Department of Inorganic Chemistry, Faculty of Chemistry, Razi University, Kermanshah, Iran.
J Photochem Photobiol B. 2013 Nov 5;128:20-6. doi: 10.1016/j.jphotobiol.2013.08.005. Epub 2013 Aug 15.
The interaction of CT-DNA with the drug mesalamine (5-ASA) at physiological pH has been investigated by absorption, emission, circular dichroism (CD), cyclic voltammetry (CV), viscosity studies and molecular modeling. Thermodynamic parameters (ΔH>0 and ΔS<0) indicated that hydrogen bond and van der Waals play main roles in the binding of 5-ASA to CT-DNA. Ethidium bromide (EB) displacement studies revealed that 5-ASA did not have any effect on ethidium bromide (EB) bound DNA which is indicative of groove binding. The results obtained from experimental and molecular modeling showed that 5-ASA is a minor groove binder of DNA and preferentially binds to GC rich regions.
在生理 pH 值下,通过吸收、发射、圆二色性 (CD)、循环伏安法 (CV)、粘度研究和分子建模研究了 CT-DNA 与药物美沙拉嗪 (5-ASA) 的相互作用。热力学参数 (ΔH>0 和 ΔS<0) 表明,氢键和范德华力在 5-ASA 与 CT-DNA 的结合中起主要作用。溴化乙锭 (EB) 置换研究表明,5-ASA 对结合 DNA 的溴化乙锭 (EB) 没有任何影响,这表明其是沟槽结合。实验和分子建模得到的结果表明,5-ASA 是 DNA 的小沟结合物,优先与富含 GC 的区域结合。