Departamento de Química Fisica e Inorganica, Universitat Rovira i Virgili and Centro de Tecnologia Química, Carrer de Marcel lí Domingo s/n, 43007 Tarragona (Spain); Medcom Advance SA, Viladecans Bussines Park, Edificio Brasil, C/Bertran i Musitu, 83-85, 08840 Viladecans (Barcelona) (Spain).
Angew Chem Int Ed Engl. 2015 Jan 19;54(4):1144-8. doi: 10.1002/anie.201408558. Epub 2014 Nov 20.
The exploration of the genetic information carried by DNA has become a major scientific challenge. Routine DNA analysis, such as PCR, still suffers from important intrinsic limitations. Surface-enhanced Raman spectroscopy (SERS) has emerged as an outstanding opportunity for the development of DNA analysis, but its application to duplexes (dsDNA) has been largely hampered by reproducibility and/or sensitivity issues. A simple strategy is presented to perform ultrasensitive direct label-free analysis of unmodified dsDNA with the means of SERS by using positively charged silver colloids. Electrostatic adhesion of DNA promotes nanoparticle aggregation into stable clusters yielding intense and reproducible SERS spectra at nanogram level. As potential applications, we report the quantitative recognition of hybridization events as well as the first examples of SERS recognition of single base mismatches and base methylations (5-methylated cytosine and N6-methylated Adenine) in duplexes.
对 DNA 所携带的遗传信息的探索已成为一项重大的科学挑战。常规的 DNA 分析,如 PCR,仍然存在着重要的固有局限性。表面增强拉曼光谱(SERS)的出现为 DNA 分析的发展提供了一个极好的机会,但由于重现性和/或灵敏度问题,其在双链 DNA(dsDNA)中的应用受到了很大的限制。本文提出了一种简单的策略,通过使用带正电荷的银胶体,利用 SERS 对未经修饰的 dsDNA 进行超灵敏的直接无标记分析。DNA 的静电附着促进了纳米颗粒的聚集,形成稳定的簇,从而在纳克水平上产生强烈且可重现的 SERS 光谱。作为潜在的应用,我们报告了杂交事件的定量识别,以及 SERS 对双链体中单碱基错配和碱基甲基化(5-甲基胞嘧啶和 N6-甲基腺嘌呤)的首次识别实例。