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Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model
Axonal motor driven cargo utilizes the microtubule cytoskeleton in order to direct cargo, such as synaptic vesicle precursors (SVP), to where they are needed. This transport requires vesicles to travel up to microns in distance. It has recently been observed that finite microtubule lengths can act a...
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/PMC7873188/ https://www.ncbi.nlm.nih.gov/pubmed/33564025 http://dx.doi.org/10.1038/s41598-021-82836-7 |
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author | Gramlich, M. W. Balseiro-Gómez, S. Tabei, S. M. Ali Parkes, M. Yogev, S. |
author_facet | Gramlich, M. W. Balseiro-Gómez, S. Tabei, S. M. Ali Parkes, M. Yogev, S. |
author_sort | Gramlich, M. W. |
collection | PubMed |
description | Axonal motor driven cargo utilizes the microtubule cytoskeleton in order to direct cargo, such as synaptic vesicle precursors (SVP), to where they are needed. This transport requires vesicles to travel up to microns in distance. It has recently been observed that finite microtubule lengths can act as roadblocks inhibiting SVP and increasing the time required for transport. SVPs reach the end of a microtubule and pause until they can navigate to a neighboring microtubule in order to continue transport. The mechanism(s) by which axonal SVPs navigate the end of a microtubule in order to continue mobility is unknown. In this manuscript we model experimentally observed vesicle pausing at microtubule ends in C. elegans. We show that a single rate-constant model reproduces the time SVPs pause at MT-ends. This model is based on the time an SVP must detach from its current microtubule and re-attach to a neighboring microtubule. We show that vesicle pause times are different for anterograde and retrograde motion, suggesting that vesicles utilize different proteins at plus and minus end sites. Last, we show that vesicles do not likely utilize a tug-of-war like mechanism and reverse direction in order to navigate microtubule ends. |
format | Online Article Text |
id | pubmed-7873188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78731882021-02-11 Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model Gramlich, M. W. Balseiro-Gómez, S. Tabei, S. M. Ali Parkes, M. Yogev, S. Sci Rep Article Axonal motor driven cargo utilizes the microtubule cytoskeleton in order to direct cargo, such as synaptic vesicle precursors (SVP), to where they are needed. This transport requires vesicles to travel up to microns in distance. It has recently been observed that finite microtubule lengths can act as roadblocks inhibiting SVP and increasing the time required for transport. SVPs reach the end of a microtubule and pause until they can navigate to a neighboring microtubule in order to continue transport. The mechanism(s) by which axonal SVPs navigate the end of a microtubule in order to continue mobility is unknown. In this manuscript we model experimentally observed vesicle pausing at microtubule ends in C. elegans. We show that a single rate-constant model reproduces the time SVPs pause at MT-ends. This model is based on the time an SVP must detach from its current microtubule and re-attach to a neighboring microtubule. We show that vesicle pause times are different for anterograde and retrograde motion, suggesting that vesicles utilize different proteins at plus and minus end sites. Last, we show that vesicles do not likely utilize a tug-of-war like mechanism and reverse direction in order to navigate microtubule ends. Nature Publishing Group UK 2021-02-09 /pmc/articles/PMC7873188/ /pubmed/33564025 http://dx.doi.org/10.1038/s41598-021-82836-7 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Gramlich, M. W. Balseiro-Gómez, S. Tabei, S. M. Ali Parkes, M. Yogev, S. Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model |
title | Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model |
title_full | Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model |
title_fullStr | Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model |
title_full_unstemmed | Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model |
title_short | Distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model |
title_sort | distinguishing synaptic vesicle precursor navigation of microtubule ends with a single rate constant model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7873188/ https://www.ncbi.nlm.nih.gov/pubmed/33564025 http://dx.doi.org/10.1038/s41598-021-82836-7 |
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