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Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology
Barnase is an extracellular ribonuclease secreted by Bacillus amyloliquefaciens that was originally studied as a small stable enzyme with robust folding. The identification of barnase intracellular inhibitor barstar led to the discovery of an incredibly strong protein-protein interaction. Together,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625414/ https://www.ncbi.nlm.nih.gov/pubmed/34833876 http://dx.doi.org/10.3390/molecules26226785 |
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author | Shilova, Olga Kotelnikova, Polina Proshkina, Galina Shramova, Elena Deyev, Sergey |
author_facet | Shilova, Olga Kotelnikova, Polina Proshkina, Galina Shramova, Elena Deyev, Sergey |
author_sort | Shilova, Olga |
collection | PubMed |
description | Barnase is an extracellular ribonuclease secreted by Bacillus amyloliquefaciens that was originally studied as a small stable enzyme with robust folding. The identification of barnase intracellular inhibitor barstar led to the discovery of an incredibly strong protein-protein interaction. Together, barnase and barstar provide a fully genetically encoded toxin-antitoxin pair having an extremely low dissociation constant. Moreover, compared to other dimerization systems, the barnase-barstar module provides the exact one-to-one ratio of the complex components and possesses high stability of each component in a complex and high solubility in aqueous solutions without self-aggregation. The unique properties of barnase and barstar allow the application of this pair for the engineering of different variants of targeted anticancer compounds and cytotoxic supramolecular complexes. Using barnase in suicide gene therapy has also found its niche in anticancer therapy. The application of barnase and barstar in contemporary experimental cancer therapy is reflected in the review. |
format | Online Article Text |
id | pubmed-8625414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86254142021-11-27 Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology Shilova, Olga Kotelnikova, Polina Proshkina, Galina Shramova, Elena Deyev, Sergey Molecules Review Barnase is an extracellular ribonuclease secreted by Bacillus amyloliquefaciens that was originally studied as a small stable enzyme with robust folding. The identification of barnase intracellular inhibitor barstar led to the discovery of an incredibly strong protein-protein interaction. Together, barnase and barstar provide a fully genetically encoded toxin-antitoxin pair having an extremely low dissociation constant. Moreover, compared to other dimerization systems, the barnase-barstar module provides the exact one-to-one ratio of the complex components and possesses high stability of each component in a complex and high solubility in aqueous solutions without self-aggregation. The unique properties of barnase and barstar allow the application of this pair for the engineering of different variants of targeted anticancer compounds and cytotoxic supramolecular complexes. Using barnase in suicide gene therapy has also found its niche in anticancer therapy. The application of barnase and barstar in contemporary experimental cancer therapy is reflected in the review. MDPI 2021-11-10 /pmc/articles/PMC8625414/ /pubmed/34833876 http://dx.doi.org/10.3390/molecules26226785 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Shilova, Olga Kotelnikova, Polina Proshkina, Galina Shramova, Elena Deyev, Sergey Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology |
title | Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology |
title_full | Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology |
title_fullStr | Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology |
title_full_unstemmed | Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology |
title_short | Barnase-Barstar Pair: Contemporary Application in Cancer Research and Nanotechnology |
title_sort | barnase-barstar pair: contemporary application in cancer research and nanotechnology |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8625414/ https://www.ncbi.nlm.nih.gov/pubmed/34833876 http://dx.doi.org/10.3390/molecules26226785 |
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