Evolutionary Implications of Metal Binding Features in Different Species’ Prion Protein: An Inorganic Point of View

Prion disorders are a group of fatal neurodegenerative conditions of mammals. The key molecular event in the pathogenesis of such diseases is the conformational conversion of prion protein, PrPC, into a misfolded form rich in β-sheet structure, PrPSc, but the detailed mechanistic aspects of prion p...

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Bibliographic Details
Main Authors: Diego La Mendola, Enrico Rizzarelli
Format: Article
Language:English
Published: MDPI AG 2014-05-01
Series:Biomolecules
Subjects:
Online Access:http://www.mdpi.com/2218-273X/4/2/546