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Synthesis and oligonucleotide incorporation of fluorescent cytosine analogue tC: a promising nucleic acid probe

Synthesis and oligonucleotide incorporation of fluorescent cytosine analogue tC: a promising nucleic acid probe
Synthesis and oligonucleotide incorporation of fluorescent cytosine analogue tC: a promising nucleic acid probe
The tricyclic cytosine, tC, is a fluorescent base analogue with excellent properties for investigating intrinsic characteristics of nucleic acid as well as interactions between nucleic acids and other molecules. Its unique fluorescence properties and insignificant influence on overall structure and dynamics of nucleic acid after incorporation makes tC particularly interesting in fluorescence resonance energy transfer and anisotropy measurements. We here describe a straightforward synthesis of the standard monomer form of tC for DNA solid-phase synthesis, the tC phosphoramidite, and its subsequent incorporation into oligonucleotides. The total synthesis of the tC phosphoramidite takes approximately 8 days and its incorporation and the subsequent oligonucleotide purification an additional day.
5-arylthiopyrimidines, dna-base analog, dynamics, guanosine analog, pairs, 2'-deoxycytidine, 2-aminopurine, pteridine nucleoside analogs, sequence, derivatives
1745-2473
615-623
Sandin, P.
9ee41860-1744-4633-b94a-8ac613982dbf
Lincoln, P.
754c479f-0b1e-43ba-85df-3c691fb379c8
Brown, T.
a64aae36-bb30-42df-88a2-11be394e8c89
Wilhelmsson, L.M.
ff5f2ef9-e2ec-4e29-92da-7696957da11c
Sandin, P.
9ee41860-1744-4633-b94a-8ac613982dbf
Lincoln, P.
754c479f-0b1e-43ba-85df-3c691fb379c8
Brown, T.
a64aae36-bb30-42df-88a2-11be394e8c89
Wilhelmsson, L.M.
ff5f2ef9-e2ec-4e29-92da-7696957da11c

Sandin, P., Lincoln, P., Brown, T. and Wilhelmsson, L.M. (2007) Synthesis and oligonucleotide incorporation of fluorescent cytosine analogue tC: a promising nucleic acid probe. Nature Physics, 2 (3), 615-623. (doi:10.1038/nprot.2007.80).

Record type: Article

Abstract

The tricyclic cytosine, tC, is a fluorescent base analogue with excellent properties for investigating intrinsic characteristics of nucleic acid as well as interactions between nucleic acids and other molecules. Its unique fluorescence properties and insignificant influence on overall structure and dynamics of nucleic acid after incorporation makes tC particularly interesting in fluorescence resonance energy transfer and anisotropy measurements. We here describe a straightforward synthesis of the standard monomer form of tC for DNA solid-phase synthesis, the tC phosphoramidite, and its subsequent incorporation into oligonucleotides. The total synthesis of the tC phosphoramidite takes approximately 8 days and its incorporation and the subsequent oligonucleotide purification an additional day.

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More information

Published date: 2007
Keywords: 5-arylthiopyrimidines, dna-base analog, dynamics, guanosine analog, pairs, 2'-deoxycytidine, 2-aminopurine, pteridine nucleoside analogs, sequence, derivatives

Identifiers

Local EPrints ID: 54377
URI: http://eprints.soton.ac.uk/id/eprint/54377
ISSN: 1745-2473
PURE UUID: 1a8677a7-6c25-4179-ba53-338cf65ae6c7

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Date deposited: 31 Jul 2008
Last modified: 15 Mar 2024 10:47

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Contributors

Author: P. Sandin
Author: P. Lincoln
Author: T. Brown
Author: L.M. Wilhelmsson

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