chemokine-GPCR binding preferences and alter the resulting cell migration. Their findings have significant implications for disease treatment, such as enhancing cellular therapies’ ability to reach tumor sites, and increasing clarity about healthy processes like heart and blood vessel development.

Cell migration is a crucial process that influences many aspects of our bodies, including how immune cells travel to infection sites, brain development, and wound repair. However, the vast similarities between members of each protein family have presented a challenge in understanding how correct pairs form and control cell movement. The researchers’ data-driven approach identified the exact parts of each protein governing their molecular interactions.

“We found that cells have an elegant system that uses structure and disorder together to control cell migration,” said senior co-corresponding author M. Madan Babu, PhD. “With this understanding, we can now rationally introduce small changes in a chemokine’s structure to ultimately alter cell migration in desired ways.”

The scientists compared all human chemokine-binding GPCRs and all chemokines, then compared similar chemokines and GPCRs from other species. They also looked at each protein individually at a population level, finding places that stayed the same across groups and those that differed.

“Through our data analysis, we discovered that the information for how chemokines and GPCRs select for each other is stored in small, discrete packages of highly unstructured, disordered regions,” said first and co-corresponding author Andrew Kleist, MD. “The mix of those small packages from both the chemokine and receptor results in the unique interaction, similar to website data encryption keys, which governs cell migration.”

This discovery has significant implications for disease treatment and therapy development. The researchers’ framework can guide exploration into new medicines and improvements for existing cellular therapies.

“Now that we’ve shown a proof of concept, our approach will guide exploration into new medicines and improvements for existing cellular therapies,” Kleist said. “For example, it may be possible to create molecules that better lead immune cells to cancers or help recruit more blood stem cells for bone marrow transplants.”

The framework is freely available online at: https://github.com/andrewbkleist/chemokine_gpcr_encoding.

When people think about the body, we often think every cell stays in place. However, that’s a simplistic view. Depending on the tissue, cells are moving all the time, and our new understanding of those systems opens novel avenues for therapeutic development.

This discovery has the potential to revolutionize our understanding of cell movement and its role in various biological processes. By unlocking the code of cell movement, researchers can develop more effective treatments and therapies that target specific aspects of cellular behavior.

Biochemistry Research

The Double Edge of Love and War: How Female Earwigs Evolved Deadly Claws for Mate Competition

Female earwigs may be evolving exaggerated weaponry just like males. A study from Toho University found that female forceps, once assumed to be passive tools, show the same kind of outsized growth linked to sexual selection as the male’s iconic pincers. This means that female earwigs might be fighting for mates too specifically for access to non-aggressive males challenging long-standing assumptions in evolutionary biology.

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In a groundbreaking study published in the Biological Journal of the Linnean Society on June 12, 2025, researchers from Toho University have shed new light on the evolution of deadly claws in female earwigs. For decades, it was believed that these pincer-like appendages were exclusive to males and evolved solely as weapons in battles with rivals. However, the findings of Tomoki Matsuzawa (then an undergraduate) and Associate Professor Junji Konuma have challenged this notion, revealing a surprising parallel between male and female earwigs.

The researchers conducted a quantitative study on the maritime earwig Anisolabis maritima, analyzing the morphometric data of both sexes. They found that not only do females possess forceps, but they also exhibit positive allometry – a phenomenon where certain body parts grow disproportionately large relative to body size. This is strikingly similar to the pattern observed in males, suggesting that female earwigs may have evolved these traits through sexual selection.

In their study, the team measured various dimensions of the head, thorax, abdomen, and bilateral forceps, as well as shape differences between sexes. They discovered that males possess thick, short, and curved forceps, while females have thin, long, and straight ones – a clear example of sexual dimorphism. When they plotted body size against forceps width and length on a log-log scale, the results revealed positive allometry in both males (in forceps width) and females (in forceps length).

Associate Professor Konuma explained that this finding suggests female earwigs may have evolved their forceps as effective weapons in competing for mates. A previous behavioral study had shown that female earwigs engage in competition with each other for small, non-aggressive males. This new research highlights the importance of considering female traits when studying the evolution of insect morphologies.

These groundbreaking findings demonstrate how the complex and fascinating world of insects can continue to surprise us, revealing the intricacies of natural selection and mate competition.

