Vesicle budding caused by lysolipid-induced asymmetry stress.


Journal

Biophysical journal
ISSN: 1542-0086
Titre abrégé: Biophys J
Pays: United States
ID NLM: 0370626

Informations de publication

Date de publication:
17 10 2023
Historique:
received: 20 04 2023
revised: 10 08 2023
accepted: 28 08 2023
pmc-release: 17 10 2024
medline: 23 10 2023
pubmed: 31 8 2023
entrez: 31 8 2023
Statut: ppublish

Résumé

Lysolipids such as lauroyl, myristoyl, and palmitoyl lysophosphatidylcholine (LPC) insert into the outer leaflet of liposomes but do not flip to the inner leaflet over many hours. This way, they create asymmetry stress between the intrinsic areas of the two leaflets. We have studied how this stress is relaxed with particular emphasis on the budding and fission of small (diameter 20-30 nm) daughter vesicles (DVs). Asymmetric flow field-flow fractionation was utilized to quantify the extent of budding from large unilamellar vesicles after exposure to LPC. Budding starts at a low threshold of the order of 2 mol% LPC in the outer (and ≈0 mol% LPC in the inner) leaflet. We see reason to assume that the fractional fluorescence intensity from DVs is a good approximation for the fraction of membrane lipid, POPC, transferred into DVs. Accordingly, budding starts with a "budding power" of ≈6 POPC molecules budding off per LPC added, corresponding to a more than 10-fold accumulation of LPC in the outer leaflet of DVs to ≈24 mol%. As long as budding is possible, little strain is built up in the membranes, a claim supported by the lack of changes in limiting fluorescence anisotropy, rotational correlation time, and fluorescence lifetime of symmetrically and asymmetrically inserted TMA-DPH. At physiological osmolarity, budding is typically limited to 20-30% of budded fraction with some batch-to-batch variation, but independent of the LPC species. We hypothesize that the budding limit is determined by the excess area of the liposomes upon preparation, which is then used up upon budding given the larger area-to-volume ratio of smaller liposomes. As the mother vesicles approach ideal spheres, budding must stop. This is qualitatively supported by increased and decreased budding limits of osmotically predeflated and preinflated vesicles, respectively.

Identifiants

pubmed: 37649254
pii: S0006-3495(23)00554-4
doi: 10.1016/j.bpj.2023.08.023
pmc: PMC10598287
pii:
doi:

Substances chimiques

Liposomes 0
Unilamellar Liposomes 0
Membrane Lipids 0
Phosphatidylcholines 0
Lipid Bilayers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4011-4022

Informations de copyright

Copyright © 2023 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

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Auteurs

Lisa Hua (L)

Institute of Pharmaceutical Sciences, University of Freiburg, Freiburg, Germany. Electronic address: lisa.hua@pharmazie.uni-freiburg.de.

Michael Kaiser (M)

Institute of Pharmaceutical Sciences, University of Freiburg, Freiburg, Germany.

Iulia Carabadjac (I)

Institute of Pharmaceutical Sciences, University of Freiburg, Freiburg, Germany.

Annette Meister (A)

ZIK HALOmem and Institute of Biochemistry and Biotechnology, MLU Halle-Wittenberg, Halle, Germany.

Gerd Hause (G)

Biozentrum, MLU Halle-Wittenberg, Halle, Germany.

Heiko Heerklotz (H)

Institute of Pharmaceutical Sciences, University of Freiburg, Freiburg, Germany; Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Canada; Signaling Research Center BIOSS, University of Freiburg, Freiburg, Germany. Electronic address: heiko.heerklotz@pharmazie.uni-freiburg.de.

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Classifications MeSH