عنوان
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Exploring the binding mechanism of saccharin and sodium saccharin to
promoter of human p53 gene by theoretical and experimental methods
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نوع پژوهش
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مقاله چاپشده در مجلات علمی
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کلیدواژهها
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Saccharin; promoter of human p53 gene; fluorescence spectroscopic; molecular dynamics simulation; DNA-binding properties; docking; cancer; MM/PBSA binding free energy
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چکیده
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In the past few decades, extensive discussions have been on the impact of artificial sweeteners on the risk of cancer. The present study aimed to evaluate the interaction of saccharin (SA) and sodium saccharin (SSA) with the promoter of the human p53 gene. The binding ability was assessed using the spectroscopic technique, molecular docking and molecular dynamics (MD) simulation methods. Free energy of binding has been calculated using Molecular Mechanics/Poisson–Boltzmann Surface Area (MM/PBSA) method. Fluorescence spectra of mentioned gene with concentration profiles of SA and SSA were obtained in a physiological condition. A gradual increase without any significant spectral shift in the fluorescence intensity of around 350 nm was evident, indicating the presence of an interaction between both compounds and gene. The docking results showed that both compounds were susceptible to bind to 50 -DG56DG57-30 nucleotide sequence of gene. Furthermore, the MD simulation demonstrated that the binding positions for SA and SSA were 50 -A1T3T4-30 and 50 -G44T45-30 sequences of gene, respectively. The binding of these sweeteners to gene made significant conformational changes to the DNA structure. Hydrogen and hydrophobic interactions are the major forces in complexes stability. Through the groove binding mode, the non-interactive DNA-binding nature of SSA and SA has been demonstrated by the results of spectrofluorometric and molecular modeling. This study could provide valuable insight into the binding mechanism of SA and its salt with p53 gene promoter as macromolecule at the molecular level in atomistic details. This work can contribute to the possibility of the potential hazard of carcinogenicity of this sweetener and to design and apply new and safer artificial sweeteners.
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پژوهشگران
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محبوبه منصوریان (نفر اول)، کریم مهنام (نفر دوم)، حمیدرضا رجبی (نفر سوم)، محمود روشنی (نفر چهارم)، امیرحسین دوستی مطلق (نفر پنجم)
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