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Increasing the sensitivity of DNA microarrays by metal-enhanced fluorescence using surface-bound silver nanoparticles

机译:使用表面结合的银纳米颗粒增加金属增强荧光的DNA微阵列的敏感性

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The effects of metal-enhanced fluorescence (MEF) have been measured for two dyes commonly used in DNA microarrays, Cy3 and Cy5. Silver island films (SIFs) grown on glass microscope slides were used as substrates for MEF DNA arrays. We examined MEF by spotting biotinylated, singly-labeled 23 bp DNAs onto avidin-coated SIF substrates. The fluorescence enhancement was found to be dependent on the DNA spotting concentration: below ~12.5 μM, MEF increased linearly, and at higher concentrations MEF remained at a constant maximum of 28-fold for Cy5 and 4-fold for Cy3, compared to avidin-coated glass substrates. Hybridization of singly-labeled oligonucleotides to arrayed single-stranded probes showed lower maximal MEF factors of 10-fold for Cy5 and 2.5-fold for Cy3, because of the smaller amount of immobilized fluorophores as a result of reduced surface hybridization efficiencies. We discuss how MEF can be used to increase the sensitivity of DNA arrays, especially for far red emitting fluorophores like Cy5, without significantly altering current microarray protocols.
机译:已经测量了金属增强荧光(MEF)的效果,用于DNA微阵列,CY3和CY5中常用的两种染料。在玻璃显微镜载玻片上生长的银岛薄膜(SIFS)用作MEF DNA阵列的底物。通过将生物素化的,单标记的23bp dNA分析到抗生物素蛋白涂覆的SIF基板上,检查MEF。发现荧光增强依赖于DNA斑点浓度:低于〜12.5μm,MeF线性增加,与抗生物素蛋白相比,MeF在较高浓度的MeF下保持恒定的最大28倍,4倍为4倍。涂层玻璃基板。单标记的单链探针的单标记寡核苷酸的杂交显示出较低的MEF因子10倍的CY5和2.5倍的CY3,因为由于表面杂交效率降低,因此固定的荧光团量较少。我们讨论MEF如何用于提高DNA阵列的敏感性,特别是对于CY5等远红色发射荧光团,而不是显着改变电流微阵列方案。

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