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Binding site identification of anticancer drug gefitinib to HSA and DNA in the presence of five different probes.
Tanzadehpanah, Hamid; Mahaki, Hanie; Moghadam, Neda Hosseinpour; Salehzadeh, Sadegh; Rajabi, Omid; Najafi, Rezvan; Amini, Razieh; Saidijam, Massoud.
Afiliación
  • Tanzadehpanah H; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Mahaki H; b Department of Immunology, School of Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Moghadam NH; c Faculty of Chemistry , Bu-Ali Sina University , Hamedan , Iran.
  • Salehzadeh S; c Faculty of Chemistry , Bu-Ali Sina University , Hamedan , Iran.
  • Rajabi O; d Medical Chemistry Department, School of Pharmacy , Mashhad University of Medical Sciences , Mashhad , Iran.
  • Najafi R; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Amini R; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
  • Saidijam M; a Research Center for Molecular Medicine , Hamadan University of Medical Sciences , Hamadan , Iran.
J Biomol Struct Dyn ; 37(4): 823-836, 2019 03.
Article en En | MEDLINE | ID: mdl-29447084
This study was carried out to evaluate the binding interaction of gefitinib (GEF) with human serum albumin (HSA) and calf thymus DNA (ct-DNA) using fluorescence, UV-Visible, zeta potential measurements and molecular docking methods in order to understand its pharmacokinetic mechanism. By increasing the temperature, a steady decrease in Stern-Volmer quenching constants was observed for HSA binding properties; this indicates a static type of fluorescence quenching. Negative values were calculated for Gibbs free energy (ΔG), enthalpy (ΔH), and entropy (ΔS) changes, indicating that the reaction is spontaneous and enthalpy-driven. Probe competitive experimental results showed that GEF contains the same binding site as warfarin and are consistent with modeling results. The zeta potential of the HSA increased with increasing GEF, which represents the presence of electrostatic interactions in the system. DNA binding properties were investigated in the presence of three probes. The experimental results showed that by increasing GEF to DNA-AO (acridine-orange) and DNA-MB (methylene-blue) system, the fluorescence intensity and absorbance spectra had no considerable change. Furthermore, with the addition of GEF to DNA, the zeta potential decreased gradually, indicating that the hydrophobic interaction between the GEF and the bases of DNA is the major factor. Thus, GEF can bind to DNA via a groove binding mode. It was also found that GEF entered into the minor groove in the A-T rich region of DNA fragment and bind via van der-Waals forces and three H-bond with double strands of DNA. This is in good agreement with experimental results.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Albúmina Sérica Humana / Gefitinib / Antineoplásicos Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Biomol Struct Dyn Año: 2019 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN / Albúmina Sérica Humana / Gefitinib / Antineoplásicos Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: J Biomol Struct Dyn Año: 2019 Tipo del documento: Article País de afiliación: Irán Pais de publicación: Reino Unido