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. 2022 Apr;503(1):90-92.
doi: 10.1134/S1607672922020077. Epub 2022 May 10.

Among Antibody-Like Molecules, Monobodies, Able to Interact with Nucleocapsid Protein of SARS-CoV Virus, There Are Monobodies with High Affinity to Nucleocapsid Protein of SARS-CoV-2 Virus

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Among Antibody-Like Molecules, Monobodies, Able to Interact with Nucleocapsid Protein of SARS-CoV Virus, There Are Monobodies with High Affinity to Nucleocapsid Protein of SARS-CoV-2 Virus

Y V Khramtsov et al. Dokl Biochem Biophys. 2022 Apr.

Abstract

Seven amino acid sequences of antibody mimetics molecules, monobodies, capable of interacting with the nucleocapsid protein of the SARS-CoV virus, were taken from the literature. Nucleotide sequences of monobody genes were obtained by gene synthesis, which were expressed in E. coli and isolated using Ni-NTA chromatography. It was shown by thermophoresis that three of the seven selected antibody-like molecules can interact with high affinity (dissociation constant of tens of nM) with the nucleocapsid protein of the SARS-CoV-2 virus. For the remaining four monobodies, only low affinity binding with a dissociation constant of several μM was found.

Keywords: SARS-CoV; SARS-CoV-2; antibody-like molecules; monobody; nucleocapsid protein; thermophoresis.

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Conflict of interest statement

The authors declare that they have no conflicts of interest. This article does not contain any studies involving animals or human participants performed by any of the authors.

Figures

Fig. 1.
Fig. 1.
Dependences of relative fluorescence (fluorescence before the start of thermophoresis was taken as 100%) 20 s after the start of thermophoresis on the concentration of Fn-N at a constant concentration of N protein (40 nM) for Fn-N with low affinity for the N protein (a) and with high affinity for the N protein (b). SEs of relative fluorescence are shown (8–12 replicates).

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References

    1. Clercq E.D., Li G. Clin. Microbiol. Rev. 2016;29:695–747. doi: 10.1128/CMR.00102-15. - DOI - PMC - PubMed
    1. Gebauer M., Skerra A. Annu. Rev. Pharmacol. Toxicol. 2020;60:391–415. doi: 10.1146/annurev-pharmtox-010818-021118. - DOI - PubMed
    1. Surjit M., Lal S.K. Infect. Genet. Evol. 2008;8:397–405. doi: 10.1016/j.meegid.2007.07.004. - DOI - PMC - PubMed
    1. Wu, C. and Zheng, M., Preprints, 2020, no. 2020020247.
    1. Prajapat M., Sarma P., Shekhar N. Indian J. Pharmacol. 2020;52:56. doi: 10.4103/ijp.IJP_115_20. - DOI - PMC - PubMed