English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Superelasticity of plasma- and synthetic membranes resulting from coupling of membrane asymmetry, curvature, and lipid sorting

Steinkühler, J., Fonda, P., Bhatia, T., Zhao, Z., Leomil, F., Lipowsky, R., et al. (2021). Superelasticity of plasma- and synthetic membranes resulting from coupling of membrane asymmetry, curvature, and lipid sorting. Advanced Science, 8(21): 2102109. doi:10.1002/advs.202102109.

Item is

Files

show Files
hide Files
:
Article.pdf (Publisher version), 4MB
Name:
Article.pdf
Description:
-
OA-Status:
Gold
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-
:
Preprint.pdf (Any fulltext), 3MB
Name:
Preprint.pdf
Description:
-
OA-Status:
Not specified
Visibility:
Public
MIME-Type / Checksum:
application/pdf / [MD5]
Technical Metadata:
Copyright Date:
-
Copyright Info:
-

Locators

show

Creators

show
hide
 Creators:
Steinkühler, Jan1, Author           
Fonda, Piermarco2, Author           
Bhatia, Tripta1, Author           
Zhao, Ziliang1, Author           
Leomil, Fernanda1, Author           
Lipowsky, Reinhard2, Author           
Dimova, Rumiana1, Author           
Affiliations:
1Rumiana Dimova, Theorie & Bio-Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863328              
2Reinhard Lipowsky, Theorie & Bio-Systeme, Max Planck Institute of Colloids and Interfaces, Max Planck Society, ou_1863327              

Content

show
hide
Free keywords: giant plasma membrane vesicles; lipid domains; micropipette; plasma membrane, spontaneous curvature; superelasticity; synthetic biology
 Abstract: Biological cells are contained by a fluid lipid bilayer (plasma membrane, PM) that allows for large deformations, often exceeding 50% of the apparent initial PM area. Isolated lipids self-organize into membranes, but are prone to rupture at small (<2–4%) area strains, which limits progress for synthetic reconstitution of cellular features. Here, it is shown that by preserving PM structure and composition during isolation from cells, vesicles with cell-like elasticity can be obtained. It is found that these plasma membrane vesicles store significant area in the form of nanotubes in their lumen. These act as lipid reservoirs and are recruited by mechanical tension applied to the outer vesicle membrane. Both in experiment and theory, it is shown that a “superelastic” response emerges from the interplay of lipid domains and membrane curvature. This finding allows for bottom-up engineering of synthetic biomaterials that appear one magnitude softer and with threefold larger deformability than conventional lipid vesicles. These results open a path toward designing superelastic synthetic cells possessing the inherent mechanics of biological cells.

Details

show
hide
Language(s): eng - English
 Dates: 2021-09-262021
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Advanced Science
  Other : Adv. Sci.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Weinheim : Wiley-VCH
Pages: - Volume / Issue: 8 (21) Sequence Number: 2102109 Start / End Page: - Identifier: ISSN: 2198-3844

Source 2

show
hide
Title: bioRxiv
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: Cold Spring Harbor : Cold Spring Harbor Laboratory
Pages: - Volume / Issue: - Sequence Number: 198333 Start / End Page: - Identifier: ZDB: 2766415-6