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- W3015182592 endingPage "115487" @default.
- W3015182592 startingPage "115487" @default.
- W3015182592 abstract "The incorporation of nucleotides equipped with C-glycosidic aromatic nucleobases into DNA and RNA is an alluring strategy for a number of practical applications including fluorescent labelling of oligonucleotides, expansion of the genetic alphabet for the generation of aptamers and semi-synthetic organisms, or the modulation of excess electron transfer within DNA. However, the generation of C-nucleoside containing oligonucleotides relies mainly on solid-phase synthesis which is quite labor intensive and restricted to short sequences. Here, we explore the possibility of constructing biphenyl-modified DNA sequences using enzymatic synthesis. The presence of multiple biphenyl-units or biphenyl residues modified with electron donors and acceptors permits the incorporation of a single dBphMP nucleotide. Moreover, templates with multiple abasic sites enable the incorporation of up to two dBphMP nucleotides, while TdT-mediated tailing reactions produce single-stranded DNA oligonucleotides with four biphenyl residues appended at the 3′-end." @default.
- W3015182592 created "2020-04-10" @default.
- W3015182592 creator A5037610272 @default.
- W3015182592 creator A5038016298 @default.
- W3015182592 creator A5052169343 @default.
- W3015182592 creator A5069127423 @default.
- W3015182592 date "2020-06-01" @default.
- W3015182592 modified "2023-10-17" @default.
- W3015182592 title "Enzymatic synthesis of biphenyl-DNA oligonucleotides" @default.
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- W3015182592 doi "https://doi.org/10.1016/j.bmc.2020.115487" @default.
- W3015182592 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/32284226" @default.
- W3015182592 hasPublicationYear "2020" @default.
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