Department of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
Nick Holonyak Jr. Micro and Nanotechnology Laboratory, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
J Am Chem Soc. 2022 Feb 2;144(4):1498-1502. doi: 10.1021/jacs.1c09579. Epub 2021 Dec 20.
Several applications in health diagnostics, food, safety, and environmental monitoring require rapid, simple, selective, and quantitatively accurate viral load monitoring. Here, we introduce the first label-free biosensing method that rapidly detects and quantifies intact virus in human saliva with single-virion resolution. Using pseudotype SARS-CoV-2 as a representative target, we immobilize aptamers with the ability to differentiate active from inactive virions on a photonic crystal, where the virions are captured through affinity with the spike protein displayed on the outer surface. Once captured, the intrinsic scattering of the virions is amplified and detected through interferometric imaging. Our approach analyzes the motion trajectory of each captured virion, enabling highly selective recognition against nontarget virions, while providing a limit of detection of 1 × 10 copies/mL at room temperature. The approach offers an alternative to enzymatic amplification assays for point-of-collection diagnostics.
在健康诊断、食品、安全和环境监测等多个领域,人们需要快速、简便、选择性强且定量准确的病毒载量监测方法。在此,我们介绍了首个无需标记的生物传感方法,该方法可实现单病毒分辨率下对人唾液中完整病毒的快速检测和定量。我们以假型 SARS-CoV-2 作为代表性靶标,将具有区分活性和非活性病毒能力的适体固定在光子晶体上,通过与病毒外表面展示的刺突蛋白的亲和力,病毒被捕获。一旦被捕获,病毒的固有散射就会被放大,并通过干涉成像进行检测。我们的方法分析每个捕获病毒的运动轨迹,从而能够针对非靶标病毒进行高度选择性识别,同时在室温下实现 1×10 拷贝/mL 的检测限。该方法为现场采集诊断提供了一种替代酶扩增检测的方法。