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Development of Monoclonal Antibodies to Detect for SARS-CoV-2 Proteins

机译:开发用于检测 SARS-CoV-2 蛋白的单克隆抗体

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摘要

The COVID-19 pandemic caused by SARS-CoV-2 infection has impacted the world economy and healthcare infrastructure. Key reagents with high specificity to SARS-CoV-2 proteins are currently lacking, which limits our ability to understand the pathophysiology of SARS-CoV-2 infections. To address this need, we initiated a series of studies to generate and develop highly specific antibodies against proteins from SARS-CoV-2 using an antibody engineering platform. These efforts resulted in 18 monoclonal antibodies against nine SARS-CoV-2 proteins. Here we report the characterization of several antibodies, including those that recognize Nsp1, Nsp8, Nsp12, and Orf3b viral proteins. Our validation studies included evaluation for use of antibodies in ELISA, western blots, and immunofluorescence assays (IFA). We expect that availability of these antibodies will enhance our ability to further characterize host-viral interactions, including specific roles played by viral proteins during infection, to acquire a better understanding of the pathophysiology of SARS-CoV-2 infections. (C) 2022 Published by Elsevier Ltd.
机译:由 SARS-CoV-2 感染引起的 COVID-19 大流行影响了世界经济和医疗保健基础设施。目前缺乏对 SARS-CoV-2 蛋白具有高度特异性的关键试剂,这限制了我们了解 SARS-CoV-2 感染病理生理学的能力。为了满足这一需求,我们启动了一系列研究,以使用抗体工程平台生成和开发针对 SARS-CoV-2 蛋白质的高特异性抗体。这些努力产生了针对 9 种 SARS-CoV-2 蛋白的 18 种单克隆抗体。在这里,我们报告了几种抗体的表征,包括识别 Nsp1、Nsp8、Nsp12 和 Orf3b 病毒蛋白的抗体。我们的验证研究包括评估抗体在ELISA中的应用、蛋白质印迹和免疫荧光测定(IFA)。我们预计这些抗体的可用性将增强我们进一步表征宿主-病毒相互作用的能力,包括病毒蛋白在感染过程中发挥的特定作用,从而更好地了解 SARS-CoV-2 感染的病理生理学。(C) 2022年由Elsevier Ltd.出版。

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