AI334, AQ806, AR222, AR249, AS274, AS708, RB572, RB574 and RB596 antibodies recognize SARS-CoV-2 viral particles by dot blot

Authors

  • Jerome Lacombe
  • Frederic Zenhausern
  • Pierre Cosson

DOI:

https://doi.org/10.24450/journals/abrep.2020.e273

Abstract

The recombinant antibodies AI334, AQ806, AR222, AR249, AS274, AS708, RB572, RB574 and RB596 detect inactivated SARS-CoV-2 viral particles by dot blot.

Introduction

SARS-CoV-2, a new member of the Coronaviridae family, emerged in China in December 2019, and has since caused an unprecedented world pandemic (Coronaviridae Study Group of the International Committee on Taxonomy of Viruses, 2020). Here we describe the ability of nine recombinant antibodies (AI334, AQ806, AR222, AR249, AS274, AS708, RB572, RB574 and RB596) to successfully detect by dot blot inactivated SARS-CoV-2 viral particles.

Materials & Methods

Antibodies: ABCD_AI334, ABCD_AQ806, ABCD_AR222, ABCD_AR249, ABCD_AS274, ABCD_AS708, ABCD_RB572, ABCD_RB574 and ABCD_RB596 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 or VHH 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). HEK 293T suspension cells (growing in FreeStyle™ 293 Expression Medium, Gibco 12338) were transiently transfected with the vector coding for the scFv-Fc or VHH-Fc of each antibody. Supernatants (see Table 1 for individual yields) were collected after 4 days.

ABCD Clone Epitope Reference Yield (mg/L)
AI334 CR3022 S1 ter Meulen et al., 2006 50
AQ806 VHH-72 S1 Wrapp et al., 2020 50
AR222 Sb#14 S1 Walter et al., 2020 60
AR249 Sb#45 S1 Walter et al., 2020 100
AS274 H4 S1 Wu et al., 2020 20
AS708 CV30 S1 Seydoux et al., 2020 20
RB572 MRB572 M Hammel and Zenhausern, 2020 10
RB574 MRB574 M Hammel and Zenhausern, 2020 10
RB596 MRB596 S2 Farrera-Soler et al., 2020 100
Table 1. Clone number, epitope, reference and production yields for the antibodies used in this study.

Antigen: Inactivated SARS-CoV-2 viral particles were obtained from BEI Resources (NIAID/NIH, NR-52287). They consist of a gamma-irradiated and sonicated cell lysate and supernatant from Vero-E6 cells infected with SARS-CoV-2 (isolate USA-WA1/2020).

Protocol:A droplet of viral particles was deposited (2 µl of undiluted and of 1:5 and 1:25 dilutions) on a 0.45 µm nitrocellulose membrane (Amersham Protran Premium 10600003), and air dried for 5 min. The membrane was blocked for 1 h in PBS containing 0.1% (v/v) Tween20 and 3% (w/v) milk, and washed once for 15 minutes in PBS + 0.1% (v/v) Tween20 (PBS-Tween). The membrane was then incubated overnight (16 h) at RT with the indicated antibodies (final concentration 5 mg/L in PBS-Tween). The membrane was washed three times (15+15+10 min) in PBS-Tween, incubated for 1 h with horseradish peroxidase-coupled goat anti-mouse IgG (Biorad, 170-6516, dilution 1:3000) and washed three times (15 min) in PBS-Tween. The signal was revealed by enhanced chemiluminescence (ECL) (Amersham Biosciences) using a PXi-4 gel imaging systems (Syngene). All membranes were handled in parallel and exposed together to allow direct comparison of the signal generated by different antibodies.

Results

Antibodies AI334, AQ806, AR222, AR249, AS274, AS708 and, to a lesser extent, RB572, RB574, and RB596 recognize inactivated SARS-CoV-2 viral particles in Vero-E6 cells by dot blot (Fig. 1). An antibody against an irrelevant target (AL626, against the ALFA epitope; Lamrabet, 2020) did not detect any signal (Fig. 1). Two of the antibodies tested here recognize the cytosolic domain of the M protein (RB572 and RB574); the relatively low signal obtained with these antibodies may be due to the fact that the corresponding epitopes are embedded in the virus structure and less accessible to the antibodies.

Figure 1. Antibodies AI334, AQ806, AR222, AR249, AS274, AS708, RB572, RB574 and RB596 recognize inactivated SARS-CoV-2 viral particles in a concentration-dependent manner (concentration of the viral drop deposited: 1:1, 1:5 and 1:25; 2 µl/spot). The negative control antibody AL626 (against an irrelevant target) does not detect any signal.

Acknowledgments

This work was co-sponsored by NASA TRISH contract #NNX16AO69A/CAT0001. The following reagents were deposited by the Centers for Disease Control and Prevention and obtained through BEI Resources, NIAID, NIH: SARS-Related Coronavirus 2, Isolate USA-WA1/2020, Gamma-Irradiated, NR-52287.

Conflict of interest

Pierre Cosson is an editor of the Antibody Reports journal.

References

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Farrera-Soler L, Daguer JP, Barluenga S, Winssinger N. The RB596 antibody recognizes a linear epitope from the spike S protein from SARS-CoV-2. Antib. Rep. 2020, 3:e232. doi:10.24450/journals/abrep.2020.e232

Hammel P, Zenhausern F. RB571, RB572, RB573, RB574, RB575, RB576, RB577 and RB578 antibodies recognize a fragment of the membrane M protein from SARS-CoV-2 by ELISA. Antib. Rep. 2020, 3:e230. doi:10.24450/journals/abrep.2020.e230

Lamrabet O. The AL626 antibody recognizes an ALFA-tagged protein by western blot. Antib. Rep. 2020, 3:e123. doi:10.24450/journals/abrep.2020.e123

Seydoux E, Homad LJ, MacCamy AJ, et al. Analysis of a SARS-CoV-2-infected individual reveals development of potent neutralizing antibodies with limited somatic mutation. Immunity 2020; 53:1-8. PMID: 32561270.

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

Walter JD, Hutter CAJ, Zimmermann I, et al. Sybodies targeting the SARS-CoV-2 receptor-binding domain. Preprint. bioRxiv 2020; 2020.04.16.045419. doi:10.1101/2020.04.16.045419

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Published

2020-12-15

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Article

How to Cite

1.
Lacombe J, Zenhausern F, Cosson P. AI334, AQ806, AR222, AR249, AS274, AS708, RB572, RB574 and RB596 antibodies recognize SARS-CoV-2 viral particles by dot blot. Antib. Rep. [Internet]. 2020 Dec. 15 [cited 2024 May 27];3(4):e273. Available from: https://oap.unige.ch/journals/abrep/article/view/273

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