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Kinetic properties and small-molecule inhibition of human myosin-6
Myosin-6 is an actin-based motor protein that moves its cargo towards the minus-end of actin filaments. Mutations in the gene encoding the myosin-6 heavy chain and changes in the cellular abundance of the protein have been linked to hypertrophic cardiomyopathy, neurodegenerative diseases, and cancer...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science B.V
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527664/ https://www.ncbi.nlm.nih.gov/pubmed/22884421 http://dx.doi.org/10.1016/j.febslet.2012.07.014 |
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author | Heissler, Sarah M. Selvadurai, Jayashankar Bond, Lisa M. Fedorov, Roman Kendrick-Jones, John Buss, Folma Manstein, Dietmar J. |
author_facet | Heissler, Sarah M. Selvadurai, Jayashankar Bond, Lisa M. Fedorov, Roman Kendrick-Jones, John Buss, Folma Manstein, Dietmar J. |
author_sort | Heissler, Sarah M. |
collection | PubMed |
description | Myosin-6 is an actin-based motor protein that moves its cargo towards the minus-end of actin filaments. Mutations in the gene encoding the myosin-6 heavy chain and changes in the cellular abundance of the protein have been linked to hypertrophic cardiomyopathy, neurodegenerative diseases, and cancer. Here, we present a detailed kinetic characterization of the human myosin-6 motor domain, describe the effect of 2,4,6-triiodophenol on the interaction of myosin-6 with F-actin and nucleotides, and show how addition of the drug reduces the number of myosin-6-dependent vesicle fusion events at the plasma membrane during constitutive secretion. |
format | Online Article Text |
id | pubmed-3527664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier Science B.V |
record_format | MEDLINE/PubMed |
spelling | pubmed-35276642012-12-22 Kinetic properties and small-molecule inhibition of human myosin-6 Heissler, Sarah M. Selvadurai, Jayashankar Bond, Lisa M. Fedorov, Roman Kendrick-Jones, John Buss, Folma Manstein, Dietmar J. FEBS Lett Article Myosin-6 is an actin-based motor protein that moves its cargo towards the minus-end of actin filaments. Mutations in the gene encoding the myosin-6 heavy chain and changes in the cellular abundance of the protein have been linked to hypertrophic cardiomyopathy, neurodegenerative diseases, and cancer. Here, we present a detailed kinetic characterization of the human myosin-6 motor domain, describe the effect of 2,4,6-triiodophenol on the interaction of myosin-6 with F-actin and nucleotides, and show how addition of the drug reduces the number of myosin-6-dependent vesicle fusion events at the plasma membrane during constitutive secretion. Elsevier Science B.V 2012-09-21 /pmc/articles/PMC3527664/ /pubmed/22884421 http://dx.doi.org/10.1016/j.febslet.2012.07.014 Text en © 2012 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license |
spellingShingle | Article Heissler, Sarah M. Selvadurai, Jayashankar Bond, Lisa M. Fedorov, Roman Kendrick-Jones, John Buss, Folma Manstein, Dietmar J. Kinetic properties and small-molecule inhibition of human myosin-6 |
title | Kinetic properties and small-molecule inhibition of human myosin-6 |
title_full | Kinetic properties and small-molecule inhibition of human myosin-6 |
title_fullStr | Kinetic properties and small-molecule inhibition of human myosin-6 |
title_full_unstemmed | Kinetic properties and small-molecule inhibition of human myosin-6 |
title_short | Kinetic properties and small-molecule inhibition of human myosin-6 |
title_sort | kinetic properties and small-molecule inhibition of human myosin-6 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527664/ https://www.ncbi.nlm.nih.gov/pubmed/22884421 http://dx.doi.org/10.1016/j.febslet.2012.07.014 |
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