2016
Interactions of fluorescent dye SYBR Green I with natural and 7-deazaguanine-modified DNA studied by fluorescence and electrochemical methods
DUDOVÁ, Zdenka; Jan ŠPAČEK; Luděk HAVRAN; Hana PIVOŇKOVÁ; Miroslav FOJTA et al.Základní údaje
Originální název
Interactions of fluorescent dye SYBR Green I with natural and 7-deazaguanine-modified DNA studied by fluorescence and electrochemical methods
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Vydání
Monatshefte fur Chemie, Wien, Springer Wien, 2016, 0026-9247
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10403 Physical chemistry
Stát vydavatele
Rakousko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 1.282
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14740/16:00090268
Organizační jednotka
Středoevropský technologický institut
UT WoS
EID Scopus
Klíčová slova anglicky
DNA; 7-Deazaguanine; PCR; Fluorescence; Quenching; DNA interaction; DNA modification; Electrochemical oxidation; Graphite electrode
Štítky
Změněno: 17. 3. 2017 15:22, Mgr. Eva Špillingová
Anotace
V originále
SYBR Green I (SG) is a fluorescent dye applied in various techniques of DNA analysis, including fluorescent staining of electrophoretic gels, quantitative polymerase chain reaction, etc. SG binds selectively to double-stranded DNA via intercalation and minor groove interactions, resulting in a considerable enhancement of fluorescence of the dye. Modification of DNA by partial or full replacement of natural purine nucleobase guanine (G) with its synthetic analog 7-deazaguanine (G*) or its derivatives was shown to cause the SG fluorescence quenching. In this paper, we present a comparative study of interactions of SG with natural DNA fragments and with DNA fragments modified with G* by means of fluorescence and electrochemical methods. Competition between unmodified (forming strongly fluorescent complex with SG) and fully G*-modified (not contributing significantly to overall fluorescence signal) DNA fragments for the dye was studied via changes in the fluorescence intensity. In addition, association interactions of natural or G*-modified DNA with SG in solution were monitored by adsorptive transfer stripping square wave voltammetry at a pyrolytic graphite electrode using a signal of SG electrooxidation. We show that SG binds both natural and G*-modified DNA with similar apparent affinity and selectivity for the double-stranded DNA. [GRAPHICS] .