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Tarantula Venom Protein May Hold Promise as Alternative to Opioid Pain Killers
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Tarantula Venom Protein May Hold Promise as Alternative to Opioid Pain Killers

Tarantula Venom Protein May Hold Promise as Alternative to Opioid Pain Killers
News

Tarantula Venom Protein May Hold Promise as Alternative to Opioid Pain Killers

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Molecules in tarantula venom could be used as an alternative to opioid pain killers for people seeking chronic pain relief.

Institute for Molecular Bioscence researchers have designed a new tarantula venom mini-protein that can potentially relieve severe pain without addiction.

Dr Christina Schroeder said the current opioid crisis around the world meant urgent alternatives to morphine and morphine-like drugs, such as fentanyl and oxycodone, were desperately needed.


“Although opioids are effective in producing pain relief, they come with unwanted side-effects like nausea, constipation and the risk of addiction, placing a huge burden on society," - Dr Schroeder.
“Our study found that a mini-protein in tarantula venom from the Chinese bird spider, known as Huwentoxin-IV, binds to pain receptors in the body.

“By using a three-pronged approach in our drug design that incorporates the mini-protein, its receptor and the surrounding membrane from the spider venom, we’ve altered this mini-protein resulting in greater potency and specificity for specific pain receptors.

“This ensures that just the right amount of the mini-protein attaches itself to the receptor and the cell membrane surrounding the pain receptors.”

Dr Schroeder said the mini-protein had been tested in mouse models and shown to work effectively.

“Our findings could potentially lead to an alternative method of treating pain without the side-effects and reduce many individuals’ reliance on opioids for pain relief,” she said.

Reference: Agwa, et al.  (2020) Manipulation of a spider peptide toxin alters its affinity for lipid bilayers and potency and selectivity for voltage-gated sodium channel subtype 1.7. The Journal of Biological Chemistry. DOI: 10.1074/jbc.RA119.012281

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