The oxidation double peak of reduced guanine residues in short oligodeoxynucleotides: A study of its origin
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F18%3A00106524" target="_blank" >RIV/00216224:14310/18:00106524 - isvavai.cz</a>
Výsledek na webu
<a href="https://doi.org/10.1016/j.jelechem.2018.03.013" target="_blank" >https://doi.org/10.1016/j.jelechem.2018.03.013</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.jelechem.2018.03.013" target="_blank" >10.1016/j.jelechem.2018.03.013</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
The oxidation double peak of reduced guanine residues in short oligodeoxynucleotides: A study of its origin
Popis výsledku v původním jazyce
The aim of this study is to find a deeper understanding of the long neglected oxidation double peak of reduced guanines (G(red)ODP) produced at a mercury electrode (ME) by the reverse oxidation of the guanine reduction product (G(red)). Although the reduction processes of G moieties at an ME are hidden in the cathodic currents of the background solvent decompositions, and the G reduction process thus cannot be examined directly, the G reduction product can be oxidized back to G, yielding an oxidation signal at about 0.2V. depending on the measurement conditions, the oxidation signal of Gred may assume the form of a single peak or a double peak with GI and GII. The cause of the double peak generation remains unknown. However, the novel approach based on combining elements of chronoamperometry and voltammetry proposes that the G(red)ODP originates from the oxidation of DNA fragments in two different adsorption conformations. The results indicate thet the orientation of G residues is controlled by the repulsive interaction after thier reduction and from the difference of GI and GII potentials the repulsion energy was estimated. The new findings may find application as a tool to indicate the structural and surface properties of short oligonucleotides with G bases
Název v anglickém jazyce
The oxidation double peak of reduced guanine residues in short oligodeoxynucleotides: A study of its origin
Popis výsledku anglicky
The aim of this study is to find a deeper understanding of the long neglected oxidation double peak of reduced guanines (G(red)ODP) produced at a mercury electrode (ME) by the reverse oxidation of the guanine reduction product (G(red)). Although the reduction processes of G moieties at an ME are hidden in the cathodic currents of the background solvent decompositions, and the G reduction process thus cannot be examined directly, the G reduction product can be oxidized back to G, yielding an oxidation signal at about 0.2V. depending on the measurement conditions, the oxidation signal of Gred may assume the form of a single peak or a double peak with GI and GII. The cause of the double peak generation remains unknown. However, the novel approach based on combining elements of chronoamperometry and voltammetry proposes that the G(red)ODP originates from the oxidation of DNA fragments in two different adsorption conformations. The results indicate thet the orientation of G residues is controlled by the repulsive interaction after thier reduction and from the difference of GI and GII potentials the repulsion energy was estimated. The new findings may find application as a tool to indicate the structural and surface properties of short oligonucleotides with G bases
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)
Návaznosti výsledku
Projekt
<a href="/cs/project/LD15058" target="_blank" >LD15058: Příprava substrátů pro povrchově zesílenou Ramanovu spektroskopii pomocí elektrochemických, elektroforetických a jiskrový výboj využívajících technik.</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach
Ostatní
Rok uplatnění
2018
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Electroanalytical Chemistry
ISSN
1572-6657
e-ISSN
1873-2569
Svazek periodika
821
Číslo periodika v rámci svazku
July
Stát vydavatele periodika
CZ - Česká republika
Počet stran výsledku
7
Strana od-do
104-110
Kód UT WoS článku
000437818600017
EID výsledku v databázi Scopus
2-s2.0-85046100800