Journal
CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 13, Pages 5009-5022Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201406392
Keywords
HNA; isoG; polymerase; nucleosides; XNA plasmid
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Funding
- European Research Council under the European Union [ERC-2012-ADG_20120216/320683]
- MRC [MC_U105178804] Funding Source: UKRI
- Medical Research Council [MC_U105178804] Funding Source: researchfish
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The synthesis, base-pairing properties and in vitro and in vivo characteristics of 5-methyl-isocytosine (isoC(Me)) and isoguanine (isoG) nucleosides, incorporated in an HNA(h) (hexitol nucleic acid)-DNA(d) mosaic backbone, are described. The required h-isoG phosphoramidite was prepared by a selective deamination as a key step. As demonstrated by T-m measurements the hexitol sugar showed slightly better mismatch discrimination against dT. The d-isoG base mispairing follows the order T> G> C while the h-isoG base mispairing follows the order G> C> T. The h-and d-isoCMe bases mainly mispair with G. Enzymatic incorporation experiments show that the hexitol backbone has a variable effect on selectivity. In the enzymatic assays, isoG misincorporates mainly with T, and isoC(Me) misincorporates mainly with A. Further analysis in vivo confirmed the patterns of base-pair interpretation for the deoxyribose and hexitol isoC(Me)/isoG bases in a cellular context, through incorporation of the bases into plasmidic DNA. Results in vivo demonstrated that mispairing and misincorporation was dependent on the backbone scaffold of the base, which indicates rational advances towards orthogonality.
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