학술논문

Bi-paratopic and multivalent VH domains block ACE2 binding and neutralize SARS-CoV-2
Document Type
article
Source
Nature Chemical Biology. 17(1)
Subject
Biological Sciences
Bioinformatics and Computational Biology
Biodefense
Vaccine Related
Clinical Research
Prevention
Lung
Emerging Infectious Diseases
Infectious Diseases
Pneumonia & Influenza
Pneumonia
Development of treatments and therapeutic interventions
5.1 Pharmaceuticals
Good Health and Well Being
Angiotensin-Converting Enzyme 2
Animals
Antibodies
Neutralizing
Antibodies
Viral
Binding Sites
Antibody
Chlorocebus aethiops
Cryoelectron Microscopy
HEK293 Cells
Humans
Models
Molecular
Peptide Library
Protein Binding
Protein Conformation
alpha-Helical
Protein Conformation
beta-Strand
Protein Interaction Domains and Motifs
SARS-CoV-2
Single-Chain Antibodies
Spike Glycoprotein
Coronavirus
Vero Cells
QCRG Structural Biology Consortium
Medicinal and Biomolecular Chemistry
Biochemistry and Cell Biology
Biochemistry & Molecular Biology
Biochemistry and cell biology
Medicinal and biomolecular chemistry
Language
Abstract
Neutralizing agents against SARS-CoV-2 are urgently needed for the treatment and prophylaxis of COVID-19. Here, we present a strategy to rapidly identify and assemble synthetic human variable heavy (VH) domains toward neutralizing epitopes. We constructed a VH-phage library and targeted the angiotensin-converting enzyme 2 (ACE2) binding interface of the SARS-CoV-2 Spike receptor-binding domain (Spike-RBD). Using a masked selection approach, we identified VH binders to two non-overlapping epitopes and further assembled these into multivalent and bi-paratopic formats. These VH constructs showed increased affinity to Spike (up to 600-fold) and neutralization potency (up to 1,400-fold) on pseudotyped SARS-CoV-2 virus when compared to standalone VH domains. The most potent binder, a trivalent VH, neutralized authentic SARS-CoV-2 with a half-maximal inhibitory concentration (IC50) of 4.0 nM (180 ng ml-1). A cryo-EM structure of the trivalent VH bound to Spike shows each VH domain engaging an RBD at the ACE2 binding site, confirming our original design strategy.