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一种基于高通量纳米BiT的血清学检测方法可检测新型冠状病毒2型(SARS-CoV-2)血清转化。

A High-Throughput NanoBiT-Based Serological Assay Detects SARS-CoV-2 Seroconversion.

作者信息

Azad Taha, Rezaei Reza, Singaravelu Ragunath, Jamieson Taylor R, Crupi Mathieu J F, Surendran Abera, Poutou Joanna, Taklifi Parisa, Cowan Juthaporn, Cameron Donald William, Ilkow Carolina S

机构信息

Ottawa Hospital Research Institute, Ottawa, ON K1H 8L6, Canada.

Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, ON K1H 8M5, Canada.

出版信息

Nanomaterials (Basel). 2021 Mar 22;11(3):807. doi: 10.3390/nano11030807.

Abstract

High-throughput detection strategies for antibodies against SARS-CoV-2 in patients recovering from COVID-19, or in vaccinated individuals, are urgently required during this ongoing pandemic. Serological assays are the most widely used method to measure antibody responses in patients. However, most of the current methods lack the speed, stability, sensitivity, and specificity to be selected as a test for worldwide serosurveys. Here, we demonstrate a novel NanoBiT-based serological assay for fast and sensitive detection of SARS-CoV-2 RBD-specific antibodies in sera of COVID-19 patients. This assay can be done in high-throughput manner at 384 samples per hour and only requires a minimum of 5 μL of serum or 10 ng of antibody. The stability of our NanoBiT reporter in various temperatures (4-42 °C) and pH (4-12) settings suggests the assay will be able to withstand imperfect shipping and handling conditions for worldwide seroepidemiologic surveillance in the post-vaccination period of the pandemic. Our newly developed rapid assay is highly accessible and may facilitate a more cost-effective solution for seroconversion screening as vaccination efforts progress.

摘要

在这场仍在持续的大流行期间,迫切需要针对从新冠肺炎康复的患者或接种疫苗的个体中抗SARS-CoV-2抗体的高通量检测策略。血清学检测是测量患者抗体反应最广泛使用的方法。然而,目前大多数方法缺乏作为全球血清学调查检测方法所需的速度、稳定性、灵敏度和特异性。在此,我们展示了一种基于新型NanoBiT的血清学检测方法,用于快速、灵敏地检测新冠肺炎患者血清中SARS-CoV-2 RBD特异性抗体。该检测方法可以以每小时384个样本的高通量方式进行,并且仅需要最少5 μL血清或10 ng抗体。我们的NanoBiT报告基因在各种温度(4-42°C)和pH(4-12)设置下的稳定性表明,在大流行后的疫苗接种阶段,该检测方法将能够承受全球血清流行病学监测中不完善的运输和处理条件。我们新开发的快速检测方法易于使用,随着疫苗接种工作的推进,可能有助于为血清转化筛查提供更具成本效益的解决方案。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/266a/8004173/547004d3d909/nanomaterials-11-00807-g001.jpg

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