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利用共振介电纳米结构的共光路干涉无标记蛋白质传感

Common-path interferometric label-free protein sensing with resonant dielectric nanostructures.

作者信息

Barth Isabel, Conteduca Donato, Reardon Christopher, Johnson Steven, Krauss Thomas F

机构信息

Department of Physics, University of York, YO10 5DD York, UK.

Department of Electronic Engineering, University of York, YO10 5DD York, UK.

出版信息

Light Sci Appl. 2020 Jun 2;9:96. doi: 10.1038/s41377-020-0336-6. eCollection 2020.

Abstract

Research toward photonic biosensors for point-of-care applications and personalized medicine is driven by the need for high-sensitivity, low-cost, and reliable technology. Among the most sensitive modalities, interferometry offers particularly high performance, but typically lacks the required operational simplicity and robustness. Here, we introduce a common-path interferometric sensor based on guided-mode resonances to combine high performance with inherent stability. The sensor exploits the simultaneous excitation of two orthogonally polarized modes, and detects the relative phase change caused by biomolecular binding on the sensor surface. The wide dynamic range of the sensor, which is essential for fabrication and angle tolerance, as well as versatility, is controlled by integrating multiple, tuned structures in the field of view. This approach circumvents the trade-off between sensitivity and dynamic range, typical of other phase-sensitive modalities, without increasing complexity. Our sensor enables the challenging label-free detection of procalcitonin, a small protein (13 kDa) and biomarker for infection, at the clinically relevant concentration of 1 pg mL, with a signal-to-noise ratio of 35. This result indicates the utility for an exemplary application in antibiotic guidance, and opens possibilities for detecting further clinically or environmentally relevant small molecules with an intrinsically simple and robust sensing modality.

摘要

面向即时护理应用和个性化医疗的光子生物传感器的研究,是由对高灵敏度、低成本和可靠技术的需求所推动的。在最灵敏的检测方式中,干涉测量法具有特别高的性能,但通常缺乏所需的操作简便性和稳健性。在此,我们介绍一种基于导模共振的共光路干涉传感器,以将高性能与固有稳定性相结合。该传感器利用同时激发两个正交偏振模式,并检测由生物分子在传感器表面结合引起的相对相位变化。传感器的宽动态范围对于制造和角度容差以及通用性至关重要,它通过在视场中集成多个调谐结构来控制。这种方法避免了其他相敏检测方式典型的灵敏度和动态范围之间的权衡,而不会增加复杂性。我们的传感器能够在1 pg/mL的临床相关浓度下,以35的信噪比实现对降钙素原(一种13 kDa的小蛋白质和感染生物标志物)具有挑战性的无标记检测。这一结果表明了其在抗生素指导中的示例性应用效用,并为利用本质上简单且稳健的传感方式检测更多临床或环境相关小分子开辟了可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b56e/7265378/158d64b8f504/41377_2020_336_Fig1_HTML.jpg

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