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Tuning Two-Photon Photoluminescence of Gold Nanoparticle Aggregates with DNA and Its Application as Turn-on Photoluminescence Probe for DNA Sequence Detection

机译:DNA调节金纳米粒子聚集体的双光子光致发光及其在开启光致发光探针中的应用

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Plasmon coupling between noble metal nanoparticles has been known to dramatically enhance linear and nonlinear optical properties of nearby chromophores and metal nanoparticles themselves. The interparticle distance is expected to have significant influence on the coupling strength. Here we have prepared DNA tuned Au nanoparticle assemblies with well controlled separation distances from 2.0 to 12.2 irai to investigate plasmon coupling strength and particle size effects on two-photon photoluminescence (TPPL) enhancement. TPPL intensities of these DNA coupled nanoassemblies were found to increase rapidly as the separation distance decreases. The largest TPPL enhancement factors of 115 and 265 were achieved at the shortest available separation distance of 2.0 nm for 21 and 41 nm Au NPs-dsDNA assemblies, respectively. We have further utilized DNA induced coupling of Au NPs and TPPL enhancement to develop a two-photon sensing scheme for detection of DNA sequences. This TPPL based method displayed high sensitivity with a limit of detection of 2.9 pM and excellent selectivity against ssDNA with mismatched bases. A single mismatch can be easily differentiated at room temperature. Taking the unique advantages of two-photon excitation, this method could be potentially further extended to DNA detection inside cells or even in vivo. These findings can provide important insight for fundamental understanding of plasmon-coupling enhanced TPPL and development of various two-photon excitation based applications.
机译:已知贵金属纳米粒子之间的等离子耦合可显着增强附近的生色团和金属纳米粒子本身的线性和非线性光学性质。预计粒子间距离将对耦合强度产生重大影响。在这里,我们准备了DNA调谐的金纳米粒子组件,其分离距离从2.0到12.2 irai受到很好的控制,以研究等离子体耦合强度和粒径对双光子光致发光(TPPL)增强的影响。发现这些DNA偶联纳米组件的TPPL强度随着分离距离的减小而迅速增加。分别在21和41 nm Au NPs-dsDNA组件的最短可用分离距离2.0 nm处实现了115和265的最大TPPL增强因子。我们进一步利用DNA诱导的Au NPs和TPPL增强的偶联来开发用于检测DNA序列的双光子传感方案。这种基于TPPL的方法显示出高灵敏度,检测限为2.9 pM,并且对碱基不匹配的ssDNA具有出色的选择性。在室温下可以轻松地区分单个失配。利用双光子激发的独特优势,该方法可以潜在地进一步扩展到细胞内部甚至体内的DNA检测。这些发现可为对等离激元耦合增强的TPPL和各种基于双光子激发的应用开发的基础理解提供重要的见识。

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