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空间选择性光子晶体增强荧光及其在生物分子检测分析背景降低中的应用。

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

作者信息

Chaudhery Vikram, Huang Cheng-Sheng, Pokhriyal Anusha, Polans James, Cunningham Brian T

机构信息

Dept. of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA.

出版信息

Opt Express. 2011 Nov 7;19(23):23327-40. doi: 10.1364/OE.19.023327.

Abstract

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.

摘要

通过将无标记光子晶体生物传感器成像与光子晶体增强荧光相结合,基于固定化捕获分子的密度,有可能选择性地增强光子晶体表面区域的荧光发射。捕获分子的无标记图像能够逐像素确定用于光子晶体表面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,使捕获点之间区域的背景自发荧光最小化。这种能力显著提高了增强荧光图像的对比度,当应用于抗体蛋白微阵列时,相对于传统荧光显微镜具有显著优势。使用这种新方法,我们证明了在缓冲液中对代表性蛋白质生物标志物的检测限低至0.97 pg/ml。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a27/3482899/577f80024f7c/oe-19-23-23327-g001.jpg

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