Mustafa Alp Özkul , Tunahan Akgül , Mehmet Şerif Bozaslan , Suleyman Can Toksoy , Gökhan Dikmen
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DNA binding studies also provide critical information to optimize the effects of antifungal drugs on target cells and to increase the selective toxicity of drugs. Ketoconazole (KTZ) is an azole-containing antifungal drug, and azole-containing drugs have many pharmacological properties. In this study, the interaction between the KTZ molecule and calf-thymus DNA (ct-DNA) was examined using various spectroscopic methods. The binding constant between ct-DNA and KTZ molecule was calculated using results obtained from different spectroscopic methods. UV–vis and fluorescence studies indicated a binding constant was calculated as 5.8 × 10<sup>4</sup> M<sup>−1</sup> and 6.21 × 10<sup>4</sup> M<sup>−1</sup> for the interaction between KTZ and ct-DNA, respectively. ct-DNA quenched the fluorescence of KTZ with a quenching constant approximately equal to 13 × 10<sup>12</sup> M<sup>−1</sup>.s<sup>−1</sup>. Fluorescence displacement experiments using ethidium bromide (EB) and Hoechst 33,258 revealed interaction between KTZ and ct-DNA occurred through minor groove binding mode. This conclusion was further supported by viscosity measurements, DNA melting studies, and KI quenching experiments. In light of experimental results, KTZ molecule quenches the fluorescence of DNA with a static mechanism due to the negative values of thermodynamic parameters such as ΔH<sup>o</sup> and ΔS<sup>o</sup>. In addition, the interaction of the KTZ molecule with ct-DNA was investigated theoretically by Molecular Docking. It interacts with the minor groove of DNA through a combination of van der Waals forces and hydrogen bonding interactions.</div></div>","PeriodicalId":433,"journal":{"name":"Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy","volume":"341 ","pages":"Article 126351"},"PeriodicalIF":4.3000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"DNA binding study of antifungal drug Ketoconazole by molecular docking and spectroscopic analysis\",\"authors\":\"Mustafa Alp Özkul , Tunahan Akgül , Mehmet Şerif Bozaslan , Suleyman Can Toksoy , Gökhan Dikmen\",\"doi\":\"10.1016/j.saa.2025.126351\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The process of developing new drug molecules is long-term, costly, and especially the process of moving to clinical trials takes a long time. Consequently, conducting experimental and theoretical binding studies of drugs or drug candidates with biological materials, such as DNA and RNA, are crucial to reduce costs and minimize time requirements. As the DNA a fundamental biological molecule constitutes a major target for numerous pharmaceuticals, binding studies of various molecules with DNA is a broad field of research. DNA binding properties of antifungal drugs are of great importance in understanding their biological activities and elucidating their mechanisms of action. DNA binding studies also provide critical information to optimize the effects of antifungal drugs on target cells and to increase the selective toxicity of drugs. Ketoconazole (KTZ) is an azole-containing antifungal drug, and azole-containing drugs have many pharmacological properties. In this study, the interaction between the KTZ molecule and calf-thymus DNA (ct-DNA) was examined using various spectroscopic methods. The binding constant between ct-DNA and KTZ molecule was calculated using results obtained from different spectroscopic methods. UV–vis and fluorescence studies indicated a binding constant was calculated as 5.8 × 10<sup>4</sup> M<sup>−1</sup> and 6.21 × 10<sup>4</sup> M<sup>−1</sup> for the interaction between KTZ and ct-DNA, respectively. ct-DNA quenched the fluorescence of KTZ with a quenching constant approximately equal to 13 × 10<sup>12</sup> M<sup>−1</sup>.s<sup>−1</sup>. Fluorescence displacement experiments using ethidium bromide (EB) and Hoechst 33,258 revealed interaction between KTZ and ct-DNA occurred through minor groove binding mode. This conclusion was further supported by viscosity measurements, DNA melting studies, and KI quenching experiments. In light of experimental results, KTZ molecule quenches the fluorescence of DNA with a static mechanism due to the negative values of thermodynamic parameters such as ΔH<sup>o</sup> and ΔS<sup>o</sup>. 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引用次数: 0
