{"id":848,"date":"2017-09-25T16:10:24","date_gmt":"2017-09-25T10:40:24","guid":{"rendered":"https:\/\/babrone.avfu.ac.in\/blog\/?p=848"},"modified":"2018-11-12T10:14:56","modified_gmt":"2018-11-12T04:44:56","slug":"prusiners-struggle-behind-the-birth-of-prion","status":"publish","type":"post","link":"https:\/\/babrone.avfu.ac.in\/blog\/?p=848","title":{"rendered":"Prusiner\u2019s struggle behind the \u201cbirth\u201d of Prion"},"content":{"rendered":"<p style=\"text-align: justify;\"><span style=\"font-family: 'Times New Roman', serif; color: #000000;\"><span style=\"font-size: large;\">Proteinaceous Infectious Particle, commonly abbreviated as \u2018prion\u2019, is now known as the cause of a number of diseases in animals and human. The examples of such animal diseases include Scrapie in sheep, Transmissible Encephalopathy of mink, Chronic Wasting Disease of cervids, and Bovine Spongiform Encephalopathy of cattle. In human, it causes Creutzfeldt-Jakob disease (CJD), of which Kuru is another known variant. Stanley B. Prusiner in the year 1982 first coined the term \u201cPrion\u201d while explaining the cause of Scrapie in sheep. Prusiner published this study in the scientific journal \u201cScience\u201d under the title \u201cNovel Proteinaceous Infectious Particles Cause Scrapie\u201d. One of the lines mentioned in the land mark paper is quoted below- <\/span><\/span><\/p>\n<p style=\"text-align: justify;\" align=\"JUSTIFY\"><span style=\"color: #000000;\">\u201c<span style=\"font-size: large;\"><i><b>Because the novel properties of the Scrapie agent distinguish it from viruses, plasmids, and viroids, a new term &#8220;prion&#8221; is proposed to denote a small proteinaceous infectious particle, which is resistant to inactivation by most procedures that modify nucleic acids.\u201d<\/b><\/i><\/span><\/span><\/p>\n<p style=\"text-align: right;\" align=\"RIGHT\"><span style=\"font-family: 'Times New Roman', serif; color: #000000;\"><span style=\"font-size: large;\">-Stanley B. Prusiner<\/span><\/span><\/p>\n<p style=\"text-align: justify;\" align=\"JUSTIFY\"><span style=\"color: #000000;\"><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">The prion proteins (PrP) are found throughout the body of healthy human and animals. The PrP found in infectious material has a structural&nbsp;difference&nbsp;with the normal PrP and they are resistant to protease. The normal form of the Prion protein is called&nbsp;PrP<\/span><\/span><sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">C<\/span><\/span><\/sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">, while the infectious form is known as&nbsp;PrP<\/span><\/span><sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">Sc<\/span><\/span><\/sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">, where the&nbsp;C&nbsp;refers to &#8216;cellular&#8217; PrP and the&nbsp;Sc&nbsp;refers to &#8216;Scrapie&#8217;. The structure of Normal cellular prion protein (PrP<\/span><\/span><sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">C<\/span><\/span><\/sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">) is well-defined while the same for&nbsp;PrP<\/span><\/span><sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">Sc<\/span><\/span><\/sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">&nbsp;is polydisperse and defined at a relatively poor level (Wikipedia).<\/span><\/span><\/span><\/p>\n<p style=\"text-align: justify;\" align=\"JUSTIFY\"><span style=\"color: #000000;\"><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">Prusiner\u2019s work on Prion started with his studies on neurodegenerative diseases including Scrapie since 1972. His findings on Scrapie were against the views of majority in the scientific community at that time, who believed that Scrapie was a slow viral disease caused by some unidentified virus. Prusiner, in his Nobel Biography stated that convincing the contemporary virologists, regarding the proteinaceous nature of the infectious particle was one of the toughest jobs. In the initial years of his research on Scrapie, Prusiner\u2019s lab had hard time in arranging funding for the ongoing activities and some of the existing fundings were also discontinued for not being able to produce convincing results. He had to run after alternate financial support to keep the research going. Finally, the persistent effort of almost three decades had its most coveted climax in the Nobel Award Ceremony in the Concert Hall in Stockholm on 10<\/span><\/span><sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">th<\/span><\/span><\/sup><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\"> December 1997, where he was presented with the Nobel Prize in the field of Physiology and Medicine.