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Linking path and filament persistence lengths of microtubules gliding over kinesin
Microtubules and kinesin motor proteins are involved in intracellular transports in living cells. Such intracellular material transport systems can be reconstructed for utilisation in synthetic environments, and they are called molecular shuttles driven by kinesin motors. The performance of the mole...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866476/ https://www.ncbi.nlm.nih.gov/pubmed/35197505 http://dx.doi.org/10.1038/s41598-022-06941-x |
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author | Sweet, May Kang’iri, Samuel Macharia Nitta, Takahiro |
author_facet | Sweet, May Kang’iri, Samuel Macharia Nitta, Takahiro |
author_sort | Sweet, May |
collection | PubMed |
description | Microtubules and kinesin motor proteins are involved in intracellular transports in living cells. Such intracellular material transport systems can be reconstructed for utilisation in synthetic environments, and they are called molecular shuttles driven by kinesin motors. The performance of the molecular shuttles depends on the nature of their trajectories, which can be characterized by the path persistence length of microtubules. It has been theoretically predicted that the path persistence length should be equal to the filament persistence length of the microtubules, where the filament persistence length is a measure of microtubule flexural stiffness. However, previous experiments have shown that there is a significant discrepancy between the path and filament persistence lengths. Here, we showed how this discrepancy arises by using computer simulation. By simulating molecular shuttle movements under external forces, the discrepancy between the path and filament persistence lengths was reproduced as observed in experiments. Our close investigations of molecular shuttle movements revealed that the part of the microtubules bent due to the external force was extended more than it was assumed in the theory. By considering the extended length, we could elucidate the discrepancy. The insights obtained here are expected to lead to better control of molecular shuttle movements. |
format | Online Article Text |
id | pubmed-8866476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88664762022-02-25 Linking path and filament persistence lengths of microtubules gliding over kinesin Sweet, May Kang’iri, Samuel Macharia Nitta, Takahiro Sci Rep Article Microtubules and kinesin motor proteins are involved in intracellular transports in living cells. Such intracellular material transport systems can be reconstructed for utilisation in synthetic environments, and they are called molecular shuttles driven by kinesin motors. The performance of the molecular shuttles depends on the nature of their trajectories, which can be characterized by the path persistence length of microtubules. It has been theoretically predicted that the path persistence length should be equal to the filament persistence length of the microtubules, where the filament persistence length is a measure of microtubule flexural stiffness. However, previous experiments have shown that there is a significant discrepancy between the path and filament persistence lengths. Here, we showed how this discrepancy arises by using computer simulation. By simulating molecular shuttle movements under external forces, the discrepancy between the path and filament persistence lengths was reproduced as observed in experiments. Our close investigations of molecular shuttle movements revealed that the part of the microtubules bent due to the external force was extended more than it was assumed in the theory. By considering the extended length, we could elucidate the discrepancy. The insights obtained here are expected to lead to better control of molecular shuttle movements. Nature Publishing Group UK 2022-02-23 /pmc/articles/PMC8866476/ /pubmed/35197505 http://dx.doi.org/10.1038/s41598-022-06941-x Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Sweet, May Kang’iri, Samuel Macharia Nitta, Takahiro Linking path and filament persistence lengths of microtubules gliding over kinesin |
title | Linking path and filament persistence lengths of microtubules gliding over kinesin |
title_full | Linking path and filament persistence lengths of microtubules gliding over kinesin |
title_fullStr | Linking path and filament persistence lengths of microtubules gliding over kinesin |
title_full_unstemmed | Linking path and filament persistence lengths of microtubules gliding over kinesin |
title_short | Linking path and filament persistence lengths of microtubules gliding over kinesin |
title_sort | linking path and filament persistence lengths of microtubules gliding over kinesin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866476/ https://www.ncbi.nlm.nih.gov/pubmed/35197505 http://dx.doi.org/10.1038/s41598-022-06941-x |
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