Detailed Information on Publication Record
2017
Magnetic bead-based electrochemical assay for determination of DNA methyltransferase activity
DUDOVÁ, Zdenka, Martin BARTOŠÍK and Miroslav FOJTABasic information
Original name
Magnetic bead-based electrochemical assay for determination of DNA methyltransferase activity
Authors
Edition
Electrochimica Acta, Amsterdam, Elsevier Science, 2017, 0013-4686
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10405 Electrochemistry
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.116
UT WoS
000398324500066
Keywords in English
DNA methyltransferase; DNA methylation; magnetic beads; restriction endonuclease; carbon electrode
Tags
International impact, Reviewed
Změněno: 12/5/2022 21:39, Mgr. Zdenka Dudová, Ph.D.
Abstract
V originále
DNA methylation, an epigenetic mechanism playing important role in many cellular processes, is carried out via action of DNA methyltransferase (MTase) enzymes. Increasing evidence shows that altered activity of MTases may cause aberrant DNA methylation, which in turn may lead to malignant transformation, and ultimately to cancer. Assessing MTase activity is thus considered of high importance in early cancer diagnostics. Electrochemistry represents an interesting alternative to current methods of MTase analysis, as it is relatively inexpensive, fast and simple. We describe here a development of electrochemical assay in which DNA probe, containing restriction sites CCGG for HapII endonuclease and bearing biotin label at its distal end, is immobilized at magnetic beads and incubated in MTase solution. Methylation of DNA then blocks restriction by HapII and the terminal biotin moiety is preserved to be available for attachment of alkaline phosphatase producing an electroactive indicator, yielding electrochemical signal from the methylated DNA. On the other hand, without MTase the DNA is not methylated and thus the biotinylated DNA end is cleaved-off, leading to the signal diminution. The assay is simple and quick, requiring less than 3 h to completely assess MTase activity. (C) 2017 Elsevier Ltd. All rights reserved.
Links
GBP206/12/G151, research and development project |
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