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Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition.

Publication ,  Journal Article
Kramer, KJ; Johnson, NV; Shiakolas, AR; Suryadevara, N; Periasamy, S; Raju, N; Williams, JK; Wrapp, D; Zost, SJ; Walker, LM; Wall, SC ...
Published in: Cell Rep
October 5, 2021

The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) lineages that are more transmissible and resistant to currently approved antibody therapies poses a considerable challenge to the clinical treatment of coronavirus disease (COVID-19). Therefore, the need for ongoing discovery efforts to identify broadly reactive monoclonal antibodies to SARS-CoV-2 is of utmost importance. Here, we report a panel of SARS-CoV-2 antibodies isolated using the linking B cell receptor to antigen specificity through sequencing (LIBRA-seq) technology from an individual who recovered from COVID-19. Of these antibodies, 54042-4 shows potent neutralization against authentic SARS-CoV-2 viruses, including variants of concern (VOCs). A cryoelectron microscopy (cryo-EM) structure of 54042-4 in complex with the SARS-CoV-2 spike reveals an epitope composed of residues that are highly conserved in currently circulating SARS-CoV-2 lineages. Further, 54042-4 possesses uncommon genetic and structural characteristics that distinguish it from other potently neutralizing SARS-CoV-2 antibodies. Together, these findings provide motivation for the development of 54042-4 as a lead candidate to counteract current and future SARS-CoV-2 VOCs.

Duke Scholars

Published In

Cell Rep

DOI

EISSN

2211-1247

Publication Date

October 5, 2021

Volume

37

Issue

1

Start / End Page

109784

Location

United States

Related Subject Headings

  • Vero Cells
  • Spike Glycoprotein, Coronavirus
  • SARS-CoV-2
  • Receptors, Antigen, B-Cell
  • Protein Interaction Domains and Motifs
  • Protein Binding
  • Middle Aged
  • Male
  • Humans
  • High-Throughput Screening Assays
 

Citation

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Kramer, K. J., Johnson, N. V., Shiakolas, A. R., Suryadevara, N., Periasamy, S., Raju, N., … Georgiev, I. S. (2021). Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition. Cell Rep, 37(1), 109784. https://doi.org/10.1016/j.celrep.2021.109784
Kramer, Kevin J., Nicole V. Johnson, Andrea R. Shiakolas, Naveenchandra Suryadevara, Sivakumar Periasamy, Nagarajan Raju, Jazmean K. Williams, et al. “Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition.Cell Rep 37, no. 1 (October 5, 2021): 109784. https://doi.org/10.1016/j.celrep.2021.109784.
Kramer KJ, Johnson NV, Shiakolas AR, Suryadevara N, Periasamy S, Raju N, et al. Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition. Cell Rep. 2021 Oct 5;37(1):109784.
Kramer, Kevin J., et al. “Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition.Cell Rep, vol. 37, no. 1, Oct. 2021, p. 109784. Pubmed, doi:10.1016/j.celrep.2021.109784.
Kramer KJ, Johnson NV, Shiakolas AR, Suryadevara N, Periasamy S, Raju N, Williams JK, Wrapp D, Zost SJ, Walker LM, Wall SC, Holt CM, Hsieh C-L, Sutton RE, Paulo A, Nargi RS, Davidson E, Doranz BJ, Crowe JE, Bukreyev A, Carnahan RH, McLellan JS, Georgiev IS. Potent neutralization of SARS-CoV-2 variants of concern by an antibody with an uncommon genetic signature and structural mode of spike recognition. Cell Rep. 2021 Oct 5;37(1):109784.
Journal cover image

Published In

Cell Rep

DOI

EISSN

2211-1247

Publication Date

October 5, 2021

Volume

37

Issue

1

Start / End Page

109784

Location

United States

Related Subject Headings

  • Vero Cells
  • Spike Glycoprotein, Coronavirus
  • SARS-CoV-2
  • Receptors, Antigen, B-Cell
  • Protein Interaction Domains and Motifs
  • Protein Binding
  • Middle Aged
  • Male
  • Humans
  • High-Throughput Screening Assays