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Animals

Revolutionizing Drug Development with Minimal Mice: A Breakthrough in Antibody Testing

New active ingredients such as antibodies are usually tested individually in laboratory animals. Researchers have now developed a technology that can be used to test around 25 antibodies simultaneously in a single mouse. This should not only speed up the research and development pipeline for new drugs, but also hugely reduce the number of laboratory animals required.

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The development of new drugs is a complex process that requires extensive testing on animals before they can be approved for human use. Researchers at the University of Zurich have made a groundbreaking discovery that could significantly reduce the number of laboratory animals required in this process.

The team, led by Markus Seeger from the Institute of Medical Microbiology and Johannes vom Berg from the Institute of Laboratory Animal Science, has developed a technology that allows them to test up to 25 antibodies simultaneously in a single mouse. This innovation is set to speed up the research and development pipeline for new drugs while also reducing the number of laboratory animals required.

Antibodies are proteins that specifically bind to certain structures on cells or molecules. They are used in many modern medicines, including treatments for cancer, autoimmune diseases, and infectious diseases. However, testing antibodies individually in animal models is a time-consuming process that requires a large number of laboratory animals.

The new technology uses protein fragments called flycodes to mark each antibody individually. These flycodes act as barcodes, allowing researchers to separate and analyze the individual antibodies from a complex mixture. The results show that this method delivers high-quality preclinical data on the investigated antibodies, reducing the need for multiple animal tests.

One of the most significant advantages of this technology is its potential to reduce the number of laboratory animals required in drug development. According to the researchers, this new method could reduce the number of animals required by a factor of up to 100. This not only speeds up the research and development process but also contributes to reducing animal suffering.

The researchers demonstrated that their flycode technology does not compromise the efficacy of the antibodies in living organisms. They tested the antibodies against cancer cells, and the targeted accumulation worked correctly even when combined with other antibodies. The team also used flycodes to analyze the properties and data for a series of 80 drug-like synthetic biomolecules, known as sybodies.

The breakthrough has significant implications for the pharmaceutical industry, where preclinical tests account for a large proportion of animals used. By reducing the number of animal tests required, this technology can advance preclinical discovery pipelines more efficiently in the future.

Animals

Unveiling the Ancient Secrets of the Dirt Ant: A 16-million-year-old Fossil Reveals the Smallest Predator Ant Ever Found

A fossilized Caribbean dirt ant, Basiceros enana, preserved in Dominican amber, reveals the species ancient range and overturns assumptions about its size evolution. Advanced imaging shows it already had the camouflage adaptations of modern relatives, offering new insights into extinction and survival strategies.

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A team of researchers led by the New Jersey Institute of Technology (NJIT) has made a groundbreaking discovery in the field of entomology. A 16-million-year-old amber fossil, found in the Dominican Republic, has revealed the smallest predator ant ever discovered. The fossil, named Basiceros enana, belongs to the Basiceros genus of dirt ants, which are known for their remarkable ability to camouflage themselves in soil and leaf litter using specialized hairs on their bodies.

Until now, these ants had only been found in the neotropical rainforests stretching from Costa Rica to Southern Brazil. However, this ancient fossil suggests that they once inhabited the Caribbean islands as well. The discovery raises new questions about how these ants reached their present-day habitats and why they ultimately went extinct in the region.

The researchers applied advanced imaging techniques at NJIT and Japan’s Okinawa Institute of Science and Technology Graduate University to capture the fossil in exquisite detail. By comparing the specimen’s physical characteristics with those of all known modern dirt ant species, they conducted molecular dating analyses to trace its evolutionary lineage.

Measuring just 5.13 millimeters long, Basiceros enana is significantly smaller than its modern relatives, which can reach nearly 9 millimeters in length. This finding flips previous hypotheses that these ants were ancestrally large and shrank over time. Instead, it suggests that they almost doubled in size over the course of 20 million years.

The fossil also preserves other distinctive morphological characteristics, such as an upturned propodeal spine, a trapezoid-like head structure, and predatory features like mandibles with 12 triangular teeth. These adaptations, including two layers of specialized hairs for adhering soil particles against their bodies, suggest that the ancient Caribbean dirt ants employed the same strategies to avoid predators and prey that modern Basiceros ants use today.

Despite these remarkable findings, the researchers note that the extinction of these ancient ants in the region remains a mystery. They propose that it may have been due to a loss of available niches or interspecific competition, highlighting the importance of understanding what drives local extinctions to mitigate modern human-driven extinction and protect biodiversity.

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Animals

Nature’s Anti-Aging Hack? Jewel Wasp Larvae Slow Their Biological Clock

Scientists discovered that jewel wasp larvae that undergo a developmental “pause” live longer and age more slowly at the molecular level by nearly 30%. This slowdown is tied to conserved biological pathways, hinting at possible applications for human aging.

