Study by optical spectroscopy and molecular dynamics of the interaction of acridine-spermine conjugate with DNA

Autor: Francisca Sánchez-Jiménez, Aurelio A. Moya-García, S. Sánchez-Carrasco, Jean-Guy Delcros, Francisco J. Ramírez
Přispěvatelé: Facultad de Ciencias, Universidad de Málaga [Málaga] = University of Málaga [Málaga], Faculté de Medecine, Université de Rennes (UR)
Jazyk: angličtina
Rok vydání: 2008
Předmět:
Zdroj: Biophysical Chemistry
Biophysical Chemistry, 2008, 133 (1-3), pp.54. ⟨10.1016/j.bpc.2007.12.003⟩
ISSN: 0301-4622
DOI: 10.1016/j.bpc.2007.12.003⟩
Popis: We report a spectroscopic and theoretical study of the interaction between double-stranded oligonucleotides containing either adenine-thymine or guanine-cytosine alternating sequences and N1-(Acridin-9-ylcarbonyl)-1,5,9,14,18-pentazaoctadecane, or ASC, which is formed by the covalent bonding of spermine and 9-amidoacridine moieties via a trimethylene chain. Solutions containing the oligonucleotides and the conjugate at different molar ratios were studied using complementary spectroscopic techniques, including electronic absorption, fluorescence emission, circular dichroism, and Raman spectroscopy. The spectroscopical properties of ASC at both the vibrational and the electronic levels were described by means of ab initio quantum-chemical calculations on 9-amidoacridine, used as a model compound. Molecular dynamics calculations, based on the QM/MM methodology, were also performed using previously docked structures of two oligonucleotide-ASC complexes containing the A-T and the G-C sequence. Our data, taken all together, allowed us to demonstrate that conjugation of spermine to acridine modulates and gives additional properties to the interaction of the latter with DNA. As the ASC molecule has a high affinity by the polyamine transport system, these results are promising for their application in the development of new anti-tumour drugs.
Databáze: OpenAIRE
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