Cargando…

Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells

[Image: see text] Molecular motors are pivotal for intracellular transport as well as cell motility and have great potential to be put to use outside cells. Here, we exploit engineered motor proteins in combination with self-assembly of actin filaments to actively pull lipid nanotubes from giant uni...

Descripción completa

Detalles Bibliográficos
Autores principales: Jahnke, Kevin, Maurer, Stefan J., Weber, Cornelia, Bücher, Jochen Estebano Hernandez, Schoenit, Andreas, D’Este, Elisa, Cavalcanti-Adam, Elisabetta Ada, Göpfrich, Kerstin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832490/
https://www.ncbi.nlm.nih.gov/pubmed/35089720
http://dx.doi.org/10.1021/acs.nanolett.1c04254
_version_ 1784648731305443328
author Jahnke, Kevin
Maurer, Stefan J.
Weber, Cornelia
Bücher, Jochen Estebano Hernandez
Schoenit, Andreas
D’Este, Elisa
Cavalcanti-Adam, Elisabetta Ada
Göpfrich, Kerstin
author_facet Jahnke, Kevin
Maurer, Stefan J.
Weber, Cornelia
Bücher, Jochen Estebano Hernandez
Schoenit, Andreas
D’Este, Elisa
Cavalcanti-Adam, Elisabetta Ada
Göpfrich, Kerstin
author_sort Jahnke, Kevin
collection PubMed
description [Image: see text] Molecular motors are pivotal for intracellular transport as well as cell motility and have great potential to be put to use outside cells. Here, we exploit engineered motor proteins in combination with self-assembly of actin filaments to actively pull lipid nanotubes from giant unilamellar vesicles (GUVs). In particular, actin filaments are bound to the outer GUV membrane and the GUVs are seeded on a heavy meromyosin-coated substrate. Upon addition of ATP, hollow lipid nanotubes with a length of tens of micrometer are pulled from single GUVs due to the motor activity. We employ the same mechanism to pull lipid nanotubes from different types of cells. We find that the length and number of nanotubes critically depends on the cell type, whereby suspension cells form bigger networks than adherent cells. This suggests that molecular machines can be used to exert forces on living cells to probe membrane-to-cortex attachment.
format Online
Article
Text
id pubmed-8832490
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-88324902022-02-11 Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells Jahnke, Kevin Maurer, Stefan J. Weber, Cornelia Bücher, Jochen Estebano Hernandez Schoenit, Andreas D’Este, Elisa Cavalcanti-Adam, Elisabetta Ada Göpfrich, Kerstin Nano Lett [Image: see text] Molecular motors are pivotal for intracellular transport as well as cell motility and have great potential to be put to use outside cells. Here, we exploit engineered motor proteins in combination with self-assembly of actin filaments to actively pull lipid nanotubes from giant unilamellar vesicles (GUVs). In particular, actin filaments are bound to the outer GUV membrane and the GUVs are seeded on a heavy meromyosin-coated substrate. Upon addition of ATP, hollow lipid nanotubes with a length of tens of micrometer are pulled from single GUVs due to the motor activity. We employ the same mechanism to pull lipid nanotubes from different types of cells. We find that the length and number of nanotubes critically depends on the cell type, whereby suspension cells form bigger networks than adherent cells. This suggests that molecular machines can be used to exert forces on living cells to probe membrane-to-cortex attachment. American Chemical Society 2022-01-28 2022-02-09 /pmc/articles/PMC8832490/ /pubmed/35089720 http://dx.doi.org/10.1021/acs.nanolett.1c04254 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Jahnke, Kevin
Maurer, Stefan J.
Weber, Cornelia
Bücher, Jochen Estebano Hernandez
Schoenit, Andreas
D’Este, Elisa
Cavalcanti-Adam, Elisabetta Ada
Göpfrich, Kerstin
Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells
title Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells
title_full Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells
title_fullStr Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells
title_full_unstemmed Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells
title_short Actomyosin-Assisted Pulling of Lipid Nanotubes from Lipid Vesicles and Cells
title_sort actomyosin-assisted pulling of lipid nanotubes from lipid vesicles and cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8832490/
https://www.ncbi.nlm.nih.gov/pubmed/35089720
http://dx.doi.org/10.1021/acs.nanolett.1c04254
work_keys_str_mv AT jahnkekevin actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells
AT maurerstefanj actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells
AT webercornelia actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells
AT bucherjochenestebanohernandez actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells
AT schoenitandreas actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells
AT desteelisa actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells
AT cavalcantiadamelisabettaada actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells
AT gopfrichkerstin actomyosinassistedpullingoflipidnanotubesfromlipidvesiclesandcells