Microfluidic Diffusional Sizing (MDS) Measurements of Secretory Neutralizing Antibody Affinity Against SARS-CoV-2.
Cara O'MahoneyIan WattSebastian FiedlerSean DevenishSujata SrikanthErica JusticeTristan DoverDelphine DeanCongyue Annie PengPublished in: Annals of biomedical engineering (2024)
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.
Keyphrases
- sars cov
- angiotensin converting enzyme
- respiratory syndrome coronavirus
- dengue virus
- angiotensin ii
- high throughput
- immune response
- monoclonal antibody
- binding protein
- single cell
- endothelial cells
- circulating tumor cells
- capillary electrophoresis
- zika virus
- inflammatory response
- dna binding
- dendritic cells
- label free