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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,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2021
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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. |
format | Online Article Text |
id | pubmed-7948966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
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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