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Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics
DNAzyme is a class of DNA molecules that can perform catalytic functions with high selectivity towards specific metal ions. Due to its potential applications for biosensors and medical therapeutics, DNAzyme has been extensively studied to characterize the relationships between its biochemical proper...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864658/ https://www.ncbi.nlm.nih.gov/pubmed/36674728 http://dx.doi.org/10.3390/ijms24021212 |
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author | Zhang, Yiming Ji, Zongzhou Wang, Xin Cao, Yi Pan, Hai |
author_facet | Zhang, Yiming Ji, Zongzhou Wang, Xin Cao, Yi Pan, Hai |
author_sort | Zhang, Yiming |
collection | PubMed |
description | DNAzyme is a class of DNA molecules that can perform catalytic functions with high selectivity towards specific metal ions. Due to its potential applications for biosensors and medical therapeutics, DNAzyme has been extensively studied to characterize the relationships between its biochemical properties and functions. Similar to protein enzymes and ribozymes, DNAzymes have been found to undergo conformational changes in a metal–ion–dependent manner for catalysis. Despite the important role the conformation plays in the catalysis process, such structural and dynamic information might not be revealed by conventional approaches. Here, by using the single–molecule fluorescence resonance energy transfer (smFRET) technique, we were able to investigate the detailed conformational dynamics of a uranyl–specific DNAzyme 39E. We observed conformation switches of 39E to a folded state with the addition of Mg(2+) and to an extended state with the addition of UO(2)(2+). Furthermore, 39E can switch to a more compact configuration with or without divalent metal ions. Our findings reveal that 39E can undergo conformational changes spontaneously between different configurations. |
format | Online Article Text |
id | pubmed-9864658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98646582023-01-22 Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics Zhang, Yiming Ji, Zongzhou Wang, Xin Cao, Yi Pan, Hai Int J Mol Sci Article DNAzyme is a class of DNA molecules that can perform catalytic functions with high selectivity towards specific metal ions. Due to its potential applications for biosensors and medical therapeutics, DNAzyme has been extensively studied to characterize the relationships between its biochemical properties and functions. Similar to protein enzymes and ribozymes, DNAzymes have been found to undergo conformational changes in a metal–ion–dependent manner for catalysis. Despite the important role the conformation plays in the catalysis process, such structural and dynamic information might not be revealed by conventional approaches. Here, by using the single–molecule fluorescence resonance energy transfer (smFRET) technique, we were able to investigate the detailed conformational dynamics of a uranyl–specific DNAzyme 39E. We observed conformation switches of 39E to a folded state with the addition of Mg(2+) and to an extended state with the addition of UO(2)(2+). Furthermore, 39E can switch to a more compact configuration with or without divalent metal ions. Our findings reveal that 39E can undergo conformational changes spontaneously between different configurations. MDPI 2023-01-07 /pmc/articles/PMC9864658/ /pubmed/36674728 http://dx.doi.org/10.3390/ijms24021212 Text en © 2023 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 | Article Zhang, Yiming Ji, Zongzhou Wang, Xin Cao, Yi Pan, Hai Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics |
title | Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics |
title_full | Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics |
title_fullStr | Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics |
title_full_unstemmed | Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics |
title_short | Single–Molecule Study of DNAzyme Reveals Its Intrinsic Conformational Dynamics |
title_sort | single–molecule study of dnazyme reveals its intrinsic conformational dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864658/ https://www.ncbi.nlm.nih.gov/pubmed/36674728 http://dx.doi.org/10.3390/ijms24021212 |
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