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Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport

Within living cells, the transport of cargo is accomplished by groups of molecular motors. Such collective transport could utilize mechanisms which emerge from inter-motor interactions in ways that are yet to be fully understood. Here we combined experimental measurements of two-kinesin transport wi...

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Autores principales: Ando, David, Mattson, Michelle K., Xu, Jing, Gopinathan, Ajay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248269/
https://www.ncbi.nlm.nih.gov/pubmed/25434968
http://dx.doi.org/10.1038/srep07255
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author Ando, David
Mattson, Michelle K.
Xu, Jing
Gopinathan, Ajay
author_facet Ando, David
Mattson, Michelle K.
Xu, Jing
Gopinathan, Ajay
author_sort Ando, David
collection PubMed
description Within living cells, the transport of cargo is accomplished by groups of molecular motors. Such collective transport could utilize mechanisms which emerge from inter-motor interactions in ways that are yet to be fully understood. Here we combined experimental measurements of two-kinesin transport with a theoretical framework to investigate the functional ramifications of inter-motor interactions on individual motor function and collective cargo transport. In contrast to kinesin's low sidestepping frequency when present as a single motor, with exactly two kinesins per cargo, we observed substantial motion perpendicular to the microtubule. Our model captures a surface-associated mode of kinesin, which is only accessible via inter-motor interference in groups, in which kinesin diffuses along the microtubule surface and rapidly “hops” between protofilaments without dissociating from the microtubule. Critically, each kinesin transitions dynamically between the active stepping mode and this weak surface-associated mode enhancing local exploration of the microtubule surface, possibly enabling cellular cargos to overcome macromolecular crowding and to navigate obstacles along microtubule tracks without sacrificing overall travel distance.
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spelling pubmed-42482692014-12-08 Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport Ando, David Mattson, Michelle K. Xu, Jing Gopinathan, Ajay Sci Rep Article Within living cells, the transport of cargo is accomplished by groups of molecular motors. Such collective transport could utilize mechanisms which emerge from inter-motor interactions in ways that are yet to be fully understood. Here we combined experimental measurements of two-kinesin transport with a theoretical framework to investigate the functional ramifications of inter-motor interactions on individual motor function and collective cargo transport. In contrast to kinesin's low sidestepping frequency when present as a single motor, with exactly two kinesins per cargo, we observed substantial motion perpendicular to the microtubule. Our model captures a surface-associated mode of kinesin, which is only accessible via inter-motor interference in groups, in which kinesin diffuses along the microtubule surface and rapidly “hops” between protofilaments without dissociating from the microtubule. Critically, each kinesin transitions dynamically between the active stepping mode and this weak surface-associated mode enhancing local exploration of the microtubule surface, possibly enabling cellular cargos to overcome macromolecular crowding and to navigate obstacles along microtubule tracks without sacrificing overall travel distance. Nature Publishing Group 2014-12-01 /pmc/articles/PMC4248269/ /pubmed/25434968 http://dx.doi.org/10.1038/srep07255 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Article
Ando, David
Mattson, Michelle K.
Xu, Jing
Gopinathan, Ajay
Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport
title Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport
title_full Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport
title_fullStr Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport
title_full_unstemmed Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport
title_short Cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport
title_sort cooperative protofilament switching emerges from inter-motor interference in multiple-motor transport
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248269/
https://www.ncbi.nlm.nih.gov/pubmed/25434968
http://dx.doi.org/10.1038/srep07255
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