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Examining kinesin processivity within a general gating framework
Kinesin-1 is a dimeric motor that transports cargo along microtubules, taking 8.2-nm steps in a hand-over-hand fashion. The ATP hydrolysis cycles of its two heads are maintained out of phase by a series of gating mechanisms, which lead to processive runs averaging ∼1 μm. A key structural element for...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453223/ https://www.ncbi.nlm.nih.gov/pubmed/25902401 http://dx.doi.org/10.7554/eLife.07403 |
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author | Andreasson, Johan OL Milic, Bojan Chen, Geng-Yuan Guydosh, Nicholas R Hancock, William O Block, Steven M |
author_facet | Andreasson, Johan OL Milic, Bojan Chen, Geng-Yuan Guydosh, Nicholas R Hancock, William O Block, Steven M |
author_sort | Andreasson, Johan OL |
collection | PubMed |
description | Kinesin-1 is a dimeric motor that transports cargo along microtubules, taking 8.2-nm steps in a hand-over-hand fashion. The ATP hydrolysis cycles of its two heads are maintained out of phase by a series of gating mechanisms, which lead to processive runs averaging ∼1 μm. A key structural element for inter-head coordination is the neck linker (NL), which connects the heads to the stalk. To examine the role of the NL in regulating stepping, we investigated NL mutants of various lengths using single-molecule optical trapping and bulk fluorescence approaches in the context of a general framework for gating. Our results show that, although inter-head tension enhances motor velocity, it is crucial neither for inter-head coordination nor for rapid rear-head release. Furthermore, cysteine-light mutants do not produce wild-type motility under load. We conclude that kinesin-1 is primarily front-head gated, and that NL length is tuned to enhance unidirectional processivity and velocity. DOI: http://dx.doi.org/10.7554/eLife.07403.001 |
format | Online Article Text |
id | pubmed-4453223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-44532232015-06-04 Examining kinesin processivity within a general gating framework Andreasson, Johan OL Milic, Bojan Chen, Geng-Yuan Guydosh, Nicholas R Hancock, William O Block, Steven M eLife Biophysics and Structural Biology Kinesin-1 is a dimeric motor that transports cargo along microtubules, taking 8.2-nm steps in a hand-over-hand fashion. The ATP hydrolysis cycles of its two heads are maintained out of phase by a series of gating mechanisms, which lead to processive runs averaging ∼1 μm. A key structural element for inter-head coordination is the neck linker (NL), which connects the heads to the stalk. To examine the role of the NL in regulating stepping, we investigated NL mutants of various lengths using single-molecule optical trapping and bulk fluorescence approaches in the context of a general framework for gating. Our results show that, although inter-head tension enhances motor velocity, it is crucial neither for inter-head coordination nor for rapid rear-head release. Furthermore, cysteine-light mutants do not produce wild-type motility under load. We conclude that kinesin-1 is primarily front-head gated, and that NL length is tuned to enhance unidirectional processivity and velocity. DOI: http://dx.doi.org/10.7554/eLife.07403.001 eLife Sciences Publications, Ltd 2015-04-22 /pmc/articles/PMC4453223/ /pubmed/25902401 http://dx.doi.org/10.7554/eLife.07403 Text en © 2015, Andreasson et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Andreasson, Johan OL Milic, Bojan Chen, Geng-Yuan Guydosh, Nicholas R Hancock, William O Block, Steven M Examining kinesin processivity within a general gating framework |
title | Examining kinesin processivity within a general gating framework |
title_full | Examining kinesin processivity within a general gating framework |
title_fullStr | Examining kinesin processivity within a general gating framework |
title_full_unstemmed | Examining kinesin processivity within a general gating framework |
title_short | Examining kinesin processivity within a general gating framework |
title_sort | examining kinesin processivity within a general gating framework |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4453223/ https://www.ncbi.nlm.nih.gov/pubmed/25902401 http://dx.doi.org/10.7554/eLife.07403 |
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