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Spatially selective photonic crystal enhanced fluorescence and application to background reduction for biomolecule detection assays

机译:空间选择性光子晶体增强了荧光并应用于生物分子检测测定的背景降低

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摘要

By combining photonic crystal label-free biosensor imaging with photonic crystal enhanced fluorescence, it is possible to selectively enhance the fluorescence emission from regions of the PC surface based upon the density of immobilized capture molecules. A label-free image of the capture molecules enables determination of optimal coupling conditions of the laser used for fluorescence imaging of the photonic crystal surface on a pixel-by-pixel basis, allowing maximization of fluorescence enhancement factor from regions incorporating a biomolecule capture spot and minimization of background autofluorescence from areas between capture spots. This capability significantly improves the contrast of enhanced fluorescent images, and when applied to an antibody protein microarray, provides a substantial advantage over conventional fluorescence microscopy. Using the new approach, we demonstrate detection limits as low as 0.97 pg/ml for a representative protein biomarker in buffer.
机译:通过将无光子晶体标记的生物传感器成像与光子晶体增强的荧光相结合,可以根据固定的捕获分子的密度选择性地增强PC表面区域的荧光发射。捕获分子的无标记图像能够确定逐个像素地对光子晶体表面进行荧光成像的激光的最佳耦合条件,从而使包含生物分子捕获点的区域的荧光增强因子最大化。最小化捕获点之间区域的背景自发荧光。此功能显着改善了增强的荧光图像的对比度,并且当应用于抗体蛋白质微阵列时,与常规的荧光显微镜相比具有明显的优势。使用新方法,我们证明了缓冲液中代表性蛋白质生物标志物的检测限低至0.97 pg / ml。

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