Cargando…
Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution
We perform molecular dynamics simulations, based on recent crystallographic data, on the 8–17 DNAzyme at four states along the reaction pathway to determine the dynamical ensemble for the active state and transition state mimic in solution. A striking finding is the diverse roles played by Na(+) and...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821293/ https://www.ncbi.nlm.nih.gov/pubmed/31511899 http://dx.doi.org/10.1093/nar/gkz773 |
_version_ | 1783464117921644544 |
---|---|
author | Ekesan, Şölen York, Darrin M |
author_facet | Ekesan, Şölen York, Darrin M |
author_sort | Ekesan, Şölen |
collection | PubMed |
description | We perform molecular dynamics simulations, based on recent crystallographic data, on the 8–17 DNAzyme at four states along the reaction pathway to determine the dynamical ensemble for the active state and transition state mimic in solution. A striking finding is the diverse roles played by Na(+) and Pb(2+) ions in the electrostatically strained active site that impact all four fundamental catalytic strategies, and share commonality with some features recently inferred for naturally occurring hammerhead and pistol ribozymes. The active site Pb(2+) ion helps to stabilize in-line nucleophilic attack, provides direct electrostatic transition state stabilization, and facilitates leaving group departure. A conserved guanine residue is positioned to act as the general base, and is assisted by a bridging Na(+) ion that tunes the pK(a) and facilitates in-line fitness. The present work provides insight into how DNA molecules are able to solve the RNA-cleavage problem, and establishes functional relationships between the mechanism of these engineered DNA enzymes with their naturally evolved RNA counterparts. This adds valuable information to our growing body of knowledge on general mechanisms of phosphoryl transfer reactions catalyzed by RNA, proteins and DNA. |
format | Online Article Text |
id | pubmed-6821293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68212932019-11-04 Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution Ekesan, Şölen York, Darrin M Nucleic Acids Res Nucleic Acid Enzymes We perform molecular dynamics simulations, based on recent crystallographic data, on the 8–17 DNAzyme at four states along the reaction pathway to determine the dynamical ensemble for the active state and transition state mimic in solution. A striking finding is the diverse roles played by Na(+) and Pb(2+) ions in the electrostatically strained active site that impact all four fundamental catalytic strategies, and share commonality with some features recently inferred for naturally occurring hammerhead and pistol ribozymes. The active site Pb(2+) ion helps to stabilize in-line nucleophilic attack, provides direct electrostatic transition state stabilization, and facilitates leaving group departure. A conserved guanine residue is positioned to act as the general base, and is assisted by a bridging Na(+) ion that tunes the pK(a) and facilitates in-line fitness. The present work provides insight into how DNA molecules are able to solve the RNA-cleavage problem, and establishes functional relationships between the mechanism of these engineered DNA enzymes with their naturally evolved RNA counterparts. This adds valuable information to our growing body of knowledge on general mechanisms of phosphoryl transfer reactions catalyzed by RNA, proteins and DNA. Oxford University Press 2019-11-04 2019-09-12 /pmc/articles/PMC6821293/ /pubmed/31511899 http://dx.doi.org/10.1093/nar/gkz773 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Nucleic Acid Enzymes Ekesan, Şölen York, Darrin M Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution |
title | Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution |
title_full | Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution |
title_fullStr | Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution |
title_full_unstemmed | Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution |
title_short | Dynamical ensemble of the active state and transition state mimic for the RNA-cleaving 8–17 DNAzyme in solution |
title_sort | dynamical ensemble of the active state and transition state mimic for the rna-cleaving 8–17 dnazyme in solution |
topic | Nucleic Acid Enzymes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821293/ https://www.ncbi.nlm.nih.gov/pubmed/31511899 http://dx.doi.org/10.1093/nar/gkz773 |
work_keys_str_mv | AT ekesansolen dynamicalensembleoftheactivestateandtransitionstatemimicforthernacleaving817dnazymeinsolution AT yorkdarrinm dynamicalensembleoftheactivestateandtransitionstatemimicforthernacleaving817dnazymeinsolution |