Laboratory of Protein Engineering, Department of Biomedical Engineering and Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven 5600 MB, The Netherlands.
Department of Chemistry and Pharmaceutical Sciences, Amsterdam Institute of Molecular and Life Sciences, Vrije Universiteit Amsterdam, Amsterdam 1081 HZ, The Netherlands.
ACS Sens. 2024 Oct 25;9(10):5550-5560. doi: 10.1021/acssensors.4c01855. Epub 2024 Oct 7.
Respiratory viruses such as SARS-CoV-2, influenza, and respiratory syncytial virus (RSV) represent pressing health risks. Rapid diagnostic tests for these viruses detect single antigens or nucleic acids, which do not necessarily correlate with the amount of the intact virus. Instead, specific detection of intact respiratory virus particles may be more effective at assessing the contagiousness of a patient. Here, we report GLOVID, a modular biosensor platform to detect intact virions against a background of "free" viral proteins in solution. Our approach harnesses the multivalent display of distinct proteins on the surface of a viral particle to template the reconstitution of a split luciferase, allowing specific, single-step detection of intact influenza A and RSV virions corresponding to 0.1-0.3 fM of genomic units. The protein ligation system used to assemble GLOVID sensors is compatible with a broad range of binding domains, including nanobodies, scFv fragments, and cyclic peptides, which allows straightforward adjustment of the sensor platform to target different viruses.
呼吸道病毒,如严重急性呼吸综合征冠状病毒 2 型(SARS-CoV-2)、流感病毒和呼吸道合胞病毒(RSV),是紧迫的健康威胁。这些病毒的快速诊断检测方法可检测单一抗原或核酸,这些并不一定与完整病毒的数量相关。相反,对完整呼吸道病毒颗粒的特异性检测可能更有效地评估患者的传染性。在这里,我们报告了 GLOVID,这是一种模块化生物传感器平台,用于在溶液中“游离”病毒蛋白的背景下检测完整病毒粒子。我们的方法利用病毒粒子表面上不同蛋白质的多价展示来模板化分裂萤光素酶的重组,从而可以特异性、一步检测到对应于 0.1-0.3 fM 基因组单位的完整流感 A 和 RSV 病毒粒子。用于组装 GLOVID 传感器的蛋白连接系统与广泛的结合结构域兼容,包括纳米抗体、scFv 片段和环状肽,这使得可以轻松调整传感器平台以针对不同的病毒。