Stanley B. Prusiner

Prusiner was born into a Jewish^[7] family in Des Moines, Iowa, the son of Miriam (Spigel) and Lawrence Prusiner, an architect. He spent his childhood in Des Moines and Cincinnati, Ohio, where he attended Walnut Hills High School, where he was known as "the little genius" for his groundbreaking work on a repellent for Boxelder bugs. Prusiner received a Bachelor of Arts degree in chemistry from the University of Pennsylvania and later received his M.D. from the University of Pennsylvania School of Medicine.^[1] Prusiner then completed an internship in medicine at the University of California, San Francisco. Later Prusiner moved to the National Institutes of Health, where he studied glutaminases in E. coli in the laboratory of Earl Stadtman.^[8]

After three years at NIH, Prusiner returned to UCSF to complete a residency in neurology. Upon completion of the residency in 1974, Prusiner joined the faculty of the UCSF Department of Neurology. Since that time, Prusiner has held various faculty and visiting faculty positions at both UCSF and UC Berkeley.^[8][9]

In 1999, Prusiner founded the IND at UCSF. The IND conducts research on neurodegenerative diseases that are caused by the accumulation of misfolded proteins. These include Creutzfeldt–Jakob disease, Alzheimer's disease, synucleinopathies and tauopathies.^[10]

In his 1998 PNAS review article on prions, Prusiner wrote^[11] "The idea that scrapie prions were composed of an amyloidogenic protein was truly heretical when it was introduced" by Tikvah Alper^[12][13]. Transmissible spongiform encephalopathies, such as scrapie and bovine spongiform encephalopathy ("mad cow disease"), are diseases that leave the brains of their victims full of holes. Scientists did not know what pathogen or disease-causing organism produced such a pattern. Prusiner and his co-workers suggested "one scientific theory, viewed as heretical in that it seems to challenge the role of nucleic acids as the exclusive carriers of genetic information." This theory suggested that the pathogen causing prion diseases might be a "deadly variety of a normal protein that has the ability to amplify itself in the brain. The hypothetical protein is called a prion (pronounced PREE-on),"^[11][14][15] a portmanteau based on the words "proteinaceous" and "infectious".^[5]

Stanley Prusiner was awarded the Nobel Prize in Physiology or Medicine in 1997 for his work in proposing an explanation for the cause of scrapie, bovine spongiform encephalopathy and human prion diseases such as Creutzfeldt–Jakob disease.^[1] He was elected to the National Academy of Sciences in 1992 and to its governing council in 2007.^[16] He is also an elected member of the American Academy of Arts and Sciences (1993),^[17] a Foreign Member of the Royal Society (ForMemRS) in 1997,^[3][18] and a member of the American Philosophical Society (1998)^[19] and the National Academy of Medicine (1992).

• Frank Bastian
• Daniel Carleton Gajdusek
• Laura Manuelidis
• List of Jewish Nobel laureates