Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Rissone, Paolo, Bizarro, Cristiano V., Ritort, Felix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
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
_version_ 1784638672098820096
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
work_keys_str_mv AT rissonepaolo stemloopformationdrivesrnafoldinginmechanicalunzippingexperiments
AT bizarrocristianov stemloopformationdrivesrnafoldinginmechanicalunzippingexperiments
AT ritortfelix stemloopformationdrivesrnafoldinginmechanicalunzippingexperiments