Detailed Information on Publication Record
2012
Electrochemical detection of 5-methylcytosine in bisulfite-treated DNA
BARTOSIK, Martin, Miroslav FOJTA and Emil PALECEKBasic information
Original name
Electrochemical detection of 5-methylcytosine in bisulfite-treated DNA
Authors
BARTOSIK, Martin (203 Czech Republic), Miroslav FOJTA (203 Czech Republic, guarantor, belonging to the institution) and Emil PALECEK (203 Czech Republic)
Edition
Electrochimica Acta, Oxford, Pergamon-Elsevier Science, 2012, 0013-4686
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10610 Biophysics
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
Impact factor
Impact factor: 3.777
RIV identification code
RIV/00216224:14740/12:00073027
Organization unit
Central European Institute of Technology
UT WoS
000308259500010
Keywords in English
DNA methylation; 5-Methylcytosine analysis; Sodium bisulfite; Mercury electrode; Solid amalgam electrode
Tags
International impact, Reviewed
Změněno: 13/4/2014 10:30, Olga Křížová
Abstract
V originále
DNA methylation is an important epigenetic event playing crucial roles in physiologic and pathologic processes. We show that methylation of cytosine (C) residues in DNA can be easily detected electrochemically using mercury or solid amalgam electrodes. Reduction peaks of untreated single-stranded methylated and non-methylated oligodeoxynucleotides (ODN) do not significantly differ. Using DNA bisulfite treatment, reducible Cs are transformed into nonreducible uracil residues, strongly decreasing square wave voltammetric C reduction peaks. On the other hand. 5-methylcytosine (mC) residues resist the bisulfite treatment and display almost unchanged reduction peak. Desulfonation step should be omitted because uracil sulfonation improves the resolution of C from mC. By combining DNA bisulfite treatment with square wave voltammetry. DNA methylation can be determined quantitatively at nanomolar and subnamolar ODN concentrations.