Interaction study of arsenic (III and V) ions with metallothionein gene (MT2A) fragment
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25218889
DOI
10.1016/j.ijbiomac.2014.09.001
PII: S0141-8130(14)00597-2
Knihovny.cz E-zdroje
- Klíčová slova
- Anticancer drug, Arsenic, DNA Interaction, Electrochemistry, Spectrometry,
- MeSH
- antitumorózní látky chemie terapeutické užití MeSH
- arsen škodlivé účinky terapeutické užití MeSH
- DNA chemie účinky léků genetika MeSH
- fragmentace DNA účinky léků MeSH
- infekční nemoci farmakoterapie patologie MeSH
- ionty chemie MeSH
- lidé MeSH
- metalothionein chemie genetika MeSH
- spektrofotometrie atomová MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antitumorózní látky MeSH
- arsen MeSH
- DNA MeSH
- ionty MeSH
- metalothionein MeSH
- MT2A protein, human MeSH Prohlížeč
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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