| Literature DB >> 33904225 |
Teresa R Wagner1,2, Elena Ostertag3, Philipp D Kaiser2, Marius Gramlich2, Natalia Ruetalo4, Daniel Junker2, Julia Haering2, Bjoern Traenkle2, Matthias Becker2, Alex Dulovic2, Helen Schweizer5, Stefan Nueske5, Armin Scholz5, Anne Zeck2, Katja Schenke-Layland2,6,7,8, Annika Nelde6,9,10, Monika Strengert11,12, Juliane S Walz6,9,10,13, Georg Zocher3, Thilo Stehle3,14, Michael Schindler4, Nicole Schneiderhan-Marra2, Ulrich Rothbauer1,2,6.
Abstract
In light of the COVID-19 pandemic, there is an ongoing need for diagnostic tools to monitor the immune status of large patient cohorts and the effectiveness of vaccination campaigns. Here, we present 11 unique nanobodies (Nbs) specific for the SARS-CoV-2 spike receptor-binding domain (RBD), of which 8 Nbs potently inhibit the interaction of RBD with angiotensin-converting enzyme 2 (ACE2) as the major viral docking site. Following detailed epitope mapping and structural analysis, we select two inhibitory Nbs, one of which binds an epitope inside and one of which binds an epitope outside the RBD:ACE2 interface. Based on these, we generate a biparatopic nanobody (bipNb) with viral neutralization efficacy in the picomolar range. Using bipNb as a surrogate, we establish a competitive multiplex binding assay ("NeutrobodyPlex") for detailed analysis of the presence and performance of neutralizing RBD-binding antibodies in serum of convalescent or vaccinated patients. We demonstrate that NeutrobodyPlex enables high-throughput screening and detailed analysis of neutralizing immune responses in infected or vaccinated individuals, to monitor immune status or to guide vaccine design. ©2021 The Authors. Published under the terms of the CC BY 4.0 license.Entities:
Keywords: SARS-CoV-2; immune response; nanobodies; neutralizing antibodies; serological assay
Year: 2021 PMID: 33904225 DOI: 10.15252/embr.202052325
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807