Faculty of Chemistry, University of Warsaw, 1 Pasteur St., 02-093 Warsaw, Poland.
Faculty of Chemistry, University of Warsaw, 1 Pasteur St., 02-093 Warsaw, Poland.
Spectrochim Acta A Mol Biomol Spectrosc. 2018 Oct 5;203:31-39. doi: 10.1016/j.saa.2018.05.076. Epub 2018 May 24.
Adsorption of molecules of DNA (deoxyribonucleic acid) or modified DNA on gold surfaces is often the first step in construction of many various biosensors, including biosensors for detection of DNA with a particular sequence. In this work we study the influence of amine and thiol modifications at the 3' ends of single stranded DNA (ssDNA) molecules on their adsorption on the surface of gold substrates and on the efficiency of hybridization of immobilized DNA with the complementary single stranded DNA. The characterization of formed layers has been carried out using infrared spectroscopy and atomic force microscopy. As model single stranded DNA we used DNA containing 20 adenine bases, whereas the complementary DNA contained 20 thymine bases. We found that the bands in polarization modulation-infrared reflection-adsorption spectroscopy (PM-IRRAS) spectra of layers formed from thiol-modified DNA are significantly narrower and sharper, indicating their higher regularity in the orientation of DNA on gold surface when using thiol linker. Also, hybridization of the layer of thiol-modified DNA containing 20 adenine bases with the respective DNA containing thymine bases leads to formation of much more organized structures than in the case of unmodified DNA or DNA with the amine linker. We conclude that the thiol-modified ssDNA is more promising for the preparation of biosensors, in comparison with the amine-modified or unmodified ssDNA. We have also found that the above-mentioned modifications at the 3' end of ssDNA significantly influence the IR spectrum (and hence the structure) of polycrystalline films formed from such compounds, even though adsorbed fragments contain less than 5% of the DNA chain. This effect should be taken into account when comparing IR spectra of various polycrystalline films formed from modified and unmodified DNA.
DNA(脱氧核糖核酸)或修饰 DNA 分子在金表面上的吸附通常是构建许多不同生物传感器的第一步,包括用于检测具有特定序列的 DNA 的生物传感器。在这项工作中,我们研究了单链 DNA(ssDNA)分子 3'末端的胺和巯基修饰对其在金基底表面吸附以及固定化 DNA 与互补单链 DNA 杂交效率的影响。形成的层的特性是使用红外光谱和原子力显微镜进行的。作为模型单链 DNA,我们使用含有 20 个腺嘌呤碱基的 DNA,而互补 DNA 含有 20 个胸腺嘧啶碱基。我们发现,来自巯基修饰 DNA 的层的偏振调制红外反射吸收光谱(PM-IRRAS)谱中的带明显更窄和更尖锐,表明当使用巯基接头时,DNA 在金表面上的取向更规则。此外,含 20 个腺嘌呤碱基的巯基修饰 DNA 层与含胸腺嘧啶碱基的相应 DNA 的杂交导致形成的结构比未修饰 DNA 或含胺接头的 DNA 更为有序。我们得出结论,与未修饰或胺修饰的 ssDNA 相比,巯基修饰的 ssDNA 更适合制备生物传感器。我们还发现,ssDNA 3'末端的上述修饰会显著影响由这些化合物形成的多晶薄膜的红外光谱(因此也影响结构),即使吸附的片段仅含有 DNA 链的不到 5%。在比较由修饰和未修饰 DNA 形成的各种多晶薄膜的红外光谱时,应考虑到这种影响。