AR222, AR249, AS274, AS702 and AS708 antibodies recognize the spike S protein from SARS-CoV-2 by ELISA

Authors

  • Philippe Hammel
  • Anna Marchetti
  • Frederic Zenhausern

DOI:

https://doi.org/10.24450/journals/abrep.2020.e220

Abstract

The recombinant antibodies AI334, AQ806 and RB596 detect by immunofluorescence the spike S protein from SARS-CoV-2.

Introduction

The spike (S) glycoprotein mediates attachment of coronaviruses to the host ACE2 receptor (through the Receptor-Binding Domain [RBD] in the S1 subunit) and fusion with the host cell membrane (through the S2 subunit) (Yan et al., 2020). Here we describe the ability of five recombinant antibodies (AR222, AR249, AS274, AS702 and AS708) to detect by ELISA the soluble ectodomain of the S protein from SARS-CoV-2 (UniProt P0DTC2).

Materials & Methods

Antibodies: ABCD_AI334, ABCD_AR222, ABCD_AR249, ABCD_AS273, ABCD_AS274, ABCD_AS702 and ABCD_AS708 antibodies (ABCD nomenclature, http://web.expasy.org/abcd/) were produced by the Geneva Antibody Facility (http://unige.ch/medecine/antibodies/) as mini-antibodies with the antigen-binding portion fused to a mouse IgG2A Fc. The synthesized scFv sequences (GeneArt, Invitrogen) correspond to the sequences of the variable regions joined by a peptide linker (GGGGS)3 (see Table 1 for clone names and references). HEK293 suspension cells (growing in FreeStyle™ 293 Expression Medium, Gibco #12338) were transiently transfected with the vector coding for the scFv-Fc of each antibody. Supernatants (see Table 1 for individual yields) were collected after 4 days.

Antigen: The prefusion ectodomain (residues 1-1208) of the SARS-CoV-2 S protein, with a KV->PP substitution at residues 986/987, a RRAR->GSAS substitution at residues 682-685, and C-terminal T4 fibritin trimerization motif, protease cleavage site, TwinStrepTag and 8xHisTag (PDB #6VSB; Wrapp et al., 2020), was transiently transfected into 25x108 suspension-adapted ExpiCHO cells (Thermo Fisher) using 1.5 mg plasmid DNA and 7.5 mg of PEI MAX (Polysciences) in 500 mL ProCHO5 medium (Lonza). Incubation with agitation was continued at 31°C and 4.5% CO2 for 5 days. The clarified supernatant was purified in two steps: via a Strep-Tactin XT column (IBA Lifesciences) followed by Superose 6 10/300 GL column (GE Healthcare) to a final concentration of 180 µg/ml in PBS.

ABCD Clone Epitope Reference Yield ( mg /L)
AI334 CR3022 S1 ter Meulen et al., 2006 50
AR222 Sb#14 S1/RBD Walter et al., 2020 60
AR249 Sb#45 S1/RBD Walter et al., 2020 100
AS273 B38 S1/RBD Wu et al., 2020 <5
AS274 H4 S1/RBD Wu et al., 2020 20
AS702 CV24 S1 Seydoux et al., 2020 20
AS708 CV30 S1/RBD Seydoux et al., 2020 20
Table 1. Clone number, epitope, reference and production yields for the antibodies used in this study.

Protocol: S protein (10 µg/ml, 50 µl/well in PBS 0.5% (w/v) BSA, 0.1% (w/v) Tween20) was immobilized on streptavidin-coated ELISA plates (Pierce #15124) for 30 min. Each well was rinsed three times with 100 μl of washing buffer (PBS + 0.5% (w/v) BSA + 0.05% (w/v) Tween20), then incubated for 1 hour with 50 µl of each antibody-containing supernatant diluted in washing buffer (Fig. 1). After rinsing 3 times (100 µl washing buffer), wells were incubated with horseradish peroxidase-coupled goat anti-mouse IgG (Bio-Rad #170-6516, dilution 1:1000, 50 μl per well) for 30 min. After 3 rinses, Tetramethylbenzidine (TMB) substrate (Sigma #T5569) was added (50 μl per well). The reaction was stopped by the addition of 25 μl of 2 M H2SO4. The absorbance (OD) was measured at 450 nm, and the absorbance at 570 nm was subtracted.

Results

We tested by ELISA six antibodies recently developed against the SARS-CoV-2 S protein. From these, five (AR222, AR249, AS274, AS702 and AS708) bound in a concentration-dependent manner to the SARS-CoV-2 S protein (Fig. 1). AI334 was used as a positive control (Hammel et al., 2020); AS273 showed no specific binding, most probably due to the fact that this antibody is poorly produced (Table 1, Fig. 1).

Figure 1. Specific binding of AI334, AR222, AR249, AS274, AS702 and AS708 antibodies to the SARS-CoV-2 S protein, as detected by ELISA. On the Y axis, ELISA signal (in arbitrary units). On the X axis, the antibody dilution (1:100, 1:1’000 and 1:10’000). ‘S refers to the binding to the spike S protein; ‘Ctr’ refers to the binding to biotinylated BSA.

Acknowledgments

This work was co-sponsored by NASA TRISH contract #NNX16AO69A/CAT0001. We would like to thank Kelvin Lau, Florence Pojer and Prof. David Hacker (Protein Production and Structure Core Facility, EPFL) for providing the SARS-CoV-2 S protein.

Conflict of interest

The authors declare no conflict of interest.

References

Hammel P, Lau K, Pojer F, Hacker D, Marchetti A. The RB596 antibody recognizes the spike S protein from SARS-CoV-2 by ELISA. Antib. Rep. 2020, 3:e218. doi:10.24450/journals/abrep.2020.e218

ter Meulen J, van den Brink EN, Poon LL, et al. Human monoclonal antibody combination against SARS coronavirus: synergy and coverage of escape mutants. PLoS Med. 2006; 3:e237. PMID:16796401

Wrapp D, De Vlieger D, Corbett KS, et al. Structural basis for potent neutralization of betacoronaviruses by single-domain camelid antibodies. Cell 2020; 181:1004-1015. PMID:32375025

Yan R, Zhang Y, Li Y, Xia L, Guo Y, Zhou Q. Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2. Science 2020; 367:1444-1448. PMID:32132184

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Published

2020-06-23

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Article

How to Cite

1.
Hammel P, Marchetti A, Zenhausern F. AR222, AR249, AS274, AS702 and AS708 antibodies recognize the spike S protein from SARS-CoV-2 by ELISA. Antib. Rep. [Internet]. 2020 Jun. 23 [cited 2024 May 19];3(4):e220. Available from: https://oap.unige.ch/journals/abrep/article/view/220

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