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Biochemistry Research

Unlocking Nature’s Secrets: Scientists Discover Natural Cancer-Fighting Sugar in Sea Cucumbers

Sea cucumbers, long known for cleaning the ocean floor, may also harbor a powerful cancer-fighting secret. Scientists discovered a unique sugar in these marine creatures that can block Sulf-2, an enzyme that cancer cells use to spread. Unlike traditional medications, this compound doesn t cause dangerous blood clotting issues and offers a cleaner, potentially more sustainable way to develop carbohydrate-based drugs if scientists can find a way to synthesize it in the lab.

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Unlocking Nature’s Secrets: Scientists Discover Natural Cancer-Fighting Sugar in Sea Cucumbers

In a groundbreaking study, researchers from the University of Mississippi and Georgetown University have discovered a natural sugar compound found in sea cucumbers that can effectively block Sulf-2, an enzyme crucial for cancer growth. This breakthrough has significant implications for the development of new cancer therapies.

The research team, led by Marwa Farrag, a fourth-year doctoral candidate in the UM Department of BioMolecular Sciences, worked tirelessly to isolate and study the sugar compound, fucosylated chondroitin sulfate, from the sea cucumber Holothuria floridana. This unique sugar is not commonly found in other organisms, making it an exciting area of research.

Human cells are covered in tiny, hairlike structures called glycans that help with cell communication, immune responses, and the recognition of threats such as pathogens. Cancer cells alter the expression of certain enzymes, including Sulf-2, which modifies the structure of glycans, helping cancer spread. By inhibiting this enzyme, researchers believe they can effectively fight against the spread of cancer.

Using both computer modeling and laboratory testing, the research team found that the sugar compound from sea cucumbers can effectively inhibit Sulf-2, a promising step towards developing new cancer therapies. This natural source is particularly appealing as it does not carry the risk of transferring viruses and other harmful agents, unlike extracting carbohydrate-based drugs from pigs or other land mammals.

While this discovery holds great promise, the researchers acknowledge that further study is needed to develop a viable treatment. One of the challenges lies in finding a way to synthesize the sugar compound for future testing. The interdisciplinary nature of the scientific study highlights the importance of cross-disciplinary collaboration in tackling complex diseases like cancer.

This groundbreaking research has far-reaching implications for the medical field and demonstrates the power of scientific discovery in unlocking nature’s secrets. As researchers continue to explore this area, they may uncover new therapies that can effectively combat cancer, ultimately saving lives and improving patient outcomes.

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Air Quality

Unlocking the Secrets of Environmental DNA: A Powerful Tool for Wildlife and Human Surveillance

Environmental DNA from the air, captured with simple air filters, can track everything from illegal drugs to the wildlife it was originally designed to study.

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Dublin, a city known for its warm welcome and lively traditional music, has an unsuspecting secret – the air is teeming with DNA from various species. From cannabis to bobcats, even magic mushrooms – at least their DNA – are floating on the breeze. A new study reveals that this phenomenon can be leveraged to track wildlife, viruses, and other substances in unprecedented ways.

David Duffy, Ph.D., a professor of wildlife disease genomics at the University of Florida, has developed innovative methods for deciphering environmental DNA (eDNA). His lab has been studying sea turtle genetics using eDNA from water samples. Expanding on this research, they’ve created tools to study every species – including humans – from DNA captured in environmental samples like air filters.

“What we’re finding is that you can get intact large fragments of DNA from the air,” Duffy said. “That means you can study species without directly having to disturb them.” This approach opens up vast possibilities for tracking all species in an area simultaneously, from microbes and viruses to vertebrates like bobcats and humans.

A proof-of-concept experiment demonstrated that researchers could pick up signs of hundreds of different human pathogens from the Dublin air, including viruses and bacteria. This surveillance method can aid scientists in tracking emerging diseases. Additionally, it can track common allergens, such as peanut or pollen, more precisely than current methods allow.

In another test, Duffy’s lab identified the origin of bobcats and spiders whose DNA was collected from air filters in a Florida forest. This technique allows researchers to track endangered species without having to lay eyes on them or gather scat samples – all while knowing their exact origin is crucial for conservation efforts.

This powerful analysis is paired with impressive speed and efficiency, as demonstrated by the team’s ability to process DNA for every species in as little as a day using compact, affordable equipment, and software hosted in the cloud. This quick turnaround is orders of magnitude faster than was possible just a few years ago, making advanced environmental studies more accessible to scientists worldwide.

However, Duffy and his collaborators have called for ethical guardrails due to the potential for sensitive human genetic data to be identified using these tools.

“It seems like science fiction, but it’s becoming science fact,” Duffy said. “The technology is finally matching the scale of environmental problems.” As researchers continue to explore the capabilities of eDNA, they must also address the challenges and implications of this rapidly developing field.

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