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Elusive Prions Begin to Yield Secrets

Michael Smith
Reviewed by Zalman S. Agus, MD; Emeritus Professor at the University of Pennsylvania School of Medicine. | May 9, 2007
  • Explain to interested patients that prions -- misfolded proteins -- have been implicated in a range of diseases, including Creutzfeldt-Jakob disease and kuru in humans.

  • Note that this basic research study finds that small sections of the original proteins govern the switch to the prion form and also appear to explain why some prions -- such as the one involved in mad cow disease -- can jump the species barrier.

CAMBRIDGE, Mass., May 9 -- Small peptide segments -- typically only 19 amino acids in length -- govern the switch from a normal protein to a self-perpetuating infectious prion, according to researchers here.

The same regions of the protein also govern whether the resulting prion can jump from one species to another, according to Susan Lindquist, Ph.D., of the Whitehead Institute for Biomedical Research.

The finding may shed new light on the development and transmission of prion-related disorders, such as bovine spongiform encephalopathy, the so-called mad-cow disease, Dr. Lindquist and Peter Tessier, Ph.D., reported online in Nature.

Bovine spongiform encephalopathy is a prion disease that affects cattle, but was apparently transmitted to humans in what is now called variant Creutzfeldt-Jakob disease. About one in a million people yearly is affected by the sporadic human form of Creutzfeldt-Jakob disease.

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