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Surface-Enhanced Raman Scattering Based Nonfluorescent Probe for Multiplex DNA Detection

机译:基于表面增强拉曼散射的非荧光探针用于多重DNA检测

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摘要

To provide rapid and accurate detection of DNA markers in a straightforward, inexpensive and multiplex format, an alternative surface enhanced Raman scattering (SERS) based probe was designed and fabricated to covalently attach both DNA probing sequence and non-fluorescent Raman tags to the surface of gold nanoparticles (DNA-AuP-RTag). The intensity of Raman signal of the probes could be controlled through the surface coverage of the non-fluorescent Raman tags (RTags). Detection sensitivity of these probes could be optimized by fine-tuning the amount of DNA molecules and RTags on the probes. Long-term stability of the DNA-AuP-RTag probes was found to be good (over 3 months). Excellent multiplexing capability of the DNA-AuP-RTag scheme was demonstrated by simultaneous identification of up to eight probes in a mixture. Detection of hybridization of single-stranded DNA (ssDNA) to its complementary targets was successfully accomplished with a long-term goal to use non-fluorescent RTags in a Raman-based DNA microarray platform.
机译:为了以直接,廉价和多重的形式提供快速,准确的DNA标记检测,设计并制造了另一种基于表面增强拉曼散射(SERS)的探针,将DNA探测序列和非荧光拉曼标签共价连接到DNA表面。金纳米粒子(DNA-AuP-RTag)。探针的拉曼信号强度可以通过非荧光拉曼标签(RTag)的表面覆盖来控制。可以通过微调探针上的DNA分子和RTag的数量来优化这些探针的检测灵敏度。发现DNA-AuP-RTag探针的长期稳定性良好(超过3个月)。通过同时鉴定混合物中的多达八个探针,证明了DNA-AuP-RTag方案的出色的多路复用能力。单链DNA(ssDNA)与其互补靶标杂交的检测已成功完成,其长期目标是在基于拉曼的DNA微阵列平台中使用非荧光RTag。

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