Lee Nuree, Wang Cong, Park Jungyul
Department of Mechanical Engineering, Sogang University 35 Baekbeom-ro (Shinsu-dong), Mapo-gu Seoul 04107 Korea
Interdisciplinary Program of Integrated Biotechnology, Sogang University 35 Baekbeom-ro (Shinsu-dong), Mapo-gu Seoul 04107 Korea.
RSC Adv. 2018 Jun 22;8(41):22991-22997. doi: 10.1039/c8ra02596g. eCollection 2018 Jun 21.
This paper proposes a user-friendly and highly sensitive detection method for influenza A (H1N1) virus using the cooperation of quantum dot (Qdot)-aptamer beacons and light guide in a three-dimensional (3D) photonic crystal (PC). For easy use, we present a fluorescent probe-based 'OFF-ON' detection protocol. First, a mixture composed of Qdot-aptamer beacons and dark quencher-labeled guard DNA (G-DNA) was prepared. It initially quenched the fluorescent signals to significantly low intensity, , 'OFF' state. Then, the influenza A (H1N1) virus preferentially bound to the aptamer and G-DNA was released, so that the fluorescent signal was restored and biosensor turned to 'ON' state. The restored fluorescence signal changed quantitatively according to the concentration of the target influenza A (H1N1) virus. Owing to the light guide of the 3D nanoporous PC structure, we achieved high sensitivity with ultra-low limit of detection (LOD) of 138 pg mL and high selectivity over other species of influenza A virus and biomolecules. Additionally, with the benefit of enhanced output fluorescent signals, the target virus could be easily detected with a low-cost and portable home-made setup (total cost of only 20 US dollars) and a built-in camera in a smartphone.
本文提出了一种利用量子点(Qdot)适配体信标与三维(3D)光子晶体(PC)中的光导相结合的方法,用于甲型流感(H1N1)病毒的用户友好型高灵敏度检测。为便于使用,我们提出了一种基于荧光探针的“关-开”检测方案。首先,制备了由Qdot适配体信标和暗猝灭剂标记的保护DNA(G-DNA)组成的混合物。它最初将荧光信号猝灭至极低强度,即“关”状态。然后,甲型流感(H1N1)病毒优先与适配体结合,G-DNA被释放,从而荧光信号恢复,生物传感器转变为“开”状态。恢复的荧光信号根据目标甲型流感(H1N1)病毒的浓度进行定量变化。由于3D纳米多孔PC结构的光导作用,我们实现了高灵敏度,检测限低至138 pg/mL,对其他甲型流感病毒和生物分子具有高选择性。此外,得益于增强的输出荧光信号,使用低成本的便携式自制装置(总成本仅20美元)和智能手机中的内置摄像头即可轻松检测目标病毒。