Zinc(II) binds to the neuroprotective peptide humanin

被引:54
作者
Armas, Ambar
Sonois, Vanessa
Mothes, Emmanuelle
Mazarguil, Honore
Faller, Peter
机构
[1] Univ Toulouse 1, CNRS, UPR 8241, Chim Coordinat Lab, F-31077 Toulouse, France
[2] Inst Pharmacol & Biol Struct, F-31077 Toulouse, France
关键词
humanin; zinc; Alzheimer's disease; glutathione; amyloid beta;
D O I
10.1016/j.jinorgbio.2006.06.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The abnormal accumulation of the peptide amyloid-beta in the form of senile (or amyloid) plaques is one of the hallmarks of Alzheimer's disease (AD). Zinc ions have been implicated in AD and plaques formation. Recently, the peptide humanin has been discovered. Humanin showed neuroprotective activity against amyloid-beta insults. Here the question investigated is if humanin could interact directly with Zn-II. It is shown that Zn-II and its substitutes Cd-II/Co-II bind to humanin via a thiolate bond from the side chain of the single cysteine at position 8. The low intensity of the d-d bands of Con-humanin indicated an octahedral coordination geometry. Titration experiments suggest that Zn-II binds to humanin with an apparent affinity in the low M range. This apparent Zn-binding affinity is in the same order as for amyloid-beta and glutathione and could thus be of physiological relevance. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1672 / 1678
页数:7
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