摘要
开发新药物分子的过程是长期的,昂贵的,特别是进入临床试验的过程需要很长时间。因此,进行药物或候选药物与生物材料(如DNA和RNA)结合的实验和理论研究对于降低成本和最小化时间要求至关重要。由于DNA是一种基本的生物分子,是许多药物的主要靶点,因此各种分子与DNA结合的研究是一个广泛的研究领域。抗真菌药物的DNA结合特性对了解其生物活性和阐明其作用机制具有重要意义。DNA结合研究也为优化抗真菌药物对靶细胞的作用和增加药物的选择性毒性提供了重要信息。酮康唑(KTZ)是一种含唑类抗真菌药物,含唑类药物具有许多药理性质。本研究利用各种光谱方法研究了KTZ分子与小牛胸腺DNA (ct-DNA)之间的相互作用。利用不同光谱方法的结果计算了ct-DNA与KTZ分子的结合常数。紫外-可见和荧光研究表明,KTZ与ct-DNA相互作用的结合常数分别为5.8 × 104 M - 1和6.21 × 104 M - 1。ct-DNA猝灭KTZ荧光,猝灭常数约为13 × 1012 M−1.s−1。利用溴化乙啶(EB)和Hoechst 33,258进行的荧光位移实验表明,KTZ与ct-DNA的相互作用是通过轻微的凹槽结合模式发生的。这一结论进一步得到了粘度测量、DNA熔化研究和KI淬火实验的支持。实验结果表明,由于ΔHo和ΔSo等热力学参数为负值,KTZ分子以静态机制猝灭DNA的荧光。此外,通过分子对接理论研究了KTZ分子与ct-DNA的相互作用。它通过范德华力和氢键相互作用与DNA的小凹槽相互作用。
DNA binding study of antifungal drug Ketoconazole by molecular docking and spectroscopic analysis
The process of developing new drug molecules is long-term, costly, and especially the process of moving to clinical trials takes a long time. Consequently, conducting experimental and theoretical binding studies of drugs or drug candidates with biological materials, such as DNA and RNA, are crucial to reduce costs and minimize time requirements. As the DNA a fundamental biological molecule constitutes a major target for numerous pharmaceuticals, binding studies of various molecules with DNA is a broad field of research. DNA binding properties of antifungal drugs are of great importance in understanding their biological activities and elucidating their mechanisms of action. DNA binding studies also provide critical information to optimize the effects of antifungal drugs on target cells and to increase the selective toxicity of drugs. Ketoconazole (KTZ) is an azole-containing antifungal drug, and azole-containing drugs have many pharmacological properties. In this study, the interaction between the KTZ molecule and calf-thymus DNA (ct-DNA) was examined using various spectroscopic methods. The binding constant between ct-DNA and KTZ molecule was calculated using results obtained from different spectroscopic methods. UV–vis and fluorescence studies indicated a binding constant was calculated as 5.8 × 104 M−1 and 6.21 × 104 M−1 for the interaction between KTZ and ct-DNA, respectively. ct-DNA quenched the fluorescence of KTZ with a quenching constant approximately equal to 13 × 1012 M−1.s−1. Fluorescence displacement experiments using ethidium bromide (EB) and Hoechst 33,258 revealed interaction between KTZ and ct-DNA occurred through minor groove binding mode. This conclusion was further supported by viscosity measurements, DNA melting studies, and KI quenching experiments. In light of experimental results, KTZ molecule quenches the fluorescence of DNA with a static mechanism due to the negative values of thermodynamic parameters such as ΔHo and ΔSo. In addition, the interaction of the KTZ molecule with ct-DNA was investigated theoretically by Molecular Docking. It interacts with the minor groove of DNA through a combination of van der Waals forces and hydrogen bonding interactions.
期刊介绍:
Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy (SAA) is an interdisciplinary journal which spans from basic to applied aspects of optical spectroscopy in chemistry, medicine, biology, and materials science.
The journal publishes original scientific papers that feature high-quality spectroscopic data and analysis. From the broad range of optical spectroscopies, the emphasis is on electronic, vibrational or rotational spectra of molecules, rather than on spectroscopy based on magnetic moments.
Criteria for publication in SAA are novelty, uniqueness, and outstanding quality. Routine applications of spectroscopic techniques and computational methods are not appropriate.
Topics of particular interest of Spectrochimica Acta Part A include, but are not limited to:
Spectroscopy and dynamics of bioanalytical, biomedical, environmental, and atmospheric sciences,
Novel experimental techniques or instrumentation for molecular spectroscopy,
Novel theoretical and computational methods,
Novel applications in photochemistry and photobiology,
Novel interpretational approaches as well as advances in data analysis based on electronic or vibrational spectroscopy.