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Merck
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  • Mass spectral studies reveal the structure of Aβ1-16-Cu2+ complex resembling ATCUN motif.

Mass spectral studies reveal the structure of Aβ1-16-Cu2+ complex resembling ATCUN motif.

Inorganic chemistry (2012-07-19)
Yamini P Ginotra, Shefali N Ramteke, Rapole Srikanth, Prasad P Kulkarni
摘要

In Alzheimer's disease, copper binds to amyloid beta (Aβ) peptide and generates oxidative stress. The coordination of histidine (His) residues to Cu(2+) is still uncertain. We studied Cu(2+) binding to Aβ1-16 peptide using the diethyl pyrocarbonate (DEPC) assay and mass spectrometry. Our results show that only one His is involved in Cu(2+) coordination, which is identified as His6 using mass spectral studies. Novel nickel displacement studies have further supported the proposal that the Cu(2+) binding site of Aβ1-16 peptide resembles the ATCUN motif of human serum albumin.

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Sigma-Aldrich
焦碳酸二乙酯, 96% (NT)
Sigma-Aldrich
焦碳酸二乙酯, 96% (NT)
Sigma-Aldrich
焦碳酸二乙酯, 96% (NT)