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Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone

DEAD-box proteins are nonprocessive RNA helicases that can function as RNA chaperones by coupling ATP binding and hydrolysis to structural reorganization of RNA. Here, Jarmoskaite et al. quantify the ATP utilization of an RNA chaperone during refolding of a misfolded ribozyme substrate. Strikingly,...

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Detalles Bibliográficos
Autores principales: Duran, Elizabeth C., Walter, Nils G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948966/
https://www.ncbi.nlm.nih.gov/pubmed/33837746
http://dx.doi.org/10.1016/j.jbc.2021.100265
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author Duran, Elizabeth C.
Walter, Nils G.
author_facet Duran, Elizabeth C.
Walter, Nils G.
author_sort Duran, Elizabeth C.
collection PubMed
description DEAD-box proteins are nonprocessive RNA helicases that can function as RNA chaperones by coupling ATP binding and hydrolysis to structural reorganization of RNA. Here, Jarmoskaite et al. quantify the ATP utilization of an RNA chaperone during refolding of a misfolded ribozyme substrate. Strikingly, 100 ATP hydrolysis events are needed per successfully refolded ribozyme, suggesting that each round of unfolding requires ten ATP molecules, since 90% of substrate unfolding cycles only lead back to the kinetically favored misfolded state. This near-Sisyphean effort reveals a potentially conserved model for RNA reorganization by RNA chaperones.
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spelling pubmed-79489662021-03-19 Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone Duran, Elizabeth C. Walter, Nils G. J Biol Chem Editors' Pick Highlight DEAD-box proteins are nonprocessive RNA helicases that can function as RNA chaperones by coupling ATP binding and hydrolysis to structural reorganization of RNA. Here, Jarmoskaite et al. quantify the ATP utilization of an RNA chaperone during refolding of a misfolded ribozyme substrate. Strikingly, 100 ATP hydrolysis events are needed per successfully refolded ribozyme, suggesting that each round of unfolding requires ten ATP molecules, since 90% of substrate unfolding cycles only lead back to the kinetically favored misfolded state. This near-Sisyphean effort reveals a potentially conserved model for RNA reorganization by RNA chaperones. American Society for Biochemistry and Molecular Biology 2021-02-11 /pmc/articles/PMC7948966/ /pubmed/33837746 http://dx.doi.org/10.1016/j.jbc.2021.100265 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Editors' Pick Highlight
Duran, Elizabeth C.
Walter, Nils G.
Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone
title Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone
title_full Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone
title_fullStr Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone
title_full_unstemmed Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone
title_short Sisyphus observed: Unraveling the high ATP usage of an RNA chaperone
title_sort sisyphus observed: unraveling the high atp usage of an rna chaperone
topic Editors' Pick Highlight
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948966/
https://www.ncbi.nlm.nih.gov/pubmed/33837746
http://dx.doi.org/10.1016/j.jbc.2021.100265
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