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RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics

A plethora of modified nucleotides extends the chemical and conformational space for natural occurring RNAs. tRNAs constitute the class of RNAs with the highest modification rate. The extensive modification modulates their overall stability, the fidelity and efficiency of translation. However, the i...

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Autores principales: Biedenbänder, Thomas, de Jesus, Vanessa, Schmidt-Dengler, Martina, Helm, Mark, Corzilius, Björn, Fürtig, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8887418/
https://www.ncbi.nlm.nih.gov/pubmed/35137185
http://dx.doi.org/10.1093/nar/gkac040
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author Biedenbänder, Thomas
de Jesus, Vanessa
Schmidt-Dengler, Martina
Helm, Mark
Corzilius, Björn
Fürtig, Boris
author_facet Biedenbänder, Thomas
de Jesus, Vanessa
Schmidt-Dengler, Martina
Helm, Mark
Corzilius, Björn
Fürtig, Boris
author_sort Biedenbänder, Thomas
collection PubMed
description A plethora of modified nucleotides extends the chemical and conformational space for natural occurring RNAs. tRNAs constitute the class of RNAs with the highest modification rate. The extensive modification modulates their overall stability, the fidelity and efficiency of translation. However, the impact of nucleotide modifications on the local structural dynamics is not well characterized. Here we show that the incorporation of the modified nucleotides in tRNA(fMet) from Escherichia coli leads to an increase in the local conformational dynamics, ultimately resulting in the stabilization of the overall tertiary structure. Through analysis of the local dynamics by NMR spectroscopic methods we find that, although the overall thermal stability of the tRNA is higher for the modified molecule, the conformational fluctuations on the local level are increased in comparison to an unmodified tRNA. In consequence, the melting of individual base pairs in the unmodified tRNA is determined by high entropic penalties compared to the modified. Further, we find that the modifications lead to a stabilization of long-range interactions harmonizing the stability of the tRNA’s secondary and tertiary structure. Our results demonstrate that the increase in chemical space through introduction of modifications enables the population of otherwise inaccessible conformational substates.
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spelling pubmed-88874182022-03-02 RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics Biedenbänder, Thomas de Jesus, Vanessa Schmidt-Dengler, Martina Helm, Mark Corzilius, Björn Fürtig, Boris Nucleic Acids Res Structural Biology A plethora of modified nucleotides extends the chemical and conformational space for natural occurring RNAs. tRNAs constitute the class of RNAs with the highest modification rate. The extensive modification modulates their overall stability, the fidelity and efficiency of translation. However, the impact of nucleotide modifications on the local structural dynamics is not well characterized. Here we show that the incorporation of the modified nucleotides in tRNA(fMet) from Escherichia coli leads to an increase in the local conformational dynamics, ultimately resulting in the stabilization of the overall tertiary structure. Through analysis of the local dynamics by NMR spectroscopic methods we find that, although the overall thermal stability of the tRNA is higher for the modified molecule, the conformational fluctuations on the local level are increased in comparison to an unmodified tRNA. In consequence, the melting of individual base pairs in the unmodified tRNA is determined by high entropic penalties compared to the modified. Further, we find that the modifications lead to a stabilization of long-range interactions harmonizing the stability of the tRNA’s secondary and tertiary structure. Our results demonstrate that the increase in chemical space through introduction of modifications enables the population of otherwise inaccessible conformational substates. Oxford University Press 2022-02-07 /pmc/articles/PMC8887418/ /pubmed/35137185 http://dx.doi.org/10.1093/nar/gkac040 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Structural Biology
Biedenbänder, Thomas
de Jesus, Vanessa
Schmidt-Dengler, Martina
Helm, Mark
Corzilius, Björn
Fürtig, Boris
RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics
title RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics
title_full RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics
title_fullStr RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics
title_full_unstemmed RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics
title_short RNA modifications stabilize the tertiary structure of tRNA(fMet) by locally increasing conformational dynamics
title_sort rna modifications stabilize the tertiary structure of trna(fmet) by locally increasing conformational dynamics
topic Structural Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8887418/
https://www.ncbi.nlm.nih.gov/pubmed/35137185
http://dx.doi.org/10.1093/nar/gkac040
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