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Copper(II) coordination to amyloid β: murine versus human peptide

Hélène Eury1, Christian Bijani, Peter Faller

  • 1CNRS, Laboratoire de Chimie de Coordination, 205, route de Narbonne, 31077 Toulouse, France.

Angewandte Chemie (International Ed. in English)
|January 20, 2011
PubMed
Abstract

No abstract available in PubMed .

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Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
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