Repozytorium

Biological inorganic and bioinorganic chemistry of neurodegeneration based on prion and Alzheimer diseases.

Autorzy

David R. Brown

Henryk Kozłowski

Rok wydania

2004

Czasopismo

Dalton Transactions

Strony

1907-1917

DOI

10.1039/b401985g

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

A change of the prion protein conformation results in a class of neurodegenerative diseases called the transmissible spongiform encephalopathies (like mad cow and Creutzfeld-Jakob diseases). The function of the normal prion protein is unknown, although much of recent research demonstrates the it may be a copper binding protein selective for Cu(II). Amyloid precursor protein (APP) releases the 39-42 amino acid peptide, a major constituent of the deposit in plaques of Alzheimer disease brain. Also APP is a metal binding protein, including copper ions. The link between copper and both proteins may provide insight into the role of metals in neurodegenerative pathologies.

Adres publiczny

https://doi.org/10.1039/b401985g

Strona internetowa wydawcy

https://www.rsc.org/

Podobne publikacje
2007

Impact of copper ions on chemistry and biology of prion protein.

Janicka Anna, Stańczak Paweł, Kozłowski Henryk