This is a preprint.
Rapid 'mix and read' assay for scalable detection of SARS-CoV-2 antibodies in patient plasma
- PMID: 32909004
- PMCID: PMC7480056
- DOI: 10.1101/2020.09.01.20184101
Rapid 'mix and read' assay for scalable detection of SARS-CoV-2 antibodies in patient plasma
Update in
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Diagnostic TR-FRET assays for detection of antibodies in patient samples.Cell Rep Methods. 2023 Feb 20;3(3):100421. doi: 10.1016/j.crmeth.2023.100421. eCollection 2023 Mar 27. Cell Rep Methods. 2023. PMID: 37056371 Free PMC article.
Abstract
The human beta coronavirus SARS-CoV-2, causative virus of COVID-19, has infected more than 15 million people globally and continues to spread. Widespread, population level testing to detect active and past infections is critical to curb the COVID-19 pandemic. Antibody (serological) testing is the only option for detecting past infections outside the narrow window accessible to nucleic acid-based tests. However, currently available serological assays commonly lack scalability. Here, we describe the development of a rapid homogenous serological assay for the detection of antibodies to SARS-CoV-2 in patient plasma. We show that the fluorescence-based assay accurately detects seroconversion in COVID-19 patients from less than 1 microliter of plasma. Using a cohort of samples from COVID-19 infected or healthy individuals, we demonstrate detection with 100% sensitivity and specificity. This assay addresses an important need for a robust, low barrier to implementation, and scalable serological assay with complementary strengths to currently available serological platforms.
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