Pershina A G, Sazonov A E, Ogorodova L M
State Education Institute of Higher Professional Education, Siberian State Medical University, Roszdrav, Moscow Trakt 2, Tomsk, Russia.
Bioorg Khim. 2009 Sep-Oct;35(5):674-80. doi: 10.1134/s1068162009050112.
The interaction of DNA with nanoparticles of cobalt ferrite powder prepared by the mechano-chemical method was studied. It was shown that CoFe(2)O(4) nanoparticles efficiently bind DNA in aqueous solutions (Tris-HCl), forming a bionanocomposite. The adsorption capacity of CoFe(2)O(4) nanoparticles for DNA was evaluated to be 5.25 x 10(-3) mol/m(2). The desorption of DNA from the surface of the particles was analyzed while changing the pH, the ionic strength, and the chemical content of the medium. The DNA-CoFe(2)O(4) nanocomposite was investigated by FTIR spectroscopy. The block of the data allowed one to consider the mechanism of the interaction between a polynucleotide and CoFe(2)O(4) nanoparticles and to make the assumption that the binding occurred due to the coordination interaction of the phosphate groups and heterocyclic bases of DNA (oxygen atoms of thymine and guanine) with metal ions on the particle surface. The analysis of the IR spectra showed that binding can lead to the partial destabilization of the DNA structure, with the B conformation of a polynucleotide being preserved.
研究了DNA与通过机械化学方法制备的钴铁氧体粉末纳米颗粒之间的相互作用。结果表明,CoFe₂O₄纳米颗粒在水溶液(Tris-HCl)中能有效结合DNA,形成生物纳米复合材料。CoFe₂O₄纳米颗粒对DNA的吸附容量经评估为5.25×10⁻³ mol/m²。在改变pH值、离子强度和介质化学组成的情况下,分析了DNA从颗粒表面的解吸情况。通过傅里叶变换红外光谱(FTIR)对DNA-CoFe₂O₄纳米复合材料进行了研究。数据处理使人们能够考虑多核苷酸与CoFe₂O₄纳米颗粒之间的相互作用机制,并假设这种结合是由于DNA的磷酸基团和杂环碱基(胸腺嘧啶和鸟嘌呤的氧原子)与颗粒表面的金属离子之间的配位相互作用而发生的。红外光谱分析表明,结合可能导致DNA结构的部分不稳定,同时多核苷酸的B构象得以保留。