Interaction between bioactive compound 11a-N-tosyl-5-deoxi-pterocarpan (LQB-223) and Calf thymus DNA: Spectroscopic approach, electrophoresis and theoretical studies

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• 作者：Marina M. Silva^a ; Eduarda O.O. Nascimento^a ; Edeí ; ldo F. Silva J&uacute ; nior^a ; Joã ; o Xavier de Ara&uacute ; jo J&uacute ; nior^a ; ^b ; Camilla C. Santana^b ; Luciano Aparecido M. Grillo^b ; Rafaela S. de Oliveira^c ; Paulo R.R.Costa^d ; Camilla D. Buarque^c ; Josué ; Carinhanha C. Santos^a ; ¹ ; ^{josue@iqb.ufal.br} ; ^{jcarinhanha@yahoo.com.br} ; Isis M. Figueiredo^a ; ¹ ; ^{figueiredo.isis@gmail.com}
• 关键词：11a-N-tosyl-5-carbapterocarpan ; 11a-N-arylsulfonyl-tetrahydro-5H-benzo[a]carbazole ; CT DNA interaction ; Spectroscopic techniques ; Theoretical studies ; Electrophoresis
• 刊名：International Journal of Biological Macromolecules
• 出版年：2017
• 出版时间：March 2017
• 年：2017
• 卷：96
• 期：Complete
• 页码：223-233
• 全文大小：2131 K
• 卷排序：96

文摘

The interaction of small molecules with DNA has been quite important, since this biomolecule is currently the major target for a wide range of drugs in clinical use or advanced clinical research phase. Thus, the present work aimed to assess the interaction process between the bioactive compound 11a-N-tosyl-5-carba-pterocarpan, (LQB-223), that presents antitumor activity, with DNA, employing spectroscopic techniques, electrophoresis, viscosity and theoretical studies. Through UV–vis and molecular fluorescence spectroscopy, it was possible to infer that the preferential quenching mechanism was static, characterized by non-fluorescent supramolecular complex formation between the LQB-223 and DNA. The binding constant was 1.94∙103 L mol−1 (30 °C) and, according to the thermodynamic parameters, the main forces involved in the interaction process are hydrophobic. Potassium iodide assay, competition with ethidium bromide, fluorescence contact energy transfer and melting temperature profile of DNA were employed to evaluate the binding mode. Except for KI assay, all results obtained indicated minor groove as the preferential binding mode of LQB-223 to DNA. These observations were supported by ionic strength assay, viscosity and molecular dynamics and docking studies. Finally, electrophoresis analysis demonstrated that the interaction does not promote DNA fragmentation, but it leads to variation in the migration profile after increasing the ligand concentration.