Institut Pasteur de Montevideo, Montevideo, Uruguay.
Laboratory of Molecular and Cellular Virology, Virology Program, Institute of Biomedical Sciences, Faculty of Medicine, Universidad de Chile, Santiago, Chile.
Front Immunol. 2023 Aug 10;14:1226880. doi: 10.3389/fimmu.2023.1226880. eCollection 2023.
The COVID-19 pandemic evolves constantly, requiring adaptable solutions to combat emerging SARS-CoV-2 variants. To address this, we created a pentameric scaffold based on a mammalian protein, which can be customized with up to 10 protein binding modules. This molecular scaffold spans roughly 20 nm and can simultaneously neutralize SARS-CoV-2 Spike proteins from one or multiple viral particles. Using only two different modules targeting the Spike's RBD domain, this construct outcompetes human antibodies from vaccinated individuals' serum and blocks cell attachment and pseudotyped virus entry. Additionally, the multibodies inhibit viral replication at low picomolar concentrations, regardless of the variant. This customizable multibody can be easily produced in procaryote systems, providing a new avenue for therapeutic development and detection devices, and contributing to preparedness against rapidly evolving pathogens.
COVID-19 大流行不断演变,需要适应性解决方案来应对新出现的 SARS-CoV-2 变体。为此,我们创建了一个基于哺乳动物蛋白的五聚体支架,该支架可以用多达 10 个蛋白结合模块进行定制。这种分子支架跨度约 20nm,可以同时中和来自一个或多个病毒颗粒的 SARS-CoV-2 刺突蛋白。仅使用两个针对 Spike 的 RBD 结构域的不同模块,该构建体即可与来自接种疫苗个体血清的人抗体竞争,并阻止细胞附着和假型病毒进入。此外,多抗体以低皮摩尔浓度抑制病毒复制,无论变体如何。这种可定制的多抗体可以在原核系统中轻松生产,为治疗开发和检测设备提供了新途径,并有助于防范快速进化的病原体。