Dipartimento di Scienze Fisiche, Complesso Universitario, Universitá di Napoli Federico II, Monte S. Angelo, Via Cinthia, I-80126 Napoli, Italy.
Anal Chem. 2011 Sep 1;83(17):6849-55. doi: 10.1021/ac201783h. Epub 2011 Aug 9.
In this work, we establish the use of surface-enhanced Raman scattering (SERS) as a label-free analytical technique for the direct detection of G-quadruplex formation. In particular, we demonstrate that SERS analysis allows the evaluation of the relative stability of G quadruplexes that differ for the number of G tetrads and investigate several structural features of quadruplexes, such as the orientation of glycosidic bonds, the identification of distortions in the sugar-phosphate backbone, and the degree of hydrogen-bond solvation. Herein, the fluctuation of the SERS spectra, due to the specific interaction of vibrational modes with the SERS-active substrate, is quantitatively analyzed before and after quadruplex formation. The results of this study suggest a perpendicular orientation of the quadruplexes (with or without the 3'-tetra end linker) with respect to the silver colloidal surface, which opens new perspectives for the use of SERS as a label-free analytical tool for the study of the binding mode between quadruplexes and their ligands.
在这项工作中,我们建立了表面增强拉曼散射(SERS)作为一种无标记分析技术,用于直接检测 G-四链体的形成。特别是,我们证明了 SERS 分析可以评估 G 四链体的相对稳定性,这些稳定性因 G 四联体的数量而异,并研究了四链体的几个结构特征,如糖苷键的取向、糖-磷酸骨架的扭曲以及氢键溶剂化的程度。在此,通过在四链体形成前后对 SERS 光谱的波动进行定量分析,研究了振动模式与 SERS 活性基底的特定相互作用。本研究的结果表明,四链体(无论是否带有 3'-四末端接头)与银胶体表面呈垂直取向,这为 SERS 作为一种无标记分析工具用于研究四链体与其配体之间的结合模式开辟了新的前景。