Publication | Open Access
Fluoride‐Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer Extension
31
Citations
35
References
2011
Year
Combinatorial ChemistryBioorganic ChemistryEngineeringMolecular BiologyFull CharacterisationOrganic ChemistryChemistryChemical BiologyPrimer ExtensionDna NanotechnologyFluoride TreatmentDna PolymeraseDna ComputingDna SequencingBiochemistryOligonucleotideDna ReplicationFluorous SynthesisNatural SciencesSynthetic BiologyGenome EditingReversible Terminators
Fluorescent 2'-deoxynucleotides containing a protecting group at the 3'-O-position are reversible terminators that enable array-based DNA sequencing-by-synthesis (SBS) approaches. Herein, we describe the synthesis and full characterisation of four reversible terminators bearing a 3'-blocking moiety and a linker-dye system that is removable under the same fluoride-based treatment. Each nucleotide analogue has a different fluorophore attached to the base through a fluoride-cleavable linker and a 2-cyanoethyl moiety as the 3'-blocking group, which can be removed by using a fluoride treatment as well. Furthermore, we identified a DNA polymerase, namely, RevertAid M-MuLV reverse transcriptase, which can incorporate the four modified reversible terminators. The synthesised nucleotides and the optimised DNA polymerase were used on CodeLink slides spotted with hairpin oligonucleotides to demonstrate their potential in a cyclic reversible terminating approach.
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