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Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein

Bacillus subtilis spores are considered to be efficient and useful vehicles for the surface display and delivery of heterologous proteins. In this study, we prepared recombinant spores with the receptor binding domain (RBD) of the SARS-CoV-2 spike glycoprotein displayed on their surface in fusion wi...

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Detalles Bibliográficos
Autores principales: Vetráková, A., Chovanová, R. Kalianková, Rechtoríková, R., Krajčíková, D., Barák, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9904849/
https://www.ncbi.nlm.nih.gov/pubmed/36778063
http://dx.doi.org/10.1016/j.csbj.2023.02.007
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author Vetráková, A.
Chovanová, R. Kalianková
Rechtoríková, R.
Krajčíková, D.
Barák, I.
author_facet Vetráková, A.
Chovanová, R. Kalianková
Rechtoríková, R.
Krajčíková, D.
Barák, I.
author_sort Vetráková, A.
collection PubMed
description Bacillus subtilis spores are considered to be efficient and useful vehicles for the surface display and delivery of heterologous proteins. In this study, we prepared recombinant spores with the receptor binding domain (RBD) of the SARS-CoV-2 spike glycoprotein displayed on their surface in fusion with the CotZ or CotY spore coat proteins as a possible tool for the development of an oral vaccine against the SARS-CoV-2 virus. The RBD was attached to the N-terminus or C-terminus of the coat proteins. We also directly adsorbed non-recombinantly produced RBD to the spore surface. SDS-PAGE, western blot and fluorescence microscopy were used to analyze RBD surface expression on purified spores. Results obtained from both display systems, recombinant and non-recombinant, demonstrated that RBD was present on the spore surfaces.
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spelling pubmed-99048492023-02-08 Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein Vetráková, A. Chovanová, R. Kalianková Rechtoríková, R. Krajčíková, D. Barák, I. Comput Struct Biotechnol J Research Article Bacillus subtilis spores are considered to be efficient and useful vehicles for the surface display and delivery of heterologous proteins. In this study, we prepared recombinant spores with the receptor binding domain (RBD) of the SARS-CoV-2 spike glycoprotein displayed on their surface in fusion with the CotZ or CotY spore coat proteins as a possible tool for the development of an oral vaccine against the SARS-CoV-2 virus. The RBD was attached to the N-terminus or C-terminus of the coat proteins. We also directly adsorbed non-recombinantly produced RBD to the spore surface. SDS-PAGE, western blot and fluorescence microscopy were used to analyze RBD surface expression on purified spores. Results obtained from both display systems, recombinant and non-recombinant, demonstrated that RBD was present on the spore surfaces. Research Network of Computational and Structural Biotechnology 2023-02-08 /pmc/articles/PMC9904849/ /pubmed/36778063 http://dx.doi.org/10.1016/j.csbj.2023.02.007 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Vetráková, A.
Chovanová, R. Kalianková
Rechtoríková, R.
Krajčíková, D.
Barák, I.
Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein
title Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein
title_full Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein
title_fullStr Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein
title_full_unstemmed Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein
title_short Bacillus subtilis spores displaying RBD domain of SARS-CoV-2 spike protein
title_sort bacillus subtilis spores displaying rbd domain of sars-cov-2 spike protein
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9904849/
https://www.ncbi.nlm.nih.gov/pubmed/36778063
http://dx.doi.org/10.1016/j.csbj.2023.02.007
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