Role of Metal Ions in the Self-assembly of the Alzheimer's Amyloid-β Peptide

被引:318
作者
Faller, Peter [1 ]
Hureau, Christelle
Berthoumieu, Olivia
机构
[1] CNRS, Chim Coordinat Lab, F-31077 Toulouse 4, France
关键词
A-BETA; IN-VITRO; PRECURSOR PROTEIN; ZINC-BINDING; PHYSIOLOGICAL CONCENTRATIONS; NEURODEGENERATIVE DISEASES; COPPER COORDINATION; INDUCED AGGREGATION; STRUCTURAL BASIS; REDOX CHEMISTRY;
D O I
10.1021/ic4003059
中图分类号
O61 [无机化学];
学科分类号
070301 [无机化学];
摘要
Aggregation of amyloid-beta (A beta) by self-assembly into oligomers or amyloids is a central event in Alzheimer's disease. Coordination of transition-metal ions, mainly copper and zinc, to A beta occurs in vivo and modulates the aggregation process. A survey of the impact of Cu-II and Zn-II on the aggregation of A beta reveals some general trends: (i) Zn-II and Cu-II at high micromolar concentrations and/or in a large superstoichiometric ratio compared to A beta have a tendency to promote amorphous aggregations (precipitation) over the ordered formation of fibrilar amyloids by self-assembly; (ii) metal ions affect the kinetics of A beta aggregations, with the most significant impact on the nucleation phase; (iii) the impact is metal-specific; (iv) Cu-II and Zn-II affect the concentrations and/or the types of aggregation intermediates formed; (v) the binding of metal ions changes both the structure and the charge of A beta. The decrease in the overall charge at physiological pH increases the overall driving force for aggregation but may favor more precipitation over fibrillation, whereas the induced structural changes seem more relevant for the amyloid formation.
引用
收藏
页码:12193 / 12206
页数:14
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