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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,...

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Autores principales: Shilova, Olga, Kotelnikova, Polina, Proshkina, Galina, Shramova, Elena, Deyev, Sergey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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