Amyloid β-protein: Monomer structure and early aggregation states of Aβ42 and its Pro19 alloform

Journal of the American Chemical Society

Volumn 127, Issue 7, 2005, Pages 2075-2084

  Bernstein, Summer L ^a   Wyttenbach, Thomas ^a   Baumketner, Andrij ^a,d   Shea, Joan Emma ^a   Bitan, Gal ^b,c   Teplow, David B ^b,c   Bowers, Michael T ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d INSTITUTE FOR CONDENSED MATTER PHYSICS   (Ukraine)

Author keywords

[No Author keywords available]

Indexed keywords

AGGLOMERATION; CROSSLINKING; DISEASES; OLIGOMERS; POLYPEPTIDES; PROTEINS;

ALZHEIMER DISEASE (AD); MONOMER STRUCTURE; NEUROPATHIC AGENT; NEUROTOXIC SPECIES;

MONOMERS;

AMYLOID BETA PROTEIN; AMYLOID BETA PROTEIN[1-40]; AMYLOID BETA PROTEIN[1-42]; DIMER; MONOMER; OLIGOMER; PHENYLALANINE; PROLINE;

ALZHEIMER DISEASE; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; CROSS LINKING; FILTER; FILTRATION; ION MOBILITY SPECTROMETRY; MASS SPECTROMETRY; NEUROTOXICITY; PHOTOCHEMISTRY; PROTEIN AGGREGATION; STRUCTURE ANALYSIS;

AMINO ACID SEQUENCE; AMYLOID BETA-PROTEIN; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; PEPTIDE FRAGMENTS; PROLINE; SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION; TEMPERATURE; WATER;

EID: 13944282886     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja044531p     Document Type: Article

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