Difference between revisions of "Prion"
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| − | ''For the bird, see [[Prion (bird)]]. | + | ''For the bird, see [[Prion (bird)]]. For the protein, see [[PrP]]. this is a comment until I make the page'' |
| − | Prions are misfolded proteins with the ability to transmit their misfolded shape onto normal variants of the same protein. They characterize several fatal and transmissible neurodegenerative diseases in humans and many other animals. It is not known what causes the normal protein to misfold, but the abnormal three-dimensional structure is suspected of conferring infectious properties, collapsing nearby protein molecules into the same shape. The word prion derives from "proteinaceous infectious particle". Prion forms of [[PrP]] are responsible for [[Transmissible spongiform encephalopathy|transmissible spongiform encephalopathies]], and prion forms of amyloid-beta and tau proteins cause [[Alzheimer's disease]]. | + | Prions are misfolded proteins with the ability to transmit their misfolded shape onto normal variants of the same protein. They characterize several fatal and transmissible neurodegenerative diseases in humans and many other animals. It is not known what causes the normal protein to misfold, but the abnormal three-dimensional structure is suspected of conferring infectious properties, collapsing nearby protein molecules into the same shape. The word prion derives from "proteinaceous infectious particle". Prion forms of [[PrP]] are responsible for [[Transmissible spongiform encephalopathy|transmissible spongiform encephalopathies]], and prion forms of amyloid-beta and tau proteins cause [[Alzheimer's disease]]. |
The word prion, coined in 1982 by Stanley B. Prusiner, is a portmanteau derived from protein and infection, hence prion, and is short for "proteinaceous infectious particle", in reference to its ability to self-propagate and transmit its conformation to other proteins. Its main pronunciation is /ˈpriːɒn/, although /ˈpraɪɒn/, as the homographic name of the bird (prions or whalebirds) is pronounced, is also heard. In his 1982 paper introducing the term, Prusiner specified that it be "pronounced pree-on." | The word prion, coined in 1982 by Stanley B. Prusiner, is a portmanteau derived from protein and infection, hence prion, and is short for "proteinaceous infectious particle", in reference to its ability to self-propagate and transmit its conformation to other proteins. Its main pronunciation is /ˈpriːɒn/, although /ˈpraɪɒn/, as the homographic name of the bird (prions or whalebirds) is pronounced, is also heard. In his 1982 paper introducing the term, Prusiner specified that it be "pronounced pree-on." | ||
Revision as of 02:16, October 20, 2020
For the bird, see Prion (bird). For the protein, see PrP. this is a comment until I make the page
Prions are misfolded proteins with the ability to transmit their misfolded shape onto normal variants of the same protein. They characterize several fatal and transmissible neurodegenerative diseases in humans and many other animals. It is not known what causes the normal protein to misfold, but the abnormal three-dimensional structure is suspected of conferring infectious properties, collapsing nearby protein molecules into the same shape. The word prion derives from "proteinaceous infectious particle". Prion forms of PrP are responsible for transmissible spongiform encephalopathies, and prion forms of amyloid-beta and tau proteins cause Alzheimer's disease.
The word prion, coined in 1982 by Stanley B. Prusiner, is a portmanteau derived from protein and infection, hence prion, and is short for "proteinaceous infectious particle", in reference to its ability to self-propagate and transmit its conformation to other proteins. Its main pronunciation is /ˈpriːɒn/, although /ˈpraɪɒn/, as the homographic name of the bird (prions or whalebirds) is pronounced, is also heard. In his 1982 paper introducing the term, Prusiner specified that it be "pronounced pree-on."
References
https://www.hopkinsmedicine.org/health/conditions-and-diseases/prion-diseases
http://www.prionalliance.org/2013/12/02/what-are-human-prion-diseases/