A label-free electrochemical test for DNA-binding activities of tumor suppressor protein p53 using immunoprecipitation at magnetic beads
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
20493293
DOI
10.1016/j.aca.2010.04.018
PII: S0003-2670(10)00420-4
Knihovny.cz E-zdroje
- MeSH
- biosenzitivní techniky * metody MeSH
- DNA metabolismus MeSH
- elektrochemické techniky * metody MeSH
- elektrody MeSH
- elektroforéza v agarovém gelu MeSH
- imunoprecipitace * metody MeSH
- kompetitivní vazba MeSH
- lidé MeSH
- magnetismus MeSH
- myši MeSH
- nádorový supresorový protein p53 * analýza genetika metabolismus MeSH
- rtuť MeSH
- vazebná místa MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- DNA MeSH
- nádorový supresorový protein p53 * MeSH
- rtuť MeSH
In this paper we extend the application area of the label-free structure-sensitive electrochemical DNA sensing with mercury-based electrodes which is for the first time used, in combination with immunoprecipitation at magnetic beads (MB), for the probing of DNA interactions with tumor suppressor protein p53. The technique relies on capture of the p53-DNA complexes at MB via anti-p53 antibodies, followed by salt-induced dissociation of linear DNA from the complex and its voltammetric detection. Competitive binding of p53 to various plasmid DNA substrates, including lin or scDNAs with or without a specific target site, can easily be followed by ex situ electrochemical analysis of DNA recovered from the immunoprecipitated complexes. Compared to gel electrophoresis which is usually applied to analyze different plasmid DNA forms and their complexes with proteins, the electrochemical detection is faster and allows simpler quantitation of DNA containing free ends at submicrogram levels. We demonstrate applicability of the proposed technique to monitor different DNA-binding activities of wild type and mutant p53 proteins.
Citace poskytuje Crossref.org
Preferential binding of hot spot mutant p53 proteins to supercoiled DNA in vitro and in cells