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Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq

Under the oxidative stress condition, the small RNA (sRNA) OxyS that acts as essential post-transcriptional regulators of gene expression is produced and plays a regulatory function with the assistance of the RNA chaperone Hfq protein. Interestingly, experimental studies found that the N48A mutation...

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Autores principales: Li, Mengxin, Cong, Yalong, Qi, Yifei, Zhang, John Z. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615722/
https://www.ncbi.nlm.nih.gov/pubmed/34827651
http://dx.doi.org/10.3390/biom11111653
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author Li, Mengxin
Cong, Yalong
Qi, Yifei
Zhang, John Z. H.
author_facet Li, Mengxin
Cong, Yalong
Qi, Yifei
Zhang, John Z. H.
author_sort Li, Mengxin
collection PubMed
description Under the oxidative stress condition, the small RNA (sRNA) OxyS that acts as essential post-transcriptional regulators of gene expression is produced and plays a regulatory function with the assistance of the RNA chaperone Hfq protein. Interestingly, experimental studies found that the N48A mutation of Hfq protein could enhance the binding affinity with OxyS while resulting in the defection of gene regulation. However, how the Hfq protein interacts with sRNA OxyS and the origin of the stronger affinity of N48A mutation are both unclear. In this paper, molecular dynamics (MD) simulations were performed on the complex structure of Hfq and OxyS to explore their binding mechanism. The molecular mechanics generalized born surface area (MM/GBSA) and interaction entropy (IE) method were combined to calculate the binding free energy between Hfq and OxyS sRNA, and the computational result was correlated with the experimental result. Per-residue decomposition of the binding free energy revealed that the enhanced binding ability of the N48A mutation mainly came from the increased van der Waals interactions (vdW). This research explored the binding mechanism between Oxys and chaperone protein Hfq and revealed the origin of the strong binding affinity of N48A mutation. The results provided important insights into the mechanism of gene expression regulation affected by protein mutations.
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spelling pubmed-86157222021-11-26 Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq Li, Mengxin Cong, Yalong Qi, Yifei Zhang, John Z. H. Biomolecules Article Under the oxidative stress condition, the small RNA (sRNA) OxyS that acts as essential post-transcriptional regulators of gene expression is produced and plays a regulatory function with the assistance of the RNA chaperone Hfq protein. Interestingly, experimental studies found that the N48A mutation of Hfq protein could enhance the binding affinity with OxyS while resulting in the defection of gene regulation. However, how the Hfq protein interacts with sRNA OxyS and the origin of the stronger affinity of N48A mutation are both unclear. In this paper, molecular dynamics (MD) simulations were performed on the complex structure of Hfq and OxyS to explore their binding mechanism. The molecular mechanics generalized born surface area (MM/GBSA) and interaction entropy (IE) method were combined to calculate the binding free energy between Hfq and OxyS sRNA, and the computational result was correlated with the experimental result. Per-residue decomposition of the binding free energy revealed that the enhanced binding ability of the N48A mutation mainly came from the increased van der Waals interactions (vdW). This research explored the binding mechanism between Oxys and chaperone protein Hfq and revealed the origin of the strong binding affinity of N48A mutation. The results provided important insights into the mechanism of gene expression regulation affected by protein mutations. MDPI 2021-11-08 /pmc/articles/PMC8615722/ /pubmed/34827651 http://dx.doi.org/10.3390/biom11111653 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Li, Mengxin
Cong, Yalong
Qi, Yifei
Zhang, John Z. H.
Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq
title Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq
title_full Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq
title_fullStr Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq
title_full_unstemmed Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq
title_short Computational Insights into the Binding Mechanism of OxyS sRNA with Chaperone Protein Hfq
title_sort computational insights into the binding mechanism of oxys srna with chaperone protein hfq
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8615722/
https://www.ncbi.nlm.nih.gov/pubmed/34827651
http://dx.doi.org/10.3390/biom11111653
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