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Protected 5-(hydroxymethyl)uracil nucleotides bearing visible-light photocleavable groups as building blocks for polymerase synthesis of photocaged DNA
S. Boháčová, L. Ludvíková, L. Poštová Slavětínská, Z. Vaníková, P. Klán, M. Hocek,
Language English Country England, Great Britain
Document type Journal Article
PubMed
29431832
DOI
10.1039/c8ob00160j
Knihovny.cz E-resources
- MeSH
- DNA-Directed DNA Polymerase metabolism MeSH
- DNA biosynthesis chemistry MeSH
- Photochemical Processes * MeSH
- Nucleic Acid Conformation MeSH
- Models, Molecular MeSH
- Nucleotides chemistry MeSH
- Pentoxyl analogs & derivatives chemistry MeSH
- Light * MeSH
- Publication type
- Journal Article MeSH
Nucleosides, nucleotides and 2'-deoxyribonucleoside triphosphates (dNTPs) containing 5-(hydroxymethyl)uracil protected with photocleavable groups (2-nitrobenzyl-, 6-nitropiperonyl or 9-anthrylmethyl) were prepared and tested as building blocks for the polymerase synthesis of photocaged oligonucleotides and DNA. Photodeprotection (photorelease) reactions were studied in detail on model nucleoside monophosphates and their photoreaction quantum yields were determined. Photocaged dNTPs were then tested and used as substrates for DNA polymerases in primer extension or PCR. DNA probes containing photocaged or free 5-hydroxymethylU in the recognition sequence of restriction endonucleases were prepared and used for the study of photorelease of caged DNA by UV or visible light at different wavelengths. The nitropiperonyl-protected nucleotide was found to be a superior building block because the corresponding dNTP is a good substrate for DNA polymerases, and the protecting group is efficiently cleavable by irradiation by UV or visible light (up to 425 nm).
References provided by Crossref.org
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