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Fluorescence Enhancement of Fluorophores Tethered to Different Sized Silver Colloids Deposited on Glass Substrate

机译:荧光团与沉积在玻璃基板上的不同尺寸的银胶体的荧光增强作用

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摘要

We studied fluorescence enhancements of fluorescein tethered to silver colloids of different size. Thiolated 23-mer oligonucleotide (ss DNA-SH) was bound selectively to silver colloids deposited on 3-aminopropyltriethoxysilane (APS)-treated quartz slides. Fluoresceinlabeled complementary oligonucleotide (ss Fl-DNA) was added in an amount significantly lower than the amount of unlabeled DNA tethered to the colloids. The hybridization kinetics, observed as an increase in fluorescence emission, on small (30-40 nm) and large (> 120 nm) colloids were similar. However, the final fluorescence intensity of the sample with large colloids was about 50% higher than that observed for the sample with small colloids. The reference sample without ss DNA-SH was used to estimate the fluorescence enhancements of fluorescein tethered to the small colloids (E = 2.7) and to the large colloids (E = 4.1) due to its steady fluorescence signal. The proposed method, based on controlled hybridization with minimal amount of fluorophore labeled ss DNA, can be used to reliably estimate the fluorescence enhancements on any silver nanostructures.
机译:我们研究了荧光素在不同大小的银胶体上的荧光增强作用。硫醇化的23-mer寡核苷酸(ss DNA-SH)与沉积在3-氨丙基三乙氧基硅烷(APS)处理的石英玻片上的银胶体选择性结合。加入荧光素标记的互补寡核苷酸(ss F1-DNA)的量显着低于拴系在胶体上的未标记DNA的量。在小的(30-40 nm)和大的(> 120 nm)胶体上观察到的荧光动力学增加的杂交动力学是相似的。但是,具有大胶体的样品的最终荧光强度比具有小胶体的样品的最终荧光强度高约50%。使用不含ss DNA-SH的参比样品,由于其稳定的荧光信号,被用来评估连接到小胶体(E = 2.7)和大胶体(E = 4.1)的荧光素的荧光增强。所提出的方法基于与最少量的荧光团标记的ss DNA的受控杂交,可用于可靠地估计任何银纳米结构上的荧光增强。

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