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n2doc

(47,953 posts)
Wed Jan 8, 2014, 09:50 AM Jan 2014

The Bright Side of Prions

By Randal Halfmann
In Kurt Vonnegut’s Cat’s Cradle, scientists create a highly stable form of crystalline water called “ice-nine” that stays frozen even at high temperatures. Ice-nine instantly freezes any liquid water it touches. Its accidental release into nature solidifies the oceans and all contiguous bodies of water, and global catastrophe threatens our existence. Luckily for us, ice-nine is fictitious. But its biological counterpart, unfortunately, is not. The misfolded proteins known as prions are very real.

Prions are proteinaceous infectious particles, formed when normal proteins misfold and clump together. Biochemists Byron Caughey of the National Institute of Allergy and Infectious Diseases and Peter Lansbury of Brigham and Women’s Hospital were among the first to explore the analogy between Vonnegut’s ice-nine and prions in their 1995 review of scrapie, an infectious and deadly neurological disease of sheep.1 Like ice-nine, the particles that spread scrapie consist of highly stable crystals of a normally innocuous material found in the brains of sheep. Crystalline clumps of a misfolded version of this protein coax other molecules of the same protein to fold into the aberrant conformation. The process continues until virtually all of that protein in a cell or tissue has been converted to prions. In the case of scrapie and other mammalian prion diseases, the consequence of this self-amplifying cycle is an accumulation of toxic clumps of proteins that destroys neurons and invariably kills the organism.

The chilling similarity between the modus operandi of ice-nine and prions is an apt illustration of the long-standing and well-deserved reputation of prions as catastrophic agents. Researchers are identifying more and more cases of prion-like protein misfolding that cause neurodegenerative diseases.

But a different side of prions is also coming to light. Many newly discovered prions and prion-like proteins do not appear to cause disease at all. On the contrary, some even protect against it. Still other prions are turning out to be key players in basic biological processes. (See illustration.) These discoveries are driving a new appreciation for prions as versatile components in the machinery of life, a paradigm that has fostered conceptual advances in fields as diverse as signal transduction, memory formation, and evolution.

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http://www.the-scientist.com/?articles.view/articleNo/38721/title/The-Bright-Side-of-Prions/

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siligut

(12,272 posts)
2. "Since prions are composed of amyloids, are these amyloid diseases also, in effect prion diseases?"
Wed Jan 8, 2014, 12:20 PM
Jan 2014
Large numbers of neurofibrillary tangles (NFTs) and amyloid plaques are diagnostic markers for Alzheimer disease (AD), but lesser numbers of these lesions are also seen in nondemented elderly individuals. Much of the existing literature suggests that the NFTs of AD have a closer correlation with cognitive function than do amyloid plaques. Whether a similar relationship exists in normal aging and mild cognitive impairment (MCI), a condition that frequently reflects a preclinical stage of AD, remains unknown.

http://www.ncbi.nlm.nih.gov/pubmed/12756137


In Alzheimer's a complex of structures/functions go awry, but tau protein and beta amyloid plaque formation appear to be the initiating factors. I wonder too is it possible that it is prions that cause the tau protein to undergo phosphorylation? So then is it possible to create a vaccine against those prions?

Gothmog

(145,176 posts)
3. I have an aunt who died due to Creutzfeldt-Jakob
Wed Jan 8, 2014, 01:03 PM
Jan 2014

I have reading up on this disease and this article is interesting.

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