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Target response controlled enzyme activity switch for multimodal biosensing detection
How to achieve delicate regulation of enzyme activity and empower it with more roles is the peak in the field of enzyme catalysis research. Traditional proteases or novel nano-enzymes are unable to achieve stimulus-responsive activity modulation due to their own structural limitations. Here, we prop...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082497/ https://www.ncbi.nlm.nih.gov/pubmed/37031177 http://dx.doi.org/10.1186/s12951-023-01860-z |
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author | Zhang, Lu Wu, Haiping Chen, Yirong Zhang, Songzhi Song, Mingxuan Liu, Changjin Li, Jia Cheng, Wei Ding, Shijia |
author_facet | Zhang, Lu Wu, Haiping Chen, Yirong Zhang, Songzhi Song, Mingxuan Liu, Changjin Li, Jia Cheng, Wei Ding, Shijia |
author_sort | Zhang, Lu |
collection | PubMed |
description | How to achieve delicate regulation of enzyme activity and empower it with more roles is the peak in the field of enzyme catalysis research. Traditional proteases or novel nano-enzymes are unable to achieve stimulus-responsive activity modulation due to their own structural limitations. Here, we propose a novel Controllable Enzyme Activity Switch, CEAS, based on hemin aggregation regulation, to deeply explore its regulatory mechanism and develop multimodal biosensing applications. The core of CEAS relies on the dimerizable inactivation of catalytically active center hemin and utilizes a DNA template to orderly guide the G4-Hemin DNAzyme to tightly bind to DNA-Hemin, thereby shutting down the catalytic ability. By customizing the design of the guide template, different target stimulus responses lead to hemin dimerization dissociation and restore the synergistic catalysis of G4-Hemin and DNA-Hemin, thus achieving a target-regulated enzymatic activity switch. Moreover, the programmability of CEAS allowed it easy to couple with a variety of DNA recognition and amplification techniques, thus developing a series of visual protein detection systems and highly sensitive fluorescent detection systems with excellent bioanalytical performance. Therefore, the construction of CEAS is expected to break the limitation of conventional enzymes that cannot be targetable regulated, thus enabling customizable enzymatic reaction systems and providing a new paradigm for controllable enzyme activities. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01860-z. |
format | Online Article Text |
id | pubmed-10082497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100824972023-04-09 Target response controlled enzyme activity switch for multimodal biosensing detection Zhang, Lu Wu, Haiping Chen, Yirong Zhang, Songzhi Song, Mingxuan Liu, Changjin Li, Jia Cheng, Wei Ding, Shijia J Nanobiotechnology Research How to achieve delicate regulation of enzyme activity and empower it with more roles is the peak in the field of enzyme catalysis research. Traditional proteases or novel nano-enzymes are unable to achieve stimulus-responsive activity modulation due to their own structural limitations. Here, we propose a novel Controllable Enzyme Activity Switch, CEAS, based on hemin aggregation regulation, to deeply explore its regulatory mechanism and develop multimodal biosensing applications. The core of CEAS relies on the dimerizable inactivation of catalytically active center hemin and utilizes a DNA template to orderly guide the G4-Hemin DNAzyme to tightly bind to DNA-Hemin, thereby shutting down the catalytic ability. By customizing the design of the guide template, different target stimulus responses lead to hemin dimerization dissociation and restore the synergistic catalysis of G4-Hemin and DNA-Hemin, thus achieving a target-regulated enzymatic activity switch. Moreover, the programmability of CEAS allowed it easy to couple with a variety of DNA recognition and amplification techniques, thus developing a series of visual protein detection systems and highly sensitive fluorescent detection systems with excellent bioanalytical performance. Therefore, the construction of CEAS is expected to break the limitation of conventional enzymes that cannot be targetable regulated, thus enabling customizable enzymatic reaction systems and providing a new paradigm for controllable enzyme activities. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-023-01860-z. BioMed Central 2023-04-08 /pmc/articles/PMC10082497/ /pubmed/37031177 http://dx.doi.org/10.1186/s12951-023-01860-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhang, Lu Wu, Haiping Chen, Yirong Zhang, Songzhi Song, Mingxuan Liu, Changjin Li, Jia Cheng, Wei Ding, Shijia Target response controlled enzyme activity switch for multimodal biosensing detection |
title | Target response controlled enzyme activity switch for multimodal biosensing detection |
title_full | Target response controlled enzyme activity switch for multimodal biosensing detection |
title_fullStr | Target response controlled enzyme activity switch for multimodal biosensing detection |
title_full_unstemmed | Target response controlled enzyme activity switch for multimodal biosensing detection |
title_short | Target response controlled enzyme activity switch for multimodal biosensing detection |
title_sort | target response controlled enzyme activity switch for multimodal biosensing detection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082497/ https://www.ncbi.nlm.nih.gov/pubmed/37031177 http://dx.doi.org/10.1186/s12951-023-01860-z |
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