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Stem–loop formation drives RNA folding in mechanical unzipping experiments
Accurate knowledge of RNA hybridization is essential for understanding RNA structure and function. Here we mechanically unzip and rezip a 2-kbp RNA hairpin and derive the 10 nearest-neighbor base pair (NNBP) RNA free energies in sodium and magnesium with 0.1 kcal/mol precision using optical tweezers...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784153/ https://www.ncbi.nlm.nih.gov/pubmed/35022230 http://dx.doi.org/10.1073/pnas.2025575119 |
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author | Rissone, Paolo Bizarro, Cristiano V. Ritort, Felix |
author_facet | Rissone, Paolo Bizarro, Cristiano V. Ritort, Felix |
author_sort | Rissone, Paolo |
collection | PubMed |
description | Accurate knowledge of RNA hybridization is essential for understanding RNA structure and function. Here we mechanically unzip and rezip a 2-kbp RNA hairpin and derive the 10 nearest-neighbor base pair (NNBP) RNA free energies in sodium and magnesium with 0.1 kcal/mol precision using optical tweezers. Notably, force–distance curves (FDCs) exhibit strong irreversible effects with hysteresis and several intermediates, precluding the extraction of the NNBP energies with currently available methods. The combination of a suitable RNA synthesis with a tailored pulling protocol allowed us to obtain the fully reversible FDCs necessary to derive the NNBP energies. We demonstrate the equivalence of sodium and magnesium free-energy salt corrections at the level of individual NNBP. To characterize the irreversibility of the unzipping–rezipping process, we introduce a barrier energy landscape of the stem–loop structures forming along the complementary strands, which compete against the formation of the native hairpin. This landscape correlates with the hysteresis observed along the FDCs. RNA sequence analysis shows that base stacking and base pairing stabilize the stem–loops that kinetically trap the long-lived intermediates observed in the FDC. Stem–loops formation appears as a general mechanism to explain a wide range of behaviors observed in RNA folding. |
format | Online Article Text |
id | pubmed-8784153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-87841532022-07-11 Stem–loop formation drives RNA folding in mechanical unzipping experiments Rissone, Paolo Bizarro, Cristiano V. Ritort, Felix Proc Natl Acad Sci U S A Biological Sciences Accurate knowledge of RNA hybridization is essential for understanding RNA structure and function. Here we mechanically unzip and rezip a 2-kbp RNA hairpin and derive the 10 nearest-neighbor base pair (NNBP) RNA free energies in sodium and magnesium with 0.1 kcal/mol precision using optical tweezers. Notably, force–distance curves (FDCs) exhibit strong irreversible effects with hysteresis and several intermediates, precluding the extraction of the NNBP energies with currently available methods. The combination of a suitable RNA synthesis with a tailored pulling protocol allowed us to obtain the fully reversible FDCs necessary to derive the NNBP energies. We demonstrate the equivalence of sodium and magnesium free-energy salt corrections at the level of individual NNBP. To characterize the irreversibility of the unzipping–rezipping process, we introduce a barrier energy landscape of the stem–loop structures forming along the complementary strands, which compete against the formation of the native hairpin. This landscape correlates with the hysteresis observed along the FDCs. RNA sequence analysis shows that base stacking and base pairing stabilize the stem–loops that kinetically trap the long-lived intermediates observed in the FDC. Stem–loops formation appears as a general mechanism to explain a wide range of behaviors observed in RNA folding. National Academy of Sciences 2022-01-11 2022-01-18 /pmc/articles/PMC8784153/ /pubmed/35022230 http://dx.doi.org/10.1073/pnas.2025575119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Rissone, Paolo Bizarro, Cristiano V. Ritort, Felix Stem–loop formation drives RNA folding in mechanical unzipping experiments |
title | Stem–loop formation drives RNA folding in mechanical unzipping experiments |
title_full | Stem–loop formation drives RNA folding in mechanical unzipping experiments |
title_fullStr | Stem–loop formation drives RNA folding in mechanical unzipping experiments |
title_full_unstemmed | Stem–loop formation drives RNA folding in mechanical unzipping experiments |
title_short | Stem–loop formation drives RNA folding in mechanical unzipping experiments |
title_sort | stem–loop formation drives rna folding in mechanical unzipping experiments |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8784153/ https://www.ncbi.nlm.nih.gov/pubmed/35022230 http://dx.doi.org/10.1073/pnas.2025575119 |
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