Illustration of Prion Infection Mechanism

FIGURE 20–21 Prion Infection Mechanism Prions are misfolded PrP proteins. The build-up of prions in brain tissue can cause disease by damaging nerve cells.

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Prions In 1972, American scientist Stanley Prusiner became interested in scrapie, an infectious disease in sheep, the exact cause of which was unknown. At first, he suspected a viral cause, but experiments revealed clumps of tiny protein particles in the brains of infected sheep. Prusiner called these particles prions, short for “protein infectious particles.” Although prions were first discovered in sheep, many animals, including humans, can become infected with prions. Prions are formed when a protein known as PrP is improperly folded. Prions themselves can cause PrP proteins to misfold, producing even more prions. An accumulation of prions can damage nerve cells, as shown in Figure 20–21.


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Table of Contents

Miller & Levine Biology UNIT 1 The Nature of Life UNIT 2 Ecology UNIT 3 Cells UNIT 4 Genetics UNIT 5 Evolution UNIT 6 From Microorganisms to Plants UNIT 7 Animals UNIT 8 The Human Body A Visual Guide to The Diversity of Life Appendices Glossary Index Credits