Scientists have pioneered a groundbreaking method to combat snake venom using newly designed proteins, offering hope for more effective, accessible, and affordable antivenom solutions.
By utilizing advanced computational techniques and deep learning, this innovative approach has already shown promising results in neutralizing deadly toxins, potentially transforming antivenom development, and offering new strategies for tackling other neglected diseases.
Breakthrough in Antivenom Research
Scientists have designed new proteins — unlike any found in nature — that can neutralize some of the most toxic components of snake venom. Using advanced deep learning and computational methods, researchers have developed these proteins with the potential to create safer, more affordable, and widely accessible treatments compared to existing antivenoms.
Each year, over 2 million people suffer from snakebites, with more than 100,000 deaths and 300,000 cases of severe complications, including limb deformities, amputations, and other long-term disabilities, according to the World Health Organization. The highest burden of snakebites is seen in regions such as Sub-Saharan Africa, South Asia, Papua New Guinea, and Latin America, where access to effective treatment is often limited.
Advancements in Computational Biology
This groundbreaking computational biology research, aimed at improving antivenom therapies, was led by scientists from the UW Medicine Institute for Protein Design and the Technical University of Denmark. Their findings were published in Nature on January 15.
The lead author of the paper is Susana Vazquez Torres of the Department of Biochemistry at the UW School of Medicine and the UW Graduate Program in Biological Physics. Her hometown is Querétaro, Mexico, which is located near viper and rattlesnake habitats. Her professional goal is to invent new drugs for neglected diseases and injuries, including snakebites.

The Challenge of Elapid Snakebites
Her research team, which also included international experts in snakebite research, drugs and diagnostics, and tropical medicine from the United Kingdom and Denmark, concentrated their attention on finding ways to neutralize venom gathered from certain elapids. Elapids are a large group of poisonous snakes, among them cobras and mambas, that live in the tropics and subtropics.
Most elapid species have two small fangs shaped like shallow needles. During a tenacious bite, the fangs can inject venom from glands at the back of the snake's jaw. Among the venom's components are potentially lethal three-finger toxins. These chemicals damage bodily tissues by killing cells. More seriously, by interrupting signals between nerves and muscles, three-finger toxins can cause paralysis and death.
Limitations of Current Treatments
At present, venomous snakebites from elapids are treated with antibodies taken from the plasma of animals that have been immunized against the snake toxin. Producing the antibodies is costly, and they have limited effectiveness against three-finger toxins. This treatment can also have serious side effects, including causing the patient to go into shock or respiratory distress.
"Efforts to try to develop new drugs have been slow and laborious," noted Vazquez Torres.
Innovations in Protein Design
The researchers used deep learning computational methods to try to speed the discovery of better treatments. They created new proteins that interfered with the neurotoxic and cell-destroying properties of the three-finger toxin chemicals by binding with them.
Through experimental screening, the scientists obtained designs that generated proteins with thermal stability and high binding affinity. The actual synthesized proteins were almost a complete match at the atomic level with the deep-learning computer design.
In lab dishes, the designed proteins effectively neutralized all three of the subfamilies of three-finger toxins tested. When given to mice, the designed proteins protected the animals from what could have been a lethal neurotoxin exposure.
Promising Results and Future Directions
Designed proteins have key advantages. They could be manufactured with consistent quality through recombinant DNA technologies instead of by immunizing animals. (Recombinant DNA technologies in this case refer to the lab methods the scientists employed to take a computationally designed blueprint for a new protein and synthesize that protein.)
Also, the new proteins designed against snake toxins are small, compared to antibodies. Their smaller size might allow for greater penetration into tissues to quickly counteract the toxins and reduce damage.
Expanding the Potential of Computational Design
In addition to opening new avenues to develop antivenoms, the researchers think computational design methods could be used to develop other antidotes. Such methods also might be used to discover medications for undertreated illnesses that affect countries with significantly limited scientific research resources.
"Computational design methodology could substantially reduce the costs and resource requirements for development of therapies for neglected tropical diseases," the researchers noted.
Explore Further: AI Triumphs Over Venom: Revolutionary Snakebite Antidotes Unveiled
Reference: "De novo designed proteins neutralize lethal snake venom toxins" by Susana Vázquez Torres, Melisa Benard Valle, Stephen P. Mackessy, Stefanie K. Menzies, Nicholas R. Casewell, Shirin Ahmadi, Nick J. Burlet, Edin Muratspahić, Isaac Sappington, Max D. Overath, Esperanza Rivera-de-Torre, Jann Ledergerber, Andreas H. Laustsen, Kim Boddum, Asim K. Bera, Alex Kang, Evans Brackenbrough, Iara A. Cardoso, Edouard P. Crittenden, Rebecca J. Edge, Justin Decarreau, Robert J. Ragotte, Arvind S. Pillai, Mohamad Abedi, Hannah L. Han, Stacey R. Gerben, Analisa Murray, Rebecca Skotheim, Lynda Stuart, Lance Stewart, Thomas J. A. Fryer, Timothy P. Jenkins and David Baker, 15 January 2025, Nature.
