Laboratory of Cell Technology, Department of Biotechnology, Agricultural University of Athens, EU-CONEXUS European University, 11855 Athens, Greece.
Sensors (Basel). 2020 May 31;20(11):3121. doi: 10.3390/s20113121.
One of the key challenges of the recent COVID-19 pandemic is the ability to accurately estimate the number of infected individuals, particularly asymptomatic and/or early-stage patients. We herewith report the proof-of-concept development of a biosensor able to detect the SARS-CoV-2 S1 spike protein expressed on the surface of the virus. The biosensor is based on membrane-engineered mammalian cells bearing the human chimeric spike S1 antibody. We demonstrate that the attachment of the protein to the membrane-bound antibodies resulted in a selective and considerable change in the cellular bioelectric properties measured by means of a Bioelectric Recognition Assay. The novel biosensor provided results in an ultra-rapid manner (3 min), with a detection limit of 1 fg/mL and a semi-linear range of response between 10 fg and 1 μg/mL. In addition, no cross-reactivity was observed against the SARS-CoV-2 nucleocapsid protein. Furthermore, the biosensor was configured as a ready-to-use platform, including a portable read-out device operated via smartphone/tablet. In this way, we demonstrate that the novel biosensor can be potentially applied for the mass screening of SARS-CoV-2 surface antigens without prior sample processing, therefore offering a possible solution for the timely monitoring and eventual control of the global coronavirus pandemic.
新冠疫情期间面临的主要挑战之一是能否准确估计受感染个体的数量,尤其是无症状和/或早期患者。在此,我们报告了一种能够检测病毒表面表达的 SARS-CoV-2 S1 刺突蛋白的生物传感器的概念验证开发。该生物传感器基于带有人类嵌合 Spike S1 抗体的工程化哺乳动物细胞的膜。我们证明,蛋白与膜结合抗体的附着导致通过生物电识别测定测量的细胞生物物理特性发生选择性和显著变化。新型生物传感器能够非常快速地(3 分钟)提供结果,检测限为 1 fg/mL,响应的半线性范围在 10 fg 和 1 μg/mL 之间。此外,未观察到针对 SARS-CoV-2 核衣壳蛋白的交叉反应性。此外,该生物传感器被配置为即插即用的平台,包括通过智能手机/平板电脑操作的便携式读出设备。通过这种方式,我们证明新型生物传感器可用于对 SARS-CoV-2 表面抗原进行大规模筛选,而无需进行样品预处理,因此为及时监测和最终控制全球冠状病毒大流行提供了一种可能的解决方案。