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Direct Approach toward Label-Free DNA Detection by Surface-Enhanced Raman Spectroscopy: Discrimination of a Single-Base Mutation in 50 Base-Paired Double Helixes.
Analytical Chemistry ( IF 6.7 ) Pub Date : 2019-06-19 00:00:00 , DOI: 10.1021/acs.analchem.9b01887
Yang Li 1 , Tianyang Gao 1 , Guantong Xu 1 , Xiaoxuan Xiang 1 , Bing Zhao 1 , Xiao Xia Han 1 , Xinhua Guo 1, 2
Affiliation  

Surface-enhanced Raman spectroscopy (SERS) has exhibited great potential in label-free DNA detection. Owing to the limitation in chain length, it is however still challenging for SERS as a routine method to explore the intrinsic structural information on unmodified DNA. Here, we develop a universal SERS-based approach toward quantification of A/G in single-stranded DNAs (12 up to 28 bases) by introducing a novel interfacial agent, dichloromethane. DNA hybridization is successfully probed as evidenced by the typical SERS bands attributed to hydrogen bonds in a hairpin structure. More importantly, enlarged space of “hot spots” in SERS enables discrimination of single-base mutation in double-stranded DNA with 100 bases, which as a proof-of-concept study will pave a new avenue for highly sensitive DNA detection in clinical applications.

中文翻译:

通过表面增强拉曼光谱法检测无标签DNA的直接方法:区分50个碱基配对的双螺旋中的单碱基突变。

表面增强拉曼光谱(SERS)在无标记DNA检测中显示出巨大潜力。由于链长的限制,作为常规方法,SERS仍是探索未修饰DNA固有结构信息的挑战。在这里,我们通过引入新型界面剂二氯甲烷,开发了一种基于通用SERS的方法来定量单链DNA(12至28个碱基)中的A / G。DNA杂交已成功探查,这可归因于发夹结构中氢键的典型SERS条带。更重要的是,SERS中“热点”的扩大空间可区分具有100个碱基的双链DNA中的单碱基突变,这作为概念验证研究将为临床应用中的高灵敏度DNA检测铺平道路。
更新日期:2019-06-19
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