DOI: 10.1038/s41586-024-08393-x
The senior researchers on the project to design protein treatments for elapid snakebites were Timothy J. Perkins at the Technical University of Denmark and David Baker of the UW Medicine Institute for Protein Design and the Howard Hughes Medical Institute. Baker is a professor of biochemistry at the UW School of Medicine.
The University of Washington has submitted a provisional U.S. patent application for the design and composition of the proteins created in this study.
News
Scientists Just Overturned a 100-Year-Old Belief About Bacteria in the Lungs
New findings raise questions about the role of microbes living in the lungs. More than 35 trillion bacteria live throughout the human body, forming microbiomes in the gut, mouth, lungs, skin, and urogenital tract. [...]
GHCE Concept
From the preface of the book Global Health Care Equivalency in the Age of Nanotechnology, Nanomedicine and Artificial Intelligence, Edited by Frank Boehm: Since the publication of my first book (Nanomedical Device and Systems [...]
Novartis, Ionis drug failure spurs questions
Pelacarsen didn’t protect heart health despite lowering levels of a protein particle, “Lp(a),” in a large clinical trial — a result with important implications for cardiovascular drug research. Dive Brief: An RNA drug from [...]
New injectable treatment helps the brain rebuild after stroke
Biomedical engineers at Duke University have created an injectable biomaterial that may help the brain recover from damage left behind by an ischemic stroke. In experiments with mice, the material transformed the cavity created [...]
Scientists Discover a Hidden “Immune Organ” Inside the Skull
Researchers discovered lymph node-like immune hubs inside skull bone marrow that appear to act as rapid-response centers for the brain. For decades, the brain was thought to operate largely apart from the immune system. [...]
Engineered tRNAs and lipid nanoparticles target nonsense mutation cystic fibrosis
Researchers have developed a potential new approach for treating a form of cystic fibrosis caused by so-called nonsense mutations, combining chemically modified transfer RNAs with lipid nanoparticles designed to deliver the therapy directly to [...]
New pancreatic cancer drug carries a $39,800 monthly list price
A groundbreaking treatment for one of the most common forms of pancreatic cancer has been approved in pill form by the FDA. Revolution Medicines’ oral tablet daraxonrasib, branded as Rasonque, reduced the risk of [...]
Researchers Have Discovered a New Way To Reduce Chronic Nerve Pain
A cancer-linked protein called BRAF may help drive chronic nerve pain, and existing cancer drugs targeting it reduced pain sensitivity in preclinical models. Chronic nerve pain can persist long after an injury and often [...]
Our books now available worldwide!
Online Sellers other than Amazon, Routledge, and IOPP Indigo Global Health Care Equivalency in the Age of Nanotechnology, Nanomedicine and Artifcial Intelligence Global Health Care Equivalency In The Age Of Nanotechnology, Nanomedicine And Artificial [...]
Quantum-Enabled Regenerative Health: Reimagining Wellness, Precision Health and Longevity Medicine
Introduction Healthcare is approaching a frontier where the quantum portfolio could influence not only how disease is diagnosed and treated, but how health itself is measured, modeled, predicted and preserved. Quantum computing, quantum simulation, [...]
FDA Clears First-of-Its-Kind Nonmedication Treatment for PTSD
The FDA has cleared a system that uses brain activity data to personalize magnetic stimulation for PTSD, adding a new nonmedication treatment option. Every day in the United States, approximately 17.5 veterans die by suicide, [...]
FDA approves breakthrough drug to treat advanced pancreatic cancer
The Food and Drug Administration (FDA) approved on Wednesday a drug that could extend the survival of those with metastatic pancreatic cancer. The drug, called daraxonrasib, will be sold under the brand name Rasonque [...]
AI Decodes a Hidden DNA Signal Linked to Disease-Causing Mutations
Machine learning identifies the likely “initiator” and enables new predictions about DNA mutations that can cause disease. Every human cell depends on tens of thousands of genes being switched on at the right time [...]
Pope Leo Urges Global Response to Congo’s Deadliest Ebola Outbreak
Pope Leo called for international action to address the Ebola outbreak in the Democratic Republic of Congo. The epidemic has claimed over 2,500 lives and is the nation's largest recorded outbreak. The Pope emphasized [...]
Is there a summer COVID-19 surge this year? Yep, it’s ramping up again
Hantavirus. Ebola. West Nile. Measles. And, of course, cyclospora — that stomach parasite making people miserable across the country. Americans have plenty to worry about this summer. But remember COVID-19? It may not be [...]
Natural Compound in Broccoli Could Help Treat a Rare, Incurable Neurological Disease
Swinburne researchers have discovered how broccoli could help treat an extremely rare and incurable disease that affects only about 200 Australians. A naturally occurring compound in broccoli is being investigated as a possible treatment [...]















