Aluminum, copper, iron and zinc differentially alter amyloid-Aβ 1-42 aggregation and toxicity

International Journal of Biochemistry and Cell Biology

Volumn 43, Issue 6, 2011, Pages 877-885

  Bolognin, Silvia ^a   Messori, Luigi ^b   Drago, Denise ^c   Gabbiani, Chiara ^b   Cendron, Laura ^d   Zatta, Paolo ^d  

^a NEW YORK STATE INSTITUTE FOR BASIC RESEARCH IN DEVELOPMENTAL DISABILITIES   (United States)

^b UNIVERSITY OF FLORENCE   (Italy)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF PADOVA   (Italy)

Author keywords

Alzheimer's disease; Amyloid precursor protein; Metal ions; Oligomers; Tau

Indexed keywords

ALUMINUM; AMYLOID BETA PROTEIN[1-42]; COPPER; IRON; METAL COMPLEX; ZINC;

ARTICLE; COMPLEX FORMATION; DOT HYBRIDIZATION; ELECTROSPRAY MASS SPECTROMETRY; FLUORESCENCE ANALYSIS; HUMAN; HUMAN CELL; LIGHT SCATTERING; METAL BINDING; NEUROBLASTOMA CELL; NEUROTOXICITY; PROTEIN AGGREGATION; TRANSMISSION ELECTRON MICROSCOPY;

ALUMINUM; ALZHEIMER DISEASE; AMYLOID; AMYLOID BETA-PEPTIDES; CELL LINE, TUMOR; COPPER; HUMANS; IRON; MASS SPECTROMETRY; MICROSCOPY, ELECTRON, TRANSMISSION; NEURONS; NEUROTOXICITY SYNDROMES; PEPTIDE FRAGMENTS; PROTEIN MULTIMERIZATION; ZINC;

EID: 79955927181     PISSN: 13572725     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biocel.2011.02.009     Document Type: Article

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