Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport
Dynein-dependent transport of organelles from the axon terminals to the cell bodies is essential to the survival and function of neurons. However, quantitative knowledge of dyneins on axonal organelles and their collective function during this long-distance transport is lacking because current techn...
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sg-ntu-dr.10356-815842023-12-29T06:52:30Z Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport Cui, Bianxiao Chowdary, Praveen D. Che, Daphne L. Kaplan, Luke Chen, Ou Pu, Kanyi Bawendi, Moungi School of Chemical and Biomedical Engineering Chemical and Biomedical Engineering Dynein-dependent transport of organelles from the axon terminals to the cell bodies is essential to the survival and function of neurons. However, quantitative knowledge of dyneins on axonal organelles and their collective function during this long-distance transport is lacking because current technologies to do such measurements are not applicable to neurons. Here, we report a new method termed nanoparticle-assisted optical tethering of endosomes (NOTE) that made it possible to study the cooperative mechanics of dyneins on retrograde axonal endosomes in live neurons. In this method, the opposing force from an elastic tether causes the endosomes to gradually stall under load and detach with a recoil velocity proportional to the dynein forces. These recoil velocities reveal that the axonal endosomes, despite their small size, can recruit up to 7 dyneins that function as independent mechanical units stochastically sharing load, which is vital for robust retrograde axonal transport. This study shows that NOTE, which relies on controlled generation of reactive oxygen species, is a viable method to manipulate small cellular cargos that are beyond the reach of current technology. Published version 2016-01-05T09:22:00Z 2019-12-06T14:34:18Z 2016-01-05T09:22:00Z 2019-12-06T14:34:18Z 2015 Journal Article Chowdary, P. D., Che, D. L., Kaplan, L., Chen, O., Pu, K., Bawendi, M., et al. (2015). Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport. Scientific Reports, 5, 18059-. 2045-2322 https://hdl.handle.net/10356/81584 http://hdl.handle.net/10220/39577 10.1038/srep18059 26656461 en Scientific Reports 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/ 11 p. application/pdf |
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Chemical and Biomedical Engineering Cui, Bianxiao Chowdary, Praveen D. Che, Daphne L. Kaplan, Luke Chen, Ou Pu, Kanyi Bawendi, Moungi Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport |
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Dynein-dependent transport of organelles from the axon terminals to the cell bodies is essential to the survival and function of neurons. However, quantitative knowledge of dyneins on axonal organelles and their collective function during this long-distance transport is lacking because current technologies to do such measurements are not applicable to neurons. Here, we report a new method termed nanoparticle-assisted optical tethering of endosomes (NOTE) that made it possible to study the cooperative mechanics of dyneins on retrograde axonal endosomes in live neurons. In this method, the opposing force from an elastic tether causes the endosomes to gradually stall under load and detach with a recoil velocity proportional to the dynein forces. These recoil velocities reveal that the axonal endosomes, despite their small size, can recruit up to 7 dyneins that function as independent mechanical units stochastically sharing load, which is vital for robust retrograde axonal transport. This study shows that NOTE, which relies on controlled generation of reactive oxygen species, is a viable method to manipulate small cellular cargos that are beyond the reach of current technology. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Cui, Bianxiao Chowdary, Praveen D. Che, Daphne L. Kaplan, Luke Chen, Ou Pu, Kanyi Bawendi, Moungi |
format |
Article |
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Cui, Bianxiao Chowdary, Praveen D. Che, Daphne L. Kaplan, Luke Chen, Ou Pu, Kanyi Bawendi, Moungi |
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Cui, Bianxiao |
title |
Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport |
title_short |
Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport |
title_full |
Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport |
title_fullStr |
Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport |
title_full_unstemmed |
Nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport |
title_sort |
nanoparticle-assisted optical tethering of endosomes reveals the cooperative function of dyneins in retrograde axonal transport |
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2016 |
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https://hdl.handle.net/10356/81584 http://hdl.handle.net/10220/39577 |
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1787136772119986176 |