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Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor
Reversible switching of the bacterial flagellar motor between clockwise (CW) and counterclockwise (CCW) rotation is necessary for chemotaxis, which enables cells to swim towards favorable chemical habitats. Increase in the viscous resistance to the rotation of the motor (mechanical load) inhibits sw...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440544/ https://www.ncbi.nlm.nih.gov/pubmed/34521846 http://dx.doi.org/10.1038/s41467-021-25774-2 |
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author | Antani, Jyot D. Gupta, Rachit Lee, Annie H. Rhee, Kathy Y. Manson, Michael D. Lele, Pushkar P. |
author_facet | Antani, Jyot D. Gupta, Rachit Lee, Annie H. Rhee, Kathy Y. Manson, Michael D. Lele, Pushkar P. |
author_sort | Antani, Jyot D. |
collection | PubMed |
description | Reversible switching of the bacterial flagellar motor between clockwise (CW) and counterclockwise (CCW) rotation is necessary for chemotaxis, which enables cells to swim towards favorable chemical habitats. Increase in the viscous resistance to the rotation of the motor (mechanical load) inhibits switching. However, cells must maintain homeostasis in switching to navigate within environments of different viscosities. The mechanism by which the cell maintains optimal chemotactic function under varying loads is not understood. Here, we show that the flagellar motor allosterically controls the binding affinity of the chemotaxis response regulator, CheY-P, to the flagellar switch complex by modulating the mechanical forces acting on the rotor. Mechanosensitive CheY-P binding compensates for the load-induced loss of switching by precisely adapting the switch response to a mechanical stimulus. The interplay between mechanical forces and CheY-P binding tunes the chemotactic function to match the load. This adaptive response of the chemotaxis output to mechanical stimuli resembles the proprioceptive feedback in the neuromuscular systems of insects and vertebrates. |
format | Online Article Text |
id | pubmed-8440544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84405442021-10-04 Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor Antani, Jyot D. Gupta, Rachit Lee, Annie H. Rhee, Kathy Y. Manson, Michael D. Lele, Pushkar P. Nat Commun Article Reversible switching of the bacterial flagellar motor between clockwise (CW) and counterclockwise (CCW) rotation is necessary for chemotaxis, which enables cells to swim towards favorable chemical habitats. Increase in the viscous resistance to the rotation of the motor (mechanical load) inhibits switching. However, cells must maintain homeostasis in switching to navigate within environments of different viscosities. The mechanism by which the cell maintains optimal chemotactic function under varying loads is not understood. Here, we show that the flagellar motor allosterically controls the binding affinity of the chemotaxis response regulator, CheY-P, to the flagellar switch complex by modulating the mechanical forces acting on the rotor. Mechanosensitive CheY-P binding compensates for the load-induced loss of switching by precisely adapting the switch response to a mechanical stimulus. The interplay between mechanical forces and CheY-P binding tunes the chemotactic function to match the load. This adaptive response of the chemotaxis output to mechanical stimuli resembles the proprioceptive feedback in the neuromuscular systems of insects and vertebrates. Nature Publishing Group UK 2021-09-14 /pmc/articles/PMC8440544/ /pubmed/34521846 http://dx.doi.org/10.1038/s41467-021-25774-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Antani, Jyot D. Gupta, Rachit Lee, Annie H. Rhee, Kathy Y. Manson, Michael D. Lele, Pushkar P. Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor |
title | Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor |
title_full | Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor |
title_fullStr | Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor |
title_full_unstemmed | Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor |
title_short | Mechanosensitive recruitment of stator units promotes binding of the response regulator CheY-P to the flagellar motor |
title_sort | mechanosensitive recruitment of stator units promotes binding of the response regulator chey-p to the flagellar motor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440544/ https://www.ncbi.nlm.nih.gov/pubmed/34521846 http://dx.doi.org/10.1038/s41467-021-25774-2 |
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