Molecular Immunology2022,Vol.14110.DOI:10.1016/j.molimm.2021.12.006

Generation and utility of a single-chain fragment variable monoclonal antibody platform against a baculovirus expressed recombinant receptor binding domain of SARS-CoV-2 spike protein

Salem R. El-Kholy A.A. Waly F.R. Ayman D. Sakr A. Hussein M.
Molecular Immunology2022,Vol.14110.DOI:10.1016/j.molimm.2021.12.006

Generation and utility of a single-chain fragment variable monoclonal antibody platform against a baculovirus expressed recombinant receptor binding domain of SARS-CoV-2 spike protein

Salem R. 1El-Kholy A.A. 2Waly F.R. 1Ayman D. 1Sakr A. 1Hussein M.1
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作者信息

  • 1. Agricultural Genetic Engineering Research Institute (AGERI) ARC
  • 2. Veterinary Sera and Vaccines Research Institute (VSVRI) ARC
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Abstract

? 2021 Elsevier LtdAs the second wave of COVID-19 launched, various variants of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have emerged with a dramatic global spread amongst millions of people causing unprecedented case fatalities and economic shut-downs. That initiated a necessity for developing specific diagnostics and therapeutics along with vaccines to control such a pandemic. This endeavor describes generation of murine derived recombinant single-chain fragment variable (scFv) as a monoclonal antibody (MAb) platform targeting the receptor binding domain (RBD) of Spike protein of SARS-CoV-2. A specific synthesized RBD coding sequence was cloned and expressed in Baculovirus expression system. The recombinant RBD (rRBD) was ascertained to be at the proper encoding size of ~ 600bp and expressed protein of the molecular weight of ~ 21KDa. Purified rRBD was proved genuinely antigenic and immunogenic, exhibiting specific reactivity to anti-SARS-CoV-2 antibody in an indirect enzyme-linked immunosorbent assay (ELISA), and inducing strong seroconversion in immunized mice. The scFv phage display library against rRBD was successfully constructed, revealing ~ 90 % recombination frequency, and great enriching factor reaching 88 % and 25 % in polyclonal Ab-based and MAb-based ELISAs, respectively. Typically, three unique scFvs were generated, selected, purified and molecularly identified. That was manifested by their: accurate structure, close relation to the mouse immunoglobulin (Ig) superfamily, right anchored six complementarily-determining regions (CDRs) as three within variable heavy (vH) and variable light (vL) regions each, and proper configuration of the three-dimensional (3D) structure. Besides, their expression downstream in a non-suppressive amber codon of E. coli strain SS32 created a distinct protein band at an apparent molecular weight of ~ 27KDa. Moreover, the purified scFvs showed authentic immunoreactivity and specificity to both rRBD and SARS-CoV-2 in western blot and ELISA. Accordingly, these developed scFvs platform might be a functional candidate for research, inexpensive diagnostics and therapeutics, mitigating spread of COVID-19.

Key words

Baculovirus expression vector system/COVID-19/Murine scFv antibodies/Phage display/Recombinant RBD/SARS-CoV-2

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出版年

2022
Molecular Immunology

Molecular Immunology

ISTP
ISSN:0161-5890
被引量2
参考文献量54
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