The Mystery of Prions
More Than 30 Years Since Their Discovery, Prions Still fascinate, terrify and mystify us
Figuring out what they were was just the beginning of a field of research into prions and prion diseases that’s still growing
By Kat Eschner
October 6, 2017
Prions–the name comes from “proteinaceous infectious particle”–were big news in the 1980s, when it became clear that these proteins caused disease. But more than 30 years after they were discovered, we’re still figuring them out.
On October 6th in 1997, American biologist Stanley B. Prusiner received the Nobel Prize in medicine for his discovery of prions, “an entirely new genre of disease-causing agents,” in the words of the Nobel committee. But even though Prusiner’s work started in 1972, by 2017 we still only sort of understand prions.
You’ve probably heard of these infectious proteins in the context of brain diseases like mad cow disease (technical name: bovine spongiform encephalopathy). Humans can also get prion diseases, such as Creutzfeldt-Jacob disease and the rare Kuru, which was transmitted by the Fore people’s custom of eating their deceased as part of funerary rituals. These diseases, which are collectively known as transmissible spongiform encephalopathies, are only the best-understood part of the prion picture.
“Prions are distorted versions of normal proteins found in human and animal brain and other tissues,” explains Colorado State University’s Prion Research Center. “These distorted (‘misfolded’) proteins damage brain cells, leading to fatal dementias akin to human Alzheimer’s and Parkinson’s diseases.”
When normal proteins in your brain–for some reason that’s not fully understood–misfold, “they turn into contagious pathogens that recruit any other prions they come into contact with, grouping together in clumps that damage other cells and eventually cause the brain itself to break down,” writes Fiona MacDonald for ScienceAlert.
“…Technically speaking, proteins shouldn’t be able to infect other proteins–they’re not alive, after all–and scientists have never really been able to explain the behaviour of prions–hence their reputation as the weirdest molecules ever,” she writes.
Not only are prions not alive (and contain no DNA), they can survive being boiled, being treated with disinfectants, and can still infect other brains years after they were transferred to a scalpel or other tool.
We’re still trying to figure out how normal proteins fold into prions and what causes them to do so, although there have been a number of advances in recent years. Among them, Alzheimer’s and Parkinson’s have recently been linked to prions. Scientists have suggested that these brain diseases are caused by similar protein folding and it has been suggested that they should be called “prionoid” diseases–similiar to TSEs, but not transmissible (that we know of.)
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