"Our discovery could be used to design new medicines", says Pål Stenmark, Associate Professor at the Department of Biochemistry and Biophysics, Stockholm University.
Dr Stenmark and his research team have determined the three-dimensional structure of the entire tetanus toxin protein.
"We can now see the exact positions of the 20 000 atoms that build up the tetanus toxin. It means that we can see how both the toxin and vaccine actually look. Botulinum neurotoxins and the tetanus toxin are the deadliest toxins known to man. The toxins are large proteins that are made by specialised bacteria. The bacteria that produce the tetanus toxin are found in common soil and flourish in untended wounds. One unusual feature of the tetanus toxin is that it travels in nerve cells to the spinal cord from where it can cause life-threatening cramping and spasms."
These start with the shorter nerves in the face (lockjaw) and move on to cause spasms violent enough to break bones.
"We discovered that the poison takes on different forms depending on pH – it appears one way in acidic liquids and very different in a neutral pH environment. We believe that this is important for the toxins ability to move from the wound to the spinal cord and to adapt to different environments. Before this research, no one knew what the toxin looked like or that it changed structure depending on pH."
Pål Stenmark's research group also studies the botulinum neurotoxins, which are similar to the tetanus toxin, but causes paralysis instead of spasms and cramping.
"We want to know more about why these two poisons have nearly opposite effects – tetanus toxin travels through nerve cells to the spinal cord and cause severe muscle cramps whereas the botulinum neurotoxin stays put and causes paralysis. Our findings could be useful in creating new medicines that could be transported to the brain", says Pål Stenmark.
"People are not vaccinated against tetanus in many parts of the world, and infants and new mothers are particularly at risk. Large international vaccination programs have dramatically improved the situation, but tens of thousands of people still die of tetanus every year."
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The article
"The structure of the tetanus toxin reveals pH-mediated domain dynamics" by Dr Geoffrey Masuyer, Dr Julian Conrad and Dr Pål Stenmark is published in EMBO Reports.
Link: http://embor.embopress.org/cgi/doi/10.15252/embr.201744198
Contact
For more information, please contact Pål Stenmark at: 46-8-16 37 29 or 46-739-84 12 16, [email protected]
Photo
Geoffrey Masuyer och Pål Stenmark
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http://www.su.se/english
http://dx.doi.org/10.15252/embr.201744198
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Story Source: Materials provided by Scienmag
