SUMMARY
Antibodies with heavy chains that derive from the VH1-2 gene constitute some of the most potent SARS-CoV-2-neutralizing antibodies yet identified. To provide insight into whether these genetic similarities inform common modes of recognition, we determined structures of the SARS-CoV-2 spike in complex with three VH1-2-derived antibodies: 2-15, 2-43, and H4. All three utilized VH1-2-encoded motifs to recognize the receptor-binding domain (RBD), with heavy chain N53I enhancing binding and light chain tyrosines recognizing F486RBD. Despite these similarities, class members bound both RBD-up and -down conformations of the spike, with a subset of antibodies utilizing elongated CDRH3s to recognize glycan N343 on a neighboring RBD – a quaternary interaction accommodated by an increase in RBD separation of up to 12 Å. The VH1-2-antibody class thus utilizes modular recognition encoded by modular genetic elements to effect potent neutralization, with VH-gene component specifying recognition of RBD and CDRH3 component specifying quaternary interactions.
Highlights
Determine structures of VH1-2-derived antibodies 2-43, 2-15, and H4 in complex with SARS-CoV-2 spike
Define a multi-donor VH1-2-antibody class with modular components for RBD and quaternary recognition
Reveal structural basis of RBD-up and RBD-down recognition within the class
Show somatic hypermutations and avidity to be critical for potency
Delineate changes in spike conformation induced by CDRH3-mediated quaternary recognition
Competing Interest Statement
DDH, YH, JY, LL, MSN and PW are inventors of a patent describing antibodies 2-43, 2-4, and 2-15 reported on here.
