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Structure and mechanism of a methyltransferase ribozyme
Known ribozymes in contemporary biology perform a limited range of chemical catalysis, but in vitro selection has generated species that catalyze a broader range of chemistry; yet, there have been few structural and mechanistic studies of selected ribozymes. A ribozyme has recently been selected tha...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050513/ https://www.ncbi.nlm.nih.gov/pubmed/35301479 http://dx.doi.org/10.1038/s41589-022-00982-z |
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author | Deng, Jie Wilson, Timothy J. Wang, Jia Peng, Xuemei Li, Mengxiao Lin, Xiaowei Liao, Wenjian Lilley, David M. J. Huang, Lin |
author_facet | Deng, Jie Wilson, Timothy J. Wang, Jia Peng, Xuemei Li, Mengxiao Lin, Xiaowei Liao, Wenjian Lilley, David M. J. Huang, Lin |
author_sort | Deng, Jie |
collection | PubMed |
description | Known ribozymes in contemporary biology perform a limited range of chemical catalysis, but in vitro selection has generated species that catalyze a broader range of chemistry; yet, there have been few structural and mechanistic studies of selected ribozymes. A ribozyme has recently been selected that can catalyze a site-specific methyl transfer reaction. We have solved the crystal structure of this ribozyme at a resolution of 2.3 Å, showing how the RNA folds to generate a very specific binding site for the methyl donor substrate. The structure immediately suggests a catalytic mechanism involving a combination of proximity and orientation and nucleobase-mediated general acid catalysis. The mechanism is supported by the pH dependence of the rate of catalysis. A selected methyltransferase ribozyme can thus use a relatively sophisticated catalytic mechanism, broadening the range of known RNA-catalyzed chemistry. [Image: see text] |
format | Online Article Text |
id | pubmed-9050513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-90505132022-04-30 Structure and mechanism of a methyltransferase ribozyme Deng, Jie Wilson, Timothy J. Wang, Jia Peng, Xuemei Li, Mengxiao Lin, Xiaowei Liao, Wenjian Lilley, David M. J. Huang, Lin Nat Chem Biol Article Known ribozymes in contemporary biology perform a limited range of chemical catalysis, but in vitro selection has generated species that catalyze a broader range of chemistry; yet, there have been few structural and mechanistic studies of selected ribozymes. A ribozyme has recently been selected that can catalyze a site-specific methyl transfer reaction. We have solved the crystal structure of this ribozyme at a resolution of 2.3 Å, showing how the RNA folds to generate a very specific binding site for the methyl donor substrate. The structure immediately suggests a catalytic mechanism involving a combination of proximity and orientation and nucleobase-mediated general acid catalysis. The mechanism is supported by the pH dependence of the rate of catalysis. A selected methyltransferase ribozyme can thus use a relatively sophisticated catalytic mechanism, broadening the range of known RNA-catalyzed chemistry. [Image: see text] Nature Publishing Group US 2022-03-17 2022 /pmc/articles/PMC9050513/ /pubmed/35301479 http://dx.doi.org/10.1038/s41589-022-00982-z Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Deng, Jie Wilson, Timothy J. Wang, Jia Peng, Xuemei Li, Mengxiao Lin, Xiaowei Liao, Wenjian Lilley, David M. J. Huang, Lin Structure and mechanism of a methyltransferase ribozyme |
title | Structure and mechanism of a methyltransferase ribozyme |
title_full | Structure and mechanism of a methyltransferase ribozyme |
title_fullStr | Structure and mechanism of a methyltransferase ribozyme |
title_full_unstemmed | Structure and mechanism of a methyltransferase ribozyme |
title_short | Structure and mechanism of a methyltransferase ribozyme |
title_sort | structure and mechanism of a methyltransferase ribozyme |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050513/ https://www.ncbi.nlm.nih.gov/pubmed/35301479 http://dx.doi.org/10.1038/s41589-022-00982-z |
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