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Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells
Based on previous studies, two antibody-like molecules, monobodies, capable of high-affinity interaction with the SARS-CoV-2 nucleocapsid protein (dissociation constant of tens of nM) were selected. For delivery to target cells, genetically engineered constructs containing monobody and TAT peptide,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Pleiades Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612593/ https://www.ncbi.nlm.nih.gov/pubmed/36303056 http://dx.doi.org/10.1134/S1607672922050088 |
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author | Khramtsov, Y. V. Ulasov, A. V. Lupanova, T. N. Georgiev, G. P. Sobolev, A. S. |
author_facet | Khramtsov, Y. V. Ulasov, A. V. Lupanova, T. N. Georgiev, G. P. Sobolev, A. S. |
author_sort | Khramtsov, Y. V. |
collection | PubMed |
description | Based on previous studies, two antibody-like molecules, monobodies, capable of high-affinity interaction with the SARS-CoV-2 nucleocapsid protein (dissociation constant of tens of nM) were selected. For delivery to target cells, genetically engineered constructs containing monobody and TAT peptide, placed either at the N- or C-terminus of the resulting polypeptide, were produced and expressed in E. coli. The construct with the highest affinity to the SARS-CoV-2 nucleocapsid protein was revealed with the use of thermophoresis technique. Cellular thermal shift assay demonstrated the ability of this construct to interact with the nucleocapsid protein within HEK293T cells transfected with the SARS-CoV-2 nucleocapsid protein fused to the mRuby3 fluorescent protein. Replacement of TAT peptide to S10 shuttle peptide, containing endosomolytic peptide, significantly improved the penetration of the construct into the target cells. |
format | Online Article Text |
id | pubmed-9612593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Pleiades Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-96125932022-10-28 Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells Khramtsov, Y. V. Ulasov, A. V. Lupanova, T. N. Georgiev, G. P. Sobolev, A. S. Dokl Biochem Biophys Biochemistry, Biophysics, and Molecular Biology Based on previous studies, two antibody-like molecules, monobodies, capable of high-affinity interaction with the SARS-CoV-2 nucleocapsid protein (dissociation constant of tens of nM) were selected. For delivery to target cells, genetically engineered constructs containing monobody and TAT peptide, placed either at the N- or C-terminus of the resulting polypeptide, were produced and expressed in E. coli. The construct with the highest affinity to the SARS-CoV-2 nucleocapsid protein was revealed with the use of thermophoresis technique. Cellular thermal shift assay demonstrated the ability of this construct to interact with the nucleocapsid protein within HEK293T cells transfected with the SARS-CoV-2 nucleocapsid protein fused to the mRuby3 fluorescent protein. Replacement of TAT peptide to S10 shuttle peptide, containing endosomolytic peptide, significantly improved the penetration of the construct into the target cells. Pleiades Publishing 2022-10-27 2022 /pmc/articles/PMC9612593/ /pubmed/36303056 http://dx.doi.org/10.1134/S1607672922050088 Text en © Pleiades Publishing, Ltd. 2022, ISSN 1607-6729, Doklady Biochemistry and Biophysics, 2022, Vol. 506, pp. 220–222. © Pleiades Publishing, Ltd., 2022.Russian Text © The Author(s), 2022, published in Doklady Rossiiskoi Akademii Nauk. Nauki o Zhizni, 2022, Vol. 506, pp. 383–386. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Biochemistry, Biophysics, and Molecular Biology Khramtsov, Y. V. Ulasov, A. V. Lupanova, T. N. Georgiev, G. P. Sobolev, A. S. Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells |
title | Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells |
title_full | Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells |
title_fullStr | Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells |
title_full_unstemmed | Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells |
title_short | Delivery of Antibody-Like Molecules, Monobodies, Capable of Binding with SARS-CoV-2 Virus Nucleocapsid Protein, into Target Cells |
title_sort | delivery of antibody-like molecules, monobodies, capable of binding with sars-cov-2 virus nucleocapsid protein, into target cells |
topic | Biochemistry, Biophysics, and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612593/ https://www.ncbi.nlm.nih.gov/pubmed/36303056 http://dx.doi.org/10.1134/S1607672922050088 |
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