Yale Researchers Find Hope for Safe and Novel Painkillers from Tarantula Venom

Peruvian Green Velvet Tarantula

Yale researchers find new hope for safe and novel painkillers from the venom of the Peruvian green velvet tarantula.

Screening more than 100 spider toxins, Yale researchers identified a protein from the venom of the Peruvian green velvet tarantula that blunts activity in pain-transmitting neurons. The findings, reported in the March 3 issue of the journal Current Biology, show the new screening method used by the scientists has the potential to search millions of different spider toxins for safe pain-killing drugs and therapies.

The researchers note that they tested the spider toxins on only one of a dozen suspected human pain channels.

“The likelihood is that within the vast diversity of spider toxins we will find others that are active against other channels important for pain,” said Michael Nitabach, associate professor of cellular and molecular physiology and of genetics, and senior author of the paper.

The researchers screened the toxins from a variety of tarantula species to find one that blocked TRPA1, an ion channel on the surface of pain-sensing neurons that is implicated in inflammation and neuropathic pain.

In a process dubbed toxineering by the Yale researchers, the team generated another small library of mutated versions of the tarantula toxin to find one that blocked TRPA1 but had no effect on activity of other channels on the surface of neurons.

“The beauty of the system is we can also screen engineered toxins not found in nature, and identify higher-potency and more specific molecular variants that lack deleterious effects on essential nerve functions,’’ Nitabach said.

His lab plans to ramp up efforts to test tens of thousands of new toxins for similar biological activity against pain-sensing neurons.

Junhong Gui and Boyi Liu of Yale are co-lead authors of the study, which was funded by the National Institutes of Health.

Publication: Junhong Gui, et al., “A Tarantula-Venom Peptide Antagonizes the TRPA1 Nociceptor Ion Channel by Binding to the S1–S4 Gating Domain,” Current Biology, 2014; DOI:10.1016/j.cub.2014.01.013

Source: Bill Hathaway, Yale News

Image: Yale News

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