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The discovery by scientists at the University of Leicester has revealed that jewel wasps can undergo a natural “time-out” as larvae before emerging into adulthood with this surprising advantage. The study, published in PNAS, shows that this pause in development within the wasp dramatically extends lifespan and decelerates the ticking of the so-called “epigenetic clock” that marks molecular aging.

Aging isn’t just about counting birthdays; it’s also a biological process that leaves molecular fingerprints on our DNA. One of the most accurate markers of this process is the epigenetic clock, which tracks chemical changes in DNA, known as methylation, that accumulate with age. The study found that by altering the course of development itself, the jewel wasps could slow down their aging process at a molecular level.

To investigate this phenomenon, a team of researchers exposed jewel wasp mothers to cold and darkness, triggering a hibernation-like state in their babies called diapause. This natural “pause button” extended the offsprings’ adult lifespan by over a third. Even more remarkably, the wasps that had gone through diapause aged 29% more slowly at the molecular level than their counterparts.

“It’s like the wasps who took a break early in life came back with extra time in the bank,” said Evolutionary Biology Professor Eamonn Mallon, senior author on the study. “It shows that aging isn’t set in stone; it can be slowed by the environment, even before adulthood begins.”

The researchers found that this molecular slowdown was linked to changes in key biological pathways that are conserved across species, including those involved in insulin and nutrient sensing. These same pathways are being targeted by anti-aging interventions in humans.

What makes this study novel and surprising is that it demonstrates a long-lasting, environmentally triggered slowdown of aging in a system that’s both simple and relevant to human biology. It offers compelling evidence that early life events can leave lasting marks not just on health but on the pace of biological aging itself.

Understanding how and why aging happens is a major scientific challenge. This study opens up new avenues for research, not just into the biology of wasps, but into the broader question of whether we might one day design interventions to slow aging at its molecular roots. With its genetic tools, measurable aging markers, and clear link between development and lifespan, Nasonia vitripennis is now a rising star in aging research.

“In short, this tiny wasp may hold big answers to how we can press pause on aging,” concluded Professor Mallon. Funding for the study was provided by The Leverhulme Trust and The Biotechnology and Biological Sciences Research Council (BBSRC).

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Animals

“Nature’s Armor: Scientists Uncover Gene Behind Aussie Skinks’ Immunity to Deadly Snake Venom”

Australian skinks have developed a remarkable genetic defense against venomous snake bites by mutating a key muscle receptor, making them resistant to neurotoxins. These tiny but powerful molecular changes mirror those found in cobra-resistant mammals like mongooses and honey badgers. This evolutionary arms race not only shows how adaptable life can be but also offers exciting possibilities for creating new antivenoms and therapies in human medicine.

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The article has been rewritten to improve clarity, structure, and style while maintaining the core ideas:

Nature’s Armor: Scientists Uncover Gene Behind Aussie Skinks’ Immunity to Deadly Snake Venom

In a groundbreaking study led by the University of Queensland, scientists have discovered the genetic secret behind Australian skinks’ remarkable ability to withstand deadly snake venom. The research, published in the International Journal of Molecular Sciences, reveals that these small lizards have evolved a molecular armor to protect themselves from the toxic effects of neurotoxins.

Professor Bryan Fry from UQ’s School of the Environment explained that the skinks’ defense mechanism involves tiny changes in a critical muscle receptor called the nicotinic acetylcholine receptor. This receptor is normally targeted by snake venom, which blocks nerve-muscle communication and leads to rapid paralysis and death. However, in a stunning example of evolutionary adaptation, researchers found that skinks independently developed mutations on 25 occasions to block venom from attaching.

“It’s a testament to the massive evolutionary pressure exerted by venomous snakes after their arrival and spread across the Australian continent,” Professor Fry said. “The same mutations evolved in other animals like mongooses, which feed on cobras.”

Researchers confirmed that Australia’s Major Skink (Bellatorias frerei) has developed exactly the same resistance mutation as the honey badger, famous for its immunity to cobra venom.

To validate these findings, scientists conducted functional testing at UQ’s Adaptive Biotoxicology Laboratory. Dr. Uthpala Chandrasekara led the laboratory work and reported that the data was “crystal clear.” The modified receptors simply didn’t respond to toxins, demonstrating their remarkable ability to repel deadly snake venom.

This research has significant implications for biomedical innovation, particularly in the development of novel antivenoms or therapeutic agents. Dr. Chandrasekara emphasized that understanding how nature neutralizes venom can provide valuable clues for designing more effective treatments.

The project involved collaborations with museums across Australia and offers a promising example of interdisciplinary research, bridging the gap between scientific discovery and potential applications.

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