Abstract
Cytotoxicity of Aβ with redox active metals in neuronal cells has been implicated in the progression of Alzheimer's disease (AD). Zn 7MT-3 protects cell against Aβ-Cu 2+ toxicity. The roles of single domain proteins (α/β) and α-β domain-domain interaction of Zn 7MT-3 in its anti-Aβ 1-42-Cu 2+ toxicity activity were investigated herein. Aβ 1-42 and four mutants of human MT3 (α/β domain, β (MT3)-α (MT1) and Δ31-34) were prepared and characterized. Aβ 1-42-Cu 2+ induced hydroxyl radical and ROS production with/without Zn-MTs were measured by fluorescence spectroscopy and DCFH-DA in living cells, respectively. These results indicate that the two domains form a co-operative unit and each of them is indispensable in conducting its bioactivity.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1193-1196 |
| Number of pages | 4 |
| Journal | Chinese Chemical Letters |
| Volume | 23 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 2012 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Alzheimer's disease
- Aβ
- ROS
- Toxicity
- Zn MT3
ASJC Scopus subject areas
- General Chemistry
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