RSS-Feed abonnieren
DOI: 10.1055/a-2071-7168
Acyclic 2-Ethynylnaphthalene-Modified 8-Aza-3,7-dideaza-2′-deoxyadenosine Allows Thymine Discrimination by Probing the DNA Minor Groove Environment
This work was supported by the Japan Society for the Promotion of Science (MEXT, KAKENHI) (Grant No. 19K05700).
Abstract
Two novel acyclic environment-sensitive fluorescent nucleosides named ac37zA and an37zA are synthesized and their photophysical properties are investigated. Both ac37zA and an37zA exhibit dual fluorescence emission depending upon molecular coplanarity. Oligodeoxynucleotide probes containing ac37zA clearly discriminate perfectly matched thymine in target DNA strands by strong charge transfer (CT) emission in the longer wavelength region and by strong quenching of emission from the twisted conformation in the mismatched case.
Key words
acyclic nucleoside - DNA - single-nucleotide polymorphism (SNP) - adenine - thymine - solvatochromicitySupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2071-7168.
- Supporting Information
Publikationsverlauf
Eingereicht: 14. Februar 2023
Angenommen nach Revision: 11. April 2023
Accepted Manuscript online:
11. April 2023
Artikel online veröffentlicht:
23. Mai 2023
© 2023. Thieme. All rights reserved
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References and Notes
- 1a Adhikari S, Orrit M. J. Chem. Phys. 2022; 156: 160903
- 1b Martinez-Moro M, Di Silvio D, Moya SE. Biophys. Chem. 2019; 253: 106218
- 2a Fang B, Shen Y, Peng B, Bai H, Wang L, Zhang J, Hu W, Fu L, Zhang W, Li L, Huang W. Angew. Chem. Int. Ed. 2022; 61: e202207188
- 2b Li H, Kim Y, Jung H, Hyun JY, Shin I. Chem. Soc. Rev. 2022; 51: 8957
- 3a Güixens-Gallardo P, Humpolickova J, Miclea SP, Pohl R, Kraus T, Jurkiewicz P, Hof M, Hocek M. Org. Biomol. Chem. 2020; 18: 912
- 3b Matyašovský J, Tack L, Palágyi A, Kuba M, Pohl R, Kraus T, Güixens-Gallardo P, Hocek M. Org. Biomol. Chem. 2021; 19: 9966
- 3c Ghosh P, Kropp HM, Betz K, Ludmann S, Diederichs K, Marx A, Srivatsan SG. J. Am. Chem. Soc. 2022; 144: 10556
- 3d Bai C, Klimkowski P, Jin C, Kuchlyan J, El-Sagheer AH, Brown T. Org. Biomol. Chem. 2022; 20: 8618
- 3e Kuba M, Pohl R, Kraus T, Hocek M. Bioconjugate Chem. 2023; 34: 133
- 4a Suzuki A, Yanaba T, Saito I, Saito Y. ChemBioChem 2014; 15: 1638
- 4b Suzuki A, Saito M, Katoh R, Saito Y. Org. Biomol. Chem. 2015; 13: 7459
- 4c Suzuki A, Yanagi M, Takeda T, Hudson RH. E, Saito Y. Org. Biomol. Chem. 2017; 15: 7853
- 4d Koboku S, Yanagi M, Funato A, Suzuki A, Saito Y. Tetrahedron Lett. 2020; 61: 151841
- 5a Murayama K, Asanuma H. ChemBioChem 2021; 22: 2507
- 5b Asanuma H, Kamiya Y, Kashida H, Murayama K. Chem. Commun. 2022; 58: 3993
- 6a Pudlo JS, Nassiri MR, Kern ER, Wotring LL, Drach JC, Townsend LB. J. Med. Chem. 1990; 33: 1984
- 6b Vandenriessche F, Snoeck R, Janssen G, Hoogmartens J, Van Aerschot A, De Clercq E, Herdewijn P. J. Med. Chem. 1992; 35: 1458
- 6c Vandendriessche F, Augustyns K, Van Aerschot A, Busson R, Hoogmartens J, Herdewijn P. Tetrahedron 1993; 49: 7223
- 7 Synthesis of 1 A mixture of 8 (36.1 mg, 0.10 mmol), Pd(PPh3)4 (46.2 mg, 4.0 × 10–2 mmol), CuI (7.6 mg, 4.0 × 10–2 mmol) and 2-naphthonitrile (24.7 mg, 0.14 mmol) in dry DMF (1.35 mL) and Et3N (0.36 mL) was stirred at 60 °C under an argon atmosphere for 1 h. After cooling to room temperature, the reaction mixture was concentrated in vacuo. The residue was purified by silica gel column chromatography, eluting with CHCl3/MeOH (15:1 to 5:1), to give 1 (25.1 mg, 61%) as a pale yellow solid. 1H NMR (400 MHz, DMSO-d 6): δ = 1.55 (m, 2 H), 1.91 (m, 1 H), 2.05 (m, 1 H), 3.45 (m, 2 H), 3.72 (m, 1 H), 4.37 (t, J = 4.4, 9.6 Hz, 1 H), 4.70–4.78 (complex, 2 H), 4.90 (m, 1 H), 7.37 (br s, 2 H), 7.82 (m, 2 H), 8.03 (s, 1 H), 8.09 (t, J = 9.2, 17.6 Hz, 2 H), 8.26 (s, 1 H), 8.30 (s, 1 H), 8.60 (s, 1 H). 13C NMR (100 MHz, DMSO-d 6): δ = 38.4, 46.9, 57.8, 65.2, 69.8, 88.1, 90.3, 92.8, 107.3, 108.8, 119.2, 123.8, 127.2, 129.0, 129.1, 129.4, 129.9, 131.0, 133.3, 134.1, 134.2, 140.9, 150.0, 154.6. HRMS (ESI): m/z [M + Na]+ calcd for C24H21N5O2Na: 434.1593; found: 434.1618.
- 8 Morris JV, Mahaney MA, Huber JR. J. Phys. Chem. 1976; 80: 969
Reviewed in:
Reviewed in:
Reviewed in: