Interaction study of arsenic (III and V) ions with metallothionein gene (MT2A) fragment
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25218889
DOI
10.1016/j.ijbiomac.2014.09.001
PII: S0141-8130(14)00597-2
Knihovny.cz E-resources
- Keywords
- Anticancer drug, Arsenic, DNA Interaction, Electrochemistry, Spectrometry,
- MeSH
- Arsenic adverse effects therapeutic use MeSH
- DNA chemistry drug effects genetics MeSH
- DNA Fragmentation drug effects MeSH
- Communicable Diseases drug therapy pathology MeSH
- Ions chemistry MeSH
- Humans MeSH
- Metallothionein chemistry genetics MeSH
- Antineoplastic Agents chemistry therapeutic use MeSH
- Spectrophotometry, Atomic MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Arsenic MeSH
- DNA MeSH
- Ions MeSH
- Metallothionein MeSH
- MT2A protein, human MeSH Browser
- Antineoplastic Agents MeSH
Arsenic compounds belong to the most controversial agents concerning human health. Arsenic (As) is considered as a top environmental element influencing human health due to its adverse effects including cancer, diabetes, cardiovascular disease, and reproductive or developmental problems. Despite the proven mutagenic, teratogenic and carcinogenic effects, the arsenic compounds are used for centuries to treat infectious diseases. In our work, we focused on studying of interactions of As(III) and/or As(V) with DNA. Interactions between arsenic ions and DNA were monitored by UV/vis spectrophotometry by measuring absorption and fluorescence spectra, atomic absorption spectrometry, electrochemical measurements (square wave voltammetry) and agarose gel electrophoresis. Using these methods, we observed a stable structure of DNA with As(III) within the concentration range 0.4-6.25 μg mL(-1). Higher As(III) concentration caused degradation of DNA. However, similar effects were not observed for As(V).
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