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Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors

The dynamic organization of signaling cascades inside primary cilia is key to signal propagation. Yet little is known about the dynamics of ciliary membrane proteins besides a possible role for motor-driven Intraflagellar Transport (IFT). To characterize these dynamics, we imaged single molecules of...

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Detalles Bibliográficos
Autores principales: Ye, Fan, Breslow, David K, Koslover, Elena F, Spakowitz, Andrew J, Nelson, W James, Nachury, Maxence V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736543/
https://www.ncbi.nlm.nih.gov/pubmed/23930224
http://dx.doi.org/10.7554/eLife.00654
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author Ye, Fan
Breslow, David K
Koslover, Elena F
Spakowitz, Andrew J
Nelson, W James
Nachury, Maxence V
author_facet Ye, Fan
Breslow, David K
Koslover, Elena F
Spakowitz, Andrew J
Nelson, W James
Nachury, Maxence V
author_sort Ye, Fan
collection PubMed
description The dynamic organization of signaling cascades inside primary cilia is key to signal propagation. Yet little is known about the dynamics of ciliary membrane proteins besides a possible role for motor-driven Intraflagellar Transport (IFT). To characterize these dynamics, we imaged single molecules of Somatostatin Receptor 3 (SSTR3, a GPCR) and Smoothened (Smo, a Hedgehog signal transducer) in the ciliary membrane. While IFT trains moved processively from one end of the cilium to the other, single SSTR3 and Smo underwent mostly diffusive behavior interspersed with short periods of directional movements. Statistical subtraction of instant velocities revealed that SSTR3 and Smo spent less than a third of their time undergoing active transport. Finally, SSTR3 and IFT movements could be uncoupled by perturbing either membrane protein diffusion or active transport. Thus ciliary membrane proteins move predominantly by diffusion, and attachment to IFT trains is transient and stochastic rather than processive or spatially determined. DOI: http://dx.doi.org/10.7554/eLife.00654.001
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spelling pubmed-37365432013-08-08 Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors Ye, Fan Breslow, David K Koslover, Elena F Spakowitz, Andrew J Nelson, W James Nachury, Maxence V eLife Cell Biology The dynamic organization of signaling cascades inside primary cilia is key to signal propagation. Yet little is known about the dynamics of ciliary membrane proteins besides a possible role for motor-driven Intraflagellar Transport (IFT). To characterize these dynamics, we imaged single molecules of Somatostatin Receptor 3 (SSTR3, a GPCR) and Smoothened (Smo, a Hedgehog signal transducer) in the ciliary membrane. While IFT trains moved processively from one end of the cilium to the other, single SSTR3 and Smo underwent mostly diffusive behavior interspersed with short periods of directional movements. Statistical subtraction of instant velocities revealed that SSTR3 and Smo spent less than a third of their time undergoing active transport. Finally, SSTR3 and IFT movements could be uncoupled by perturbing either membrane protein diffusion or active transport. Thus ciliary membrane proteins move predominantly by diffusion, and attachment to IFT trains is transient and stochastic rather than processive or spatially determined. DOI: http://dx.doi.org/10.7554/eLife.00654.001 eLife Sciences Publications, Ltd 2013-08-06 /pmc/articles/PMC3736543/ /pubmed/23930224 http://dx.doi.org/10.7554/eLife.00654 Text en Copyright © 2013, Ye et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Ye, Fan
Breslow, David K
Koslover, Elena F
Spakowitz, Andrew J
Nelson, W James
Nachury, Maxence V
Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
title Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
title_full Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
title_fullStr Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
title_full_unstemmed Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
title_short Single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
title_sort single molecule imaging reveals a major role for diffusion in the exploration of ciliary space by signaling receptors
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3736543/
https://www.ncbi.nlm.nih.gov/pubmed/23930224
http://dx.doi.org/10.7554/eLife.00654
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