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Membrane mediated motor kinetics in microtubule gliding assays

Motor-based transport mechanisms are critical for a wide range of eukaryotic cell functions, including the transport of vesicle cargos over long distances. Our understanding of the factors that control and regulate motors when bound to a lipid substrate is however incomplete. We used microtubule gli...

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Autores principales: Lopes, Joseph, Quint, David A., Chapman, Dail E., Xu, Melissa, Gopinathan, Ajay, Hirst, Linda S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610617/
https://www.ncbi.nlm.nih.gov/pubmed/31270348
http://dx.doi.org/10.1038/s41598-019-45847-z
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author Lopes, Joseph
Quint, David A.
Chapman, Dail E.
Xu, Melissa
Gopinathan, Ajay
Hirst, Linda S.
author_facet Lopes, Joseph
Quint, David A.
Chapman, Dail E.
Xu, Melissa
Gopinathan, Ajay
Hirst, Linda S.
author_sort Lopes, Joseph
collection PubMed
description Motor-based transport mechanisms are critical for a wide range of eukaryotic cell functions, including the transport of vesicle cargos over long distances. Our understanding of the factors that control and regulate motors when bound to a lipid substrate is however incomplete. We used microtubule gliding assays on a lipid bilayer substrate to investigate the role of membrane diffusion in kinesin-1 on/off binding kinetics and thereby transport velocity. Fluorescence imaging experiments demonstrate motor clustering on single microtubules due to membrane diffusion in the absence of ATP, followed by rapid ATP-induced dissociation during gliding. Our experimental data combined with analytical modeling show that the on/off binding kinetics of the motors are impacted by diffusion and, as a consequence, both the effective binding and unbinding rates for motors are much lower than the expected bare rates. Our results suggest that motor diffusion in the membrane can play a significant role in transport by impacting motor kinetics and can therefore function as a regulator of intracellular transport dynamics.
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spelling pubmed-66106172019-07-15 Membrane mediated motor kinetics in microtubule gliding assays Lopes, Joseph Quint, David A. Chapman, Dail E. Xu, Melissa Gopinathan, Ajay Hirst, Linda S. Sci Rep Article Motor-based transport mechanisms are critical for a wide range of eukaryotic cell functions, including the transport of vesicle cargos over long distances. Our understanding of the factors that control and regulate motors when bound to a lipid substrate is however incomplete. We used microtubule gliding assays on a lipid bilayer substrate to investigate the role of membrane diffusion in kinesin-1 on/off binding kinetics and thereby transport velocity. Fluorescence imaging experiments demonstrate motor clustering on single microtubules due to membrane diffusion in the absence of ATP, followed by rapid ATP-induced dissociation during gliding. Our experimental data combined with analytical modeling show that the on/off binding kinetics of the motors are impacted by diffusion and, as a consequence, both the effective binding and unbinding rates for motors are much lower than the expected bare rates. Our results suggest that motor diffusion in the membrane can play a significant role in transport by impacting motor kinetics and can therefore function as a regulator of intracellular transport dynamics. Nature Publishing Group UK 2019-07-03 /pmc/articles/PMC6610617/ /pubmed/31270348 http://dx.doi.org/10.1038/s41598-019-45847-z Text en © The Author(s) 2019 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/.
spellingShingle Article
Lopes, Joseph
Quint, David A.
Chapman, Dail E.
Xu, Melissa
Gopinathan, Ajay
Hirst, Linda S.
Membrane mediated motor kinetics in microtubule gliding assays
title Membrane mediated motor kinetics in microtubule gliding assays
title_full Membrane mediated motor kinetics in microtubule gliding assays
title_fullStr Membrane mediated motor kinetics in microtubule gliding assays
title_full_unstemmed Membrane mediated motor kinetics in microtubule gliding assays
title_short Membrane mediated motor kinetics in microtubule gliding assays
title_sort membrane mediated motor kinetics in microtubule gliding assays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610617/
https://www.ncbi.nlm.nih.gov/pubmed/31270348
http://dx.doi.org/10.1038/s41598-019-45847-z
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