Peptide Binder with High-Affinity for the SARS-CoV-2 Spike Receptor-Binding Domain.
Rapid antigen detection tests are urgently needed for the early diagnosis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The discovery of a binder with high affinity and selectivity for the biomarkers presented by SARS-CoV-2 is crucial to the development of the rapid antigen detection method. We utilized the surface ... biopanning to identify a peptide binder R1 from a phage-displayed peptide library consisting of 109 independent phage recombinants. The R1 peptide exhibited high-affinity for specific binding with the receptor-binding domain (RBD) of the SARS-CoV-2 spike protein with a dissociation constant KD of (7.5 ± 1.9) × 10-10 M, which maintained high binding affinity with the RBD derived from Gamma, Lambda, Delta, and Omicron variants. The composition and sequence dependence of binding characteristics in R1-RBD interactions was revealed by the binding affinity fluctuations between RBD and the scrambled sequences or single-site mutants of R1. The R1-functionalized gold nanoparticles possessed concentration-dependent response to RBD and selectivity over bovine serum albumin and human serum albumin. The peptide binder R1 shows the potential to be used for constructing a rapid detection method for the early-stage diagnostics for SARS-CoV-2.
Mesh Terms:
Antibodies, Viral, Binding Sites, COVID-19, Gold, Humans, Metal Nanoparticles, Peptide Library, Protein Binding, SARS-CoV-2, Spike Glycoprotein, Coronavirus
Antibodies, Viral, Binding Sites, COVID-19, Gold, Humans, Metal Nanoparticles, Peptide Library, Protein Binding, SARS-CoV-2, Spike Glycoprotein, Coronavirus
ACS Appl Mater Interfaces
Date: Jun. 29, 2022
PubMed ID: 35713340
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