Membrane nanotubes transform into double-membrane sheets at condensate droplets.

condensate interface double-membrane sheet giant unilamellar vesicles (GUV) stimulated emission depletion (STED) tube-to-sheet transformation

Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
25 Jun 2024
Historique:
medline: 20 6 2024
pubmed: 20 6 2024
entrez: 20 6 2024
Statut: ppublish

Résumé

Cellular membranes exhibit a multitude of highly curved morphologies such as buds, nanotubes, cisterna-like sheets defining the outlines of organelles. Here, we mimic cell compartmentation using an aqueous two-phase system of dextran and poly(ethylene glycol) encapsulated in giant vesicles. Upon osmotic deflation, the vesicle membrane forms nanotubes, which undergo surprising morphological transformations at the liquid-liquid interfaces inside the vesicles. At these interfaces, the nanotubes transform into cisterna-like double-membrane sheets (DMS) connected to the mother vesicle via short membrane necks. Using super-resolution (stimulated emission depletion) microscopy and theoretical considerations, we construct a morphology diagram predicting the tube-to-sheet transformation, which is driven by a decrease in the free energy. Nanotube knots can prohibit the tube-to-sheet transformation by blocking water influx into the tubes. Because both nanotubes and DMSs are frequently formed by cellular membranes, understanding the formation and transformation between these membrane morphologies provides insight into the origin and evolution of cellular organelles.

Identifiants

pubmed: 38900795
doi: 10.1073/pnas.2321579121
doi:

Substances chimiques

Polyethylene Glycols 3WJQ0SDW1A
Dextrans 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2321579121

Subventions

Organisme : Bundesministerium für Bildung und Forschung (BMBF)
ID : MaxSynBio
Organisme : Thueringer Aufbaubank
ID : SARSRapid 2020-FGR-0052
Organisme : Deutsche Forschungsgemeinschaft (DFG)
ID : project number 316213987 - SFB 1278

Déclaration de conflit d'intérêts

Competing interests statement:The authors declare no competing interest.

Auteurs

Ziliang Zhao (Z)

Max Planck Institute of Colloids and Interfaces, Potsdam 14476, Germany.
Leibniz Institute of Photonic Technology e.V., Jena 07745, Germany.
Institute of Applied Optics and Biophysics, Friedrich-Schiller-University Jena, Jena 07743, Germany.

Vahid Satarifard (V)

Max Planck Institute of Colloids and Interfaces, Potsdam 14476, Germany.
Yale Institute for Network Science, Yale University, New Haven, CT 06520.

Reinhard Lipowsky (R)

Max Planck Institute of Colloids and Interfaces, Potsdam 14476, Germany.

Rumiana Dimova (R)

Max Planck Institute of Colloids and Interfaces, Potsdam 14476, Germany.

Articles similaires

Humans Animals Adherens Junctions Intercellular Junctions Tight Junctions
1.00
Plasmodesmata Endoplasmic Reticulum Arabidopsis Cytokinesis Arabidopsis Proteins
Angiotensin-Converting Enzyme 2 Humans SARS-CoV-2 Spike Glycoprotein, Coronavirus Receptors, Virus

Molecular probes for tracking lipid droplet membrane dynamics.

Lingxiu Kong, Qingjie Bai, Cuicui Li et al.
1.00
Lipid Droplets Molecular Probes Humans Membrane Proteins Animals

Classifications MeSH