Synthesis of a bisbenzoxazole analogue of Hoechst 33258 as a Potential GC-Selective Dna Ligand
- Авторлар: Arutuynyan A.F.1, Aksenova M.S.1, Kostyukov A.A.2, Stomakhin A.A.1, Kaluzhny D.N.1, Zhuze A.L.1
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Мекемелер:
- Engelhardt Institute of Molecular Biology, Russian Academy of Sciences
- Emanuel Institute of Biochemical Physics, Russian Academy of Science
- Шығарылым: Том 58, № 3 (2024)
- Беттер: 482-492
- Бөлім: СТРУКТУРНО-ФУНКЦИОНАЛЬНЫЙ АНАЛИЗ БИОПОЛИМЕРОВИ ИХ КОМПЛЕКСОВ
- URL: https://edgccjournal.org/0026-8984/article/view/655323
- DOI: https://doi.org/10.31857/S0026898424030123
- EDN: https://elibrary.ru/JCCURC
- ID: 655323
Дәйексөз келтіру
Аннотация
Using a computer modelling approach we proposed the structure of a potential GC-specific DNA ligand, which could form a complex with DNA in the minor groove similar to that formed by Hoechst 33258 at DNA AT-enriched sites. According to this model MBoz2A, a bisbenzoxazole ligand, was synthesized. The results of spectrophotometric methods supported the complex formation of the compound under study with DNA differed in the nucleotide composition.
Толық мәтін

Авторлар туралы
A. Arutuynyan
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences
Email: zhuze@eimb.ru
Ресей, Moscow, 119991
M. Aksenova
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences
Email: zhuze@eimb.ru
Ресей, Moscow, 119991
A. Kostyukov
Emanuel Institute of Biochemical Physics, Russian Academy of Science
Email: zhuze@eimb.ru
Ресей, Moscow, 119334
A. Stomakhin
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences
Email: zhuze@eimb.ru
Ресей, Moscow, 119991
D. Kaluzhny
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences
Email: zhuze@eimb.ru
Ресей, Moscow, 119991
A. Zhuze
Engelhardt Institute of Molecular Biology, Russian Academy of Sciences
Хат алмасуға жауапты Автор.
Email: zhuze@eimb.ru
Ресей, Moscow, 119991
Әдебиет тізімі
- Geierstanger B.H., Wemmer D.E. (1995) Complexes of the minor groove of DNA. Annu. Rev. Biophys. Biomol. Structure. 24, 463–493.
- Krey A.K., Hahn F.E. (1970) Studies on the complex of distamycin A with calf thymus DNA. FEBS Lett. 10, 175–178.
- Harshman K.D., Dervan P.B. (1985) Molecular recognition of B-DNA by Hoechst 33258. Nucl. Acids Res. 13, 4825–48354.
- Dervan P.B. (2001) Molecular recognition of DNA by small molecules. Bioorg. Med. Chem. 9, 2215–2235.
- Dervan P.B., Buerli R.W. (1999) Sequence-specific DNA recognition by polyamides. Curr. Opin. Chem. Biol. 3, 688–693.
- Wemmer D.E., Dervan P.B. (1997) Targeting the minor groove of DNA. Curr. Opin. Struct. Biol. 7, 355–361.
- Dervan P.B., Doss R.M., Marques M.A. (2005) Programmable DNA binding oligomers for control of transcription. Curr. Med. Chem. Anti-Cancer Agents. 5, 373–387.
- Guo P., Paul A., Kumar A., Farahat A.A., Kumar D., Wang S., Boykin D.W., Wilson D.W. (2016) The thiophene “sigma-hole” as a concept for preorganized, specific recognition of G.C base pairs in the DNA minor groove. Chem. Eur. J. 22, 15404–15412.
- Guo P., Farahat A.A., Paul A., Hanka N.K., Boykin D.V., Wilson W.D. (2018) Compound shape effects in minor groove binding affinity and specificity for mixed sequence DNA. J. Am. Chem. Soc. 140, 14761–14769.
- Wilson W.D., Paul A. (2023) Compound shape and substituent effects in DNA minor groove interactions. In: Handbook of Chemical Biology of Nucleic Acids. Еd. Sugimoto N. Singapore: Springer, pp. 1‒39.
- Paul A., Nanjunda R., Wilson W.D. (2023) Binding to the DNA minor groove by heterocyclic dications from AT specific to GC recognition compounds. Curr. Protocols. 3(4), e729.
- O’Boyle N.M., Banck M., Craig A.J., Morley C., Vandermeersch T., Hutchison G.R. (2011) Open Babel: an open chemical toolbox. J. Cheminformatics. 3, 1–14.
- Korb O., Stützle T., Exner T.E. (2007) An ant colony optimization approach to flexible protein–ligand docking. Swarm Intelligence. 1, 115134.
- Teng M.K., Usman N., Frederick C.A., Wang A.H. (1988) The molecular structure of the complex of Hoechst 33258 and the DNA dodecamer d (CGCGAATTCGCG). Nucl. Acids Res. 16, 2671–2690.
- Finlay A.C., Hochstein F.A., Sobin B.A., Murphy F.X. (1951) Netropsin, a new antibiotic produced by a Streptomyces. J. Am. Chem. Soc. 73, 341–344.
- Zasedatelev A.S., Borodulin V.B., Grokhovsky S.L., Nikitin A.M., Salmanova D.V., Zhuze A.L., Gursky G.V., Shafer R.H. (1995) Mono-, di- and trimeric binding of a bis-netropsin to DNA. FEBS Lett. 375, 304–306.
- Makarska-Bialokoz M. (2014) Fluorescence quenching effect of guanine interacting with water-soluble cationic porphyrin. J. Luminescence. 47, 27–33.
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