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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...

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Detalles Bibliográficos
Autores principales: Heissler, Sarah M., Selvadurai, Jayashankar, Bond, Lisa M., Fedorov, Roman, Kendrick-Jones, John, Buss, Folma, Manstein, Dietmar J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2012
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.
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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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