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Planar Waveguides as High-Performance Sensing Platforms for Fluorescence-Based Multiplexed Oligonucleotide Hybridization Assays

机译:平面波导作为基于荧光的多重寡核苷酸杂交检测的高性能传感平台

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摘要

16-Mer and 22-mer oligonucleotide capture probes with an amino function at the 5'-end were covalently immobilized on (3-glycidoxypropyl)trimethoxysilane (GOPTS) silanized planar waveguides in “checkerboard”-style 2-dimensional arrays by means of ink-jet printing in order to demonstrate the potential of multiplexed planar waveguide biosensing. The laser-induced fluorescence was collected by a CCD camera, providing quantitative information regarding the intensity of individual sensing pads. In model hybridization assays with Cy5-labeled complementary oligonucleotides, sample concentrations down to 50 fM were successfully detected within 12 min. The overall spot-to-spot variability of the ink-jet immobilization in combination with amino functionalized oligonucleofides and GOPTS silanized waveguides was found to be about 12% and almost independent of the formation of an equllibrium between the labeled analyte and capture probes. Both pipet-made and ink-jet-made oligonucleotide spots showed comparable assay performances.
机译:在5'端具有氨基功能的16-mer和22-mer寡核苷酸捕获探针通过墨水共价固定在“棋盘”式二维阵列中的(3-环氧丙氧基丙基)三甲氧基硅烷(GOPTS)硅烷化的平面波导上喷射印刷,以证明多重平面波导生物传感的潜力。激光诱导的荧光由CCD相机收集,可提供有关各个感应垫强度的定量信息。在用Cy5标记的互补寡核苷酸进行的模型杂交测定中,成功在12分钟内检测到低至50 fM的样品浓度。发现与氨基官能化的寡核苷酸和GOPTS硅烷化的波导相结合,喷墨固定的整体点对点变异性约为12%,并且几乎与标记的分析物和捕获探针之间平衡的形成无关。移液制备的和喷墨制备的寡核苷酸斑点均显示出相当的测定性能。

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