Protofibril Assemblies of the Arctic, Dutch, and Flemish Mutants of the Alzheimer's Aβ1–40 Peptide

Using a coarse-grained model of the Abeta peptide, we analyze the Arctic (E22G), Dutch (E22Q), and Flemish (A21G) familial Alzheimer's disease (FAD) mutants for any changes in the stability of amyloid assemblies with respect to the wild-type (WT) sequence. Based on a structural reference state of two protofilaments aligned to create the "agitated" protofibril as determined by solid-state NMR, we determine free energy trends for Abeta assemblies for the WT and FAD familial sequences. We find that the structural characteristics and oligomer size of the critical nucleus vary dramatically among th... Mehr ...

Verfasser: Fawzi, Nicolas Lux
Kohlstedt, Kevin L
Okabe, Yuka
Head-Gordon, Teresa
Dokumenttyp: Artikel
Erscheinungsdatum: 2008
Reihe/Periodikum: Biophysical Journal, vol 94, iss 6
Verlag/Hrsg.: eScholarship
University of California
Schlagwörter: Biochemistry and Cell Biology / Biological Sciences / Neurosciences / Aging / Neurodegenerative / Alzheimer's Disease / Acquired Cognitive Impairment / Dementia / Brain Disorders / Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) / Alzheimer Disease / Amyloid beta-Peptides / Arctic Regions / Chromatography / Genetic Predisposition to Disease / Magnetic Resonance Spectroscopy / Models / Statistical / Molecular Conformation / Mutation / Netherlands / Peptide Fragments / Peptides / Protein Conformation / Protein Structure / Secondary / Proteins / Thermodynamics / Physical Sciences / Chemical Sciences / Biophysics
Sprache: unknown
Permalink: https://search.fid-benelux.de/Record/base-26791922
Datenquelle: BASE; Originalkatalog
Powered By: BASE
Link(s) : https://escholarship.org/uc/item/8qw2m08v