Analysis of T-rich oligonucleotides labelled with osmium tetroxide 2,2´- bipyridine by capillary zone electrophoresis

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F10%3A00043430" target="_blank" >RIV/00216224:14310/10:00043430 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Analysis of T-rich oligonucleotides labelled with osmium tetroxide 2,2´- bipyridine by capillary zone electrophoresis

Popis výsledku v původním jazyce

Labeling of nucleic acids offers broader option for its biochemical and physicochemical studies by the analytical separation methods such as capillary electrophoresis. Suitable labeling allows monitoring of DNA hybridization as well as following of DNA interactions with other biological and/or non-biological compounds. Chemical DNA probe consisting of osmium tetroxide and 2,2'-bipyridine (Os,bipy) is well-known especially for its electrochemical activity. In contrary to vanishing reactivity with purines, Os,bipy reagent creates covalent adducts with pyrimidine bases. The fastest adduct formation was observed namely with thymine. In our work, we analyzed selected pentanucleotides with various number and position of thymine bases and we monitored its reactivity with Os,bipy reagent. Our interest was also taken to ageing of Os,bipy reagent and the role of reagent abundance in mixture with oligonucleotide was studied.

Název v anglickém jazyce

Analysis of T-rich oligonucleotides labelled with osmium tetroxide 2,2´- bipyridine by capillary zone electrophoresis

Popis výsledku anglicky

Labeling of nucleic acids offers broader option for its biochemical and physicochemical studies by the analytical separation methods such as capillary electrophoresis. Suitable labeling allows monitoring of DNA hybridization as well as following of DNA interactions with other biological and/or non-biological compounds. Chemical DNA probe consisting of osmium tetroxide and 2,2'-bipyridine (Os,bipy) is well-known especially for its electrochemical activity. In contrary to vanishing reactivity with purines, Os,bipy reagent creates covalent adducts with pyrimidine bases. The fastest adduct formation was observed namely with thymine. In our work, we analyzed selected pentanucleotides with various number and position of thymine bases and we monitored its reactivity with Os,bipy reagent. Our interest was also taken to ageing of Os,bipy reagent and the role of reagent abundance in mixture with oligonucleotide was studied.

Druh

D - Stať ve sborníku

CEP obor

CB - Analytická chemie, separace

OECD FORD obor

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Projekt

<a href="/cs/project/LC06035" target="_blank" >LC06035: Centrum biofyzikální chemie, bioelektrochemie a bioanalýzy. Nové nástroje pro genomiku, proteomiku a biomedicínu.</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Rok uplatnění

2010

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název statě ve sborníku

Acta Universitatis Palackianae Olomucensis Chemica 47S

ISBN

978-80-244-2470-5

ISSN

0232-0061

e-ISSN

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Počet stran výsledku

158

Strana od-do

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Název nakladatele

Palacký University, Olomouc

Místo vydání

Olomouc

Místo konání akce

Olomouc, Czech Republic

Datum konání akce

8. 2. 2010

Typ akce podle státní příslušnosti

EUR - Evropská akce

Kód UT WoS článku

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