Scientists have identified the protein that helps poison dart frogs safely accumulate their namesake toxins, according to a study published today in eLife.
The findings solve a long-standing scientific mystery and may suggest potential therapeutic strategies for treating humans poisoned with similar molecules.
Alkaloid compounds, such as caffeine, make coffee, tea and chocolate delicious and pleasant to consume, but can be harmful in large amounts. In humans, the liver can safely metabolise modest amounts of these compounds. Tiny poison dart frogs consume far more toxic alkaloids in their diets, but instead of breaking the toxins down, they accumulate them in their skin as a defence mechanism against predators.
“It has long been a mystery how poison dart frogs can transport highly toxic alkaloids around their bodies without poisoning themselves,” says lead author Aurora Alvarez-Buylla, a PhD student in the Biology Department at Stanford University in California, US. “We aimed to answer this question by looking for proteins that might bind and safely transport alkaloids in the blood of poison frogs.”
Alvarez-Buylla and her colleagues used a compound similar to the poison frog alkaloid as a kind of ‘molecular fishing hook’ to attract and bind proteins in blood samples taken from the Diablito poison frog. The alkaloid-like compound was bioengineered to glow under fluorescent light, allowing the team to see the proteins as they bound to this decoy.
Next, they separated the proteins to see how each one interacted with alkaloids in a solution. They discovered that a protein called alkaloid binding globulin (ABG) acts like a ‘toxin sponge’ that collects alkaloids. They also identified how the protein binds to alkaloids by systematically testing which parts of the protein were needed to bind it successfully.
“The way that ABG binds alkaloids has similarities to the way proteins that transport hormones in human blood bind their targets,” Alvarez-Buylla explains. “This discovery may suggest that the frog’s hormone-handling proteins have evolved the ability to manage alkaloid toxins.”
The authors say the similarities with human hormone-transporting proteins could provide a starting point for scientists to try and bioengineer human proteins that can ‘sponge up’ toxins. “If such efforts are successful, this could offer a new way to treat certain kinds of poisonings,” says senior author Lauren O’Connell, Assistant Professor in the Department of Biology, and a member of the Wu Tsai Neurosciences Institute, at Stanford University.
“Beyond potential medical relevance, we have achieved a molecular understanding of a fundamental part of poison frog biology, which will be important for future work on the biodiversity and evolution of chemical defences in nature,” O’Connell concludes.
Media contacts
Emily Packer
eLife
e.packer@elifesciences.org
+441223855373George Litchfield
eLife
g.litchfield@elifesciences.org
About
eLife transforms research communication to create a future where a diverse, global community of scientists and researchers produces open and trusted results for the benefit of all. Independent, not-for-profit and supported by funders, we improve the way science is practised and shared. In support of our goal, we have launched a new publishing model that ends the accept/reject decision after peer review. Instead, papers invited for review will be published as a Reviewed Preprint that contains public peer reviews and an eLife assessment. We also continue to publish research that was accepted after peer review as part of our traditional process. eLife receives financial support and strategic guidance from the Howard Hughes Medical Institute, Knut and Alice Wallenberg Foundation, the Max Planck Society and Wellcome. Learn more at https://elifesciences.org/about.
To read the latest Biochemistry and Chemical Biology research published in eLife, visit https://elifesciences.org/subjects/biochemistry-chemical-biology.
And for the latest in Ecology, see https://elifesciences.org/subjects/ecology.