A surrogate cell‐based SARS‐CoV‐2 spike blocking assay

Abstract: To monitor infection by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and successful vaccination against coronavirus disease 2019 (COVID-19), the kinetics of neutralizing or blocking anti-SARS-CoV-2 antibody titers need to be assessed. Here, we report the development of a quick and inexpensive surrogate SARS-CoV-2 blocking assay (SUBA) using immobilized recombinant human angiotensin-converting enzyme 2 (hACE2) and human cells expressing the native form of surface SARS-CoV-2 spike protein. Spike protein-expressing cells bound to hACE2 in the absence or presence of blocking antibodies were quantified by measuring the optical density of cell-associated crystal violet in a spectrophotometer. The advantages are that SUBA is a fast and inexpensive assay, which does not require biosafety level 2- or 3-approved laboratories. Most importantly, SUBA detects blocking antibodies against the native trimeric cell-bound SARS-CoV-2 spike protein and can be rapidly adjusted to quickly pre-screen already approved therapeutic antibodies or sera from vaccinated individuals for their ACE2 blocking activities against any emerging SARS-CoV-2 variants

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
European journal of immunology. - 51, 11 (2021) , 2665-2676, ISSN: 1521-4141

Classification
Medizin, Gesundheit

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2024
Creator
Schuh, Wolfgang
Baus, Lena
Steinmetz, Tobit
Schulz, Sebastian R.
Weckwerth, Leonie
Roth, Edith
Hauke, Manuela
Krause, Sara
Morhart, Patrick Daniel
Rauh, Manfred
Hoffmann, Markus
Vesper, Niklas
Reth, Michael
Schneider, Holm
Jäck, Hans-Martin
Mielenz, Dirk Alexander

DOI
10.1002/eji.202149302
URN
urn:nbn:de:bsz:25-freidok-2482323
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.2025, 1:54 PM CET

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Associated

Time of origin

  • 2024

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