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Surface-enhanced Raman scattering for discovering and scoring single-base differences in DNA

机译:表面增强拉曼散射,用于发现和评分DNA中的单碱基差异

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Abstract: Information about DNA sequence variation is increasingly being recognized as an important tool in the analysis of many diseases and in the development of diagnostic, therapeutic, and preventive strategies. Surface enhanced Raman scattering (SERS) is suggested as a new, potentially powerful method for detection and identification of single base differences in double stranded DNA fragments. Enhanced Raman signal is originated from nucleotides that are in direct contact with SERS active metal surface. Aromatic rings in double stranded perfectly matched DNA are hydrogen bonded and do not interact with the metal. In the case of an insertion, deletion or base mismatch, hydrogen bonding is disrupted and an open region is formed. Raman scattering from base pairs in this region undergoes an enhancement resulting in SERS spectrum. Model experiments were performed with 209 base pairs DNA fragment containing one mismatch and adsorbed on electrochemically roughened silver surface. A fragment of the same length but without mismatch was used as a control. No spectra were obtained from the control adsorbed on the SERS substrate, whereas the sample with one mismatch yielded a distinct SERS spectrum. It is believed that all bands in the spectrum correspond to the mismatched base pair and bases from the closest environment around the mismatch. !25
机译:摘要:关于DNA序列变异的信息越来越多地被认为是分析许多疾病以及发展诊断,治疗和预防策略的重要工具。建议将表面增强拉曼散射(SERS)作为检测和鉴定双链DNA片段中单碱基差异的潜在新方法。增强的拉曼信号源自与SERS活性金属表面直接接触的核苷酸。双链完美匹配的DNA中的芳香环是氢键,不与金属相互作用。在插入,缺失或碱基错配的情况下,氢键被破坏并且形成开放区域。来自该区域中的碱基对的拉曼散射经历增强,从而产生SERS光谱。用含有一个错配并吸附在电化学粗糙银表面上的209个碱基对的DNA片段进行了模型实验。使用相同长度但没有错配的片段作为对照。从吸附在SERS底物上的对照没有获得光谱,而具有一个不匹配的样品产生了独特的SERS光谱。可以相信,频谱中的所有谱带都对应于错配的碱基对和错配周围最近的碱基。 !25

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