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Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport
The glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) facilitates fast axonal transport in neurons. However, given that GAPDH does not produce ATP, it is unclear whether glycolysis per se is sufficient to propel vesicles. Although many proteins regulating transport have been identif...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078996/ https://www.ncbi.nlm.nih.gov/pubmed/27775035 http://dx.doi.org/10.1038/ncomms13233 |
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author | Hinckelmann, María-Victoria Virlogeux, Amandine Niehage, Christian Poujol, Christel Choquet, Daniel Hoflack, Bernard Zala, Diana Saudou, Frédéric |
author_facet | Hinckelmann, María-Victoria Virlogeux, Amandine Niehage, Christian Poujol, Christel Choquet, Daniel Hoflack, Bernard Zala, Diana Saudou, Frédéric |
author_sort | Hinckelmann, María-Victoria |
collection | PubMed |
description | The glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) facilitates fast axonal transport in neurons. However, given that GAPDH does not produce ATP, it is unclear whether glycolysis per se is sufficient to propel vesicles. Although many proteins regulating transport have been identified, the molecular composition of transported vesicles in neurons has yet to be fully elucidated. Here we selectively enrich motile vesicles and perform quantitative proteomic analysis. In addition to the expected molecular motors and vesicular proteins, we find an enrichment of all the glycolytic enzymes. Using biochemical approaches and super-resolution microscopy, we observe that most glycolytic enzymes are selectively associated with vesicles and facilitate transport of vesicles in neurons. Finally, we provide evidence that mouse brain vesicles produce ATP from ADP and glucose, and display movement in a reconstituted in vitro transport assay of native vesicles. We conclude that transport of vesicles along microtubules can be autonomous. |
format | Online Article Text |
id | pubmed-5078996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50789962016-11-02 Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport Hinckelmann, María-Victoria Virlogeux, Amandine Niehage, Christian Poujol, Christel Choquet, Daniel Hoflack, Bernard Zala, Diana Saudou, Frédéric Nat Commun Article The glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH) facilitates fast axonal transport in neurons. However, given that GAPDH does not produce ATP, it is unclear whether glycolysis per se is sufficient to propel vesicles. Although many proteins regulating transport have been identified, the molecular composition of transported vesicles in neurons has yet to be fully elucidated. Here we selectively enrich motile vesicles and perform quantitative proteomic analysis. In addition to the expected molecular motors and vesicular proteins, we find an enrichment of all the glycolytic enzymes. Using biochemical approaches and super-resolution microscopy, we observe that most glycolytic enzymes are selectively associated with vesicles and facilitate transport of vesicles in neurons. Finally, we provide evidence that mouse brain vesicles produce ATP from ADP and glucose, and display movement in a reconstituted in vitro transport assay of native vesicles. We conclude that transport of vesicles along microtubules can be autonomous. Nature Publishing Group 2016-10-24 /pmc/articles/PMC5078996/ /pubmed/27775035 http://dx.doi.org/10.1038/ncomms13233 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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 to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hinckelmann, María-Victoria Virlogeux, Amandine Niehage, Christian Poujol, Christel Choquet, Daniel Hoflack, Bernard Zala, Diana Saudou, Frédéric Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport |
title | Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport |
title_full | Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport |
title_fullStr | Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport |
title_full_unstemmed | Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport |
title_short | Self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport |
title_sort | self-propelling vesicles define glycolysis as the minimal energy machinery for neuronal transport |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5078996/ https://www.ncbi.nlm.nih.gov/pubmed/27775035 http://dx.doi.org/10.1038/ncomms13233 |
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