Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting

Curvature-mediating proteins are known to induce specific membrane shapes, but whether motorprotein-lipid interactions remodel membranes too remains unclear. Here authors show that curvature-dependent lipid interactions of myosin-VI remodel the membrane geometry into dynamic spatial patterns.

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Autores principales: Benoit Rogez, Laeschkir Würthner, Anastasiia B. Petrova, Felix B. Zierhut, Dario Saczko-Brack, Maria-Ana Huergo, Christopher Batters, Erwin Frey, Claudia Veigel
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Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/da69c820db8b4ae1b1ef6a2cc0804e10
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spelling oai:doaj.org-article:da69c820db8b4ae1b1ef6a2cc0804e102021-12-02T16:57:52ZReconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting10.1038/s41467-019-11268-92041-1723https://doaj.org/article/da69c820db8b4ae1b1ef6a2cc0804e102019-07-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-11268-9https://doaj.org/toc/2041-1723Curvature-mediating proteins are known to induce specific membrane shapes, but whether motorprotein-lipid interactions remodel membranes too remains unclear. Here authors show that curvature-dependent lipid interactions of myosin-VI remodel the membrane geometry into dynamic spatial patterns.Benoit RogezLaeschkir WürthnerAnastasiia B. PetrovaFelix B. ZierhutDario Saczko-BrackMaria-Ana HuergoChristopher BattersErwin FreyClaudia VeigelNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-11 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Benoit Rogez
Laeschkir Würthner
Anastasiia B. Petrova
Felix B. Zierhut
Dario Saczko-Brack
Maria-Ana Huergo
Christopher Batters
Erwin Frey
Claudia Veigel
Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting
description Curvature-mediating proteins are known to induce specific membrane shapes, but whether motorprotein-lipid interactions remodel membranes too remains unclear. Here authors show that curvature-dependent lipid interactions of myosin-VI remodel the membrane geometry into dynamic spatial patterns.
format article
author Benoit Rogez
Laeschkir Würthner
Anastasiia B. Petrova
Felix B. Zierhut
Dario Saczko-Brack
Maria-Ana Huergo
Christopher Batters
Erwin Frey
Claudia Veigel
author_facet Benoit Rogez
Laeschkir Würthner
Anastasiia B. Petrova
Felix B. Zierhut
Dario Saczko-Brack
Maria-Ana Huergo
Christopher Batters
Erwin Frey
Claudia Veigel
author_sort Benoit Rogez
title Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting
title_short Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting
title_full Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting
title_fullStr Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting
title_full_unstemmed Reconstitution reveals how myosin-VI self-organises to generate a dynamic mechanism of membrane sculpting
title_sort reconstitution reveals how myosin-vi self-organises to generate a dynamic mechanism of membrane sculpting
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/da69c820db8b4ae1b1ef6a2cc0804e10
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