<\/span><\/span><\/span><\/p>\n<p style=\"text-align: justify;\" align=\"JUSTIFY\"><span style=\"font-family: 'Times New Roman', serif; color: #000000;\"><span style=\"font-size: large;\"><b>References:<\/b><\/span><\/span><\/p>\n<ol style=\"text-align: justify;\">\n<li>\n<p align=\"JUSTIFY\"><span style=\"font-family: 'Times New Roman', serif; color: #000000;\"><span style=\"font-size: large;\">Wikipedia (<span style=\"color: #0000ff;\"><a style=\"color: #0000ff;\" href=\"#Prion_protein\">https:\/\/en.wikipedia.org\/wiki\/Prion#Prion_protein<\/a><\/span>) visited on 21-09-2017<\/span><\/span><\/p>\n<\/li>\n<li>\n<p align=\"JUSTIFY\"><span style=\"color: #000000;\"><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">Prusiner, S. B. (1982) Novel Proteinaceous Infectious Particles Cause Scrapie. <\/span><\/span><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\"><i>Science<\/i><\/span><\/span><span style=\"font-family: 'Times New Roman', serif;\"><span style=\"font-size: large;\">. 216:136-144.<\/span><\/span><\/span><\/p>\n<\/li>\n<\/ol>\n<p style=\"text-align: justify;\" align=\"CENTER\"><span style=\"color: #000000;\">&nbsp;<\/span><\/p>\n<p style=\"text-align: justify;\" align=\"CENTER\"><span style=\"color: #000000;\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-850 size-full\" src=\"https:\/\/babrone.avfu.ac.in\/blog\/wp-content\/uploads\/2017\/09\/luit.png\" alt=\"luit\" width=\"1246\" height=\"625\" srcset=\"https:\/\/babrone.avfu.ac.in\/blog\/wp-content\/uploads\/2017\/09\/luit.png 1246w, https:\/\/babrone.avfu.ac.in\/blog\/wp-content\/uploads\/2017\/09\/luit-300x150.png 300w, https:\/\/babrone.avfu.ac.in\/blog\/wp-content\/uploads\/2017\/09\/luit-768x385.png 768w, https:\/\/babrone.avfu.ac.in\/blog\/wp-content\/uploads\/2017\/09\/luit-1024x514.png 1024w, https:\/\/babrone.avfu.ac.in\/blog\/wp-content\/uploads\/2017\/09\/luit-179x90.png 179w\" sizes=\"auto, (max-width: 1246px) 100vw, 1246px\" \/><\/span><\/p>\n<p style=\"text-align: center;\" align=\"CENTER\"><span style=\"font-family: 'Times New Roman', serif; color: #000000;\"><span style=\"font-size: large;\"><b>Fig: The original paper published by Prusiner in Science<\/b><\/span><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Proteinaceous Infectious Particle, commonly abbreviated as \u2018prion\u2019, is now known as the cause of a number of diseases in animals and human. The examples of such animal diseases include Scrapie in sheep, Transmissible Encephalopathy of mink, Chronic Wasting Disease of cervids, and Bovine Spongiform Encephalopathy of cattle. In human, it causes Creutzfeldt-Jakob disease (CJD), of&#8230;<\/p>\n","protected":false},"author":1,"featured_media":851,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"ngg_post_thumbnail":0,"footnotes":""},"categories":[67,153],"tags":[87],"class_list":["post-848","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-vignette","category-vignettefourth-issue","tag-prion"],"_links":{"self":[{"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=\/wp\/v2\/posts\/848","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=848"}],"version-history":[{"count":3,"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=\/wp\/v2\/posts\/848\/revisions"}],"predecessor-version":[{"id":854,"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=\/wp\/v2\/posts\/848\/revisions\/854"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=\/wp\/v2\/media\/851"}],"wp:attachment":[{"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=848"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=848"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/babrone.avfu.ac.in\/blog\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=848"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}