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The α and β domains of human metallothionein-3 co-operatively protect against Aβ 1-42-Cu 2+ cytotoxicity

  • Ying Luo
  • , Yu Xia Xu
  • , Qin Gui Bao
  • , Zhi-Chun Ding
  • , Cui Qing Zhu
  • , Zhong Xian Huang
  • , Xiang Shi Tan

Research output: Contribution to journalArticlepeer-review

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 languageEnglish (US)
Pages (from-to)1193-1196
Number of pages4
JournalChinese Chemical Letters
Volume23
Issue number10
DOIs
StatePublished - Oct 2012
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Alzheimer's disease
  • ROS
  • Toxicity
  • Zn MT3

ASJC Scopus subject areas

  • General Chemistry

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