Microfluidic Diffusional Sizing (MDS) Measurements of Secretory Neutralizing Antibody Affinity Against SARS-CoV-2

SARS-CoV-2 has rampantly spread around the globe and continues to cause unprecedented loss through ongoing waves of (re)infection. Increasing our understanding of the protection against infection with SARS-CoV-2 is critical to ending the pandemic. Serological assays have been widely used to assess i...

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Veröffentlicht in:Annals of biomedical engineering 2024-06, Vol.52 (6), p.1653-1664
Hauptverfasser: O’Mahoney, Cara, Watt, Ian, Fiedler, Sebastian, Devenish, Sean, Srikanth, Sujata, Justice, Erica, Dover, Tristan, Dean, Delphine, Peng, Congyue
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container_end_page 1664
container_issue 6
container_start_page 1653
container_title Annals of biomedical engineering
container_volume 52
creator O’Mahoney, Cara
Watt, Ian
Fiedler, Sebastian
Devenish, Sean
Srikanth, Sujata
Justice, Erica
Dover, Tristan
Dean, Delphine
Peng, Congyue
description SARS-CoV-2 has rampantly spread around the globe and continues to cause unprecedented loss through ongoing waves of (re)infection. Increasing our understanding of the protection against infection with SARS-CoV-2 is critical to ending the pandemic. Serological assays have been widely used to assess immune responses, but secretory antibodies, the essential first line of defense, have been studied to only a limited extent. Of particular interest and importance are neutralizing antibodies, which block the binding of the spike protein of SARS-CoV-2 to the human receptor angiotensin-converting enzyme-2 (ACE2) and thus are essential for immune defense. Here, we employed Microfluidic Diffusional Sizing (MDS), an immobilization-free technology, to characterize neutralizing antibody affinity to SARS-CoV-2 spike receptor-binding domain (RBD) and spike trimer in saliva. Affinity measurement was obtained through a contrived sample and buffer using recombinant SARS-CoV-2 RBD and monoclonal antibody. Limited saliva samples demonstrated that MDS applies to saliva neutralizing antibody measurement. The ability to disrupt a complex of ACE2-Fc and spike trimer is shown. Using a quantitative assay on the patient sample, we determined the affinity and binding site concentration of the neutralizing antibodies.
doi_str_mv 10.1007/s10439-024-03478-0
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subjects ACE2
Affinity
Angiotensin
Angiotensin-converting enzyme 2
Antibodies
Binding sites
Biochemistry
Biological and Medical Physics
Biomedical and Life Sciences
Biomedical Engineering and Bioengineering
Biomedicine
Biophysics
Classical Mechanics
COVID-19
Immobilization
Immune response
Immune system
Microfluidics
Monoclonal antibodies
Neutralizing
Original Article
Pandemics
Peptidyl-dipeptidase A
Receptors
Saliva
Severe acute respiratory syndrome coronavirus 2
Sizing
Spike protein
Trimers
Viral diseases
title Microfluidic Diffusional Sizing (MDS) Measurements of Secretory Neutralizing Antibody Affinity Against SARS-CoV-2
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