Robert F. Smith School of Chemical and Biomolecular Engineering, Cornell University, Olin Hall, Ithaca, New York 14853, United States.
Department of Chemical Engineering and Biotechnology, University of Cambridge, Philippa Fawcett Drive, CB30AS Cambridge, United Kingdom.
ACS Nano. 2021 Nov 23;15(11):18142-18152. doi: 10.1021/acsnano.1c06813. Epub 2021 Oct 25.
Emerging viruses will continue to be a threat to human health and wellbeing into the foreseeable future. The COVID-19 pandemic revealed the necessity for rapid viral sensing and inhibitor screening in mitigating viral spread and impact. Here, we present a platform that uses a label-free electronic readout as well as a dual capability of optical (fluorescence) readout to sense the ability of a virus to bind and fuse with a host cell membrane, thereby sensing viral entry. This approach introduces a hitherto unseen level of specificity by distinguishing fusion-competent viruses from fusion-incompetent viruses. The ability to discern between competent and incompetent viruses means that this device could also be used for applications beyond detection, such as screening antiviral compounds for their ability to block virus entry mechanisms. Using optical means, we first demonstrate the ability to recapitulate the entry processes of influenza virus using a biomembrane containing the viral receptor that has been functionalized on a transparent organic bioelectronic device. Next, we detect virus membrane fusion, using the same, label-free devices. Using both reconstituted and native cell membranes as materials to functionalize organic bioelectronic devices, configured as electrodes and transistors, we measure changes in membrane properties when virus fusion is triggered by a pH drop, inducing hemagglutinin to undergo a conformational change that leads to membrane fusion.
未来可预见,新出现的病毒将继续对人类健康和福祉构成威胁。COVID-19 大流行揭示了在减轻病毒传播和影响方面快速进行病毒检测和抑制剂筛选的必要性。在这里,我们提出了一个使用无标记电子读出以及光学(荧光)读出双重功能来感测病毒与宿主细胞膜结合和融合从而感测病毒进入的平台。这种方法通过区分融合能力病毒和融合能力不足的病毒,引入了前所未有的特异性水平。区分有能力和无能力的病毒的能力意味着该设备也可用于除检测之外的应用,例如筛选抗病毒化合物阻断病毒进入机制的能力。我们首先使用含有已在透明有机生物电子设备上功能化的病毒受体的生物膜,通过光学手段来首次演示模拟流感病毒进入过程的能力。接下来,我们使用相同的无标记设备检测病毒膜融合。我们使用重组和天然细胞膜作为功能化有机生物电子设备的材料,将其配置为电极和晶体管,当 pH 值下降引发血凝素发生构象变化导致膜融合时,我们测量膜特性的变化,从而触发病毒融合。