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用于即时 SARS-CoV-2 抗体检测的发光生物传感器的工程设计。

Engineering luminescent biosensors for point-of-care SARS-CoV-2 antibody detection.

机构信息

Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, USA.

Soteria Biotherapeutics, San Francisco, CA, USA.

出版信息

Nat Biotechnol. 2021 Aug;39(8):928-935. doi: 10.1038/s41587-021-00878-8. Epub 2021 Mar 25.

Abstract

Current serology tests for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies mainly take the form of enzyme-linked immunosorbent assays, chemiluminescent microparticle immunoassays or lateral flow assays, which are either laborious, expensive or lacking sufficient sensitivity and scalability. Here we present the development and validation of a rapid, low-cost, solution-based assay to detect antibodies in serum, plasma, whole blood and to a lesser extent saliva, using rationally designed split luciferase antibody biosensors. This new assay, which generates quantitative results in 30 min, substantially reduces the complexity and improves the scalability of coronavirus disease 2019 (COVID-19) antibody tests. This assay is well-suited for point-of-care, broad population testing, and applications in low-resource settings, for monitoring host humoral responses to vaccination or viral infection.

摘要

目前针对严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 抗体的血清学检测主要采用酶联免疫吸附测定法、化学发光微粒子免疫测定法或侧向流动测定法,这些方法要么繁琐、昂贵,要么缺乏足够的灵敏度和可扩展性。在这里,我们开发并验证了一种快速、低成本的基于溶液的检测方法,该方法使用经过合理设计的分裂荧光素酶抗体生物传感器来检测血清、血浆和全血中的抗体,在一定程度上还可以检测唾液中的抗体。这种新的检测方法在 30 分钟内即可产生定量结果,大大降低了复杂性,提高了 COVID-19 抗体检测的可扩展性。该检测方法非常适合于即时检测、大规模人群检测,以及在资源有限的环境中用于监测宿主对疫苗接种或病毒感染的体液免疫反应。

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