Induced asymmetries in membranes.


Journal

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

Informations de publication

Date de publication:
06 06 2023
Historique:
received: 30 06 2022
revised: 11 09 2022
accepted: 01 12 2022
pmc-release: 06 06 2024
medline: 9 6 2023
pubmed: 9 12 2022
entrez: 8 12 2022
Statut: ppublish

Résumé

Lipid asymmetry in plasma membrane of eukaryotes is ubiquitous. The first measurements reported compositional asymmetry: phosphatidylethanolamine and phosphatidylserine are mostly on the cytoplasmic leafet, while phosphatidylcholine and sphingomyelin are mostly on the exoplasmic leaflet. More recent experiments using lipidomics have evidenced the presence of saturation asymmetry between the two leaflets. A question that naturally arises is why such an asymmetry? To complicate matters, it is still largely unknown in which leaflet cholesterol lies. Here, we use chemical potentials to mimic flippase proteins responsible for maintenance of compositional asymmetry in silico. We show that saturation asymmetry naturally arises as a byproduct of phospholipid number asymmetry and sphingomyelin contents, thereby showing that some reported asymmetries may naturally result from others and do not necessarily require being externally driven. We also show that plasmalogen lipids' tendency to be highly unsaturated is also natural. Additionally, we tackle the problem of cholesterol and show that, while it is influenced by all asymmetries, the resulting cholesterol asymmetry tends to be fairly mild.

Identifiants

pubmed: 36476992
pii: S0006-3495(22)03892-9
doi: 10.1016/j.bpj.2022.12.004
pmc: PMC10257082
pii:
doi:

Substances chimiques

Sphingomyelins 0
Phospholipids 0
Cholesterol 97C5T2UQ7J

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2092-2098

Informations de copyright

Copyright © 2022 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Références

Front Cell Dev Biol. 2017 Jan 10;4:155
pubmed: 28119914
J Chem Theory Comput. 2019 Oct 8;15(10):5448-5460
pubmed: 31498621
Traffic. 2018 Oct;19(10):750-760
pubmed: 29896788
J Cell Sci. 2015 Apr 1;128(7):1422-33
pubmed: 25663704
Annu Rev Biochem. 1979;48:47-71
pubmed: 382989
Cell Rep. 2018 Jul 24;24(4):1037-1049
pubmed: 30044971
RSC Adv. 2021 Jun 28;11(37):22677-22682
pubmed: 35480443
Cell. 2015 Apr 23;161(3):581-594
pubmed: 25910209
Biophys J. 2020 Feb 4;118(3):624-642
pubmed: 31954503
Cell. 2010 Jul 9;142(1):158-69
pubmed: 20603021
Soft Matter. 2021 Mar 18;17(10):2742-2752
pubmed: 33533367
Biophys J. 2022 Oct 18;121(20):4001-4018
pubmed: 35927954
Nat Chem Biol. 2020 Dec;16(12):1321-1330
pubmed: 33199908
ACS Cent Sci. 2018 Jun 27;4(6):709-717
pubmed: 29974066
Nat Methods. 2021 Apr;18(4):382-388
pubmed: 33782607
J Chem Theory Comput. 2018 Nov 13;14(11):6050-6062
pubmed: 30253091
Nat Protoc. 2018 Sep;13(9):2086-2101
pubmed: 30190552
Biophys J. 2018 Jan 9;114(1):146-157
pubmed: 29320681
Nat Chem Biol. 2020 Jun;16(6):644-652
pubmed: 32367017
J Chem Theory Comput. 2021 Feb 9;17(2):1170-1180
pubmed: 33475352
Biophys J. 2021 Jun 15;120(12):2370-2373
pubmed: 33940023
Biophys J. 2014 Nov 18;107(10):2337-44
pubmed: 25418302
Biophys J. 2020 Sep 1;119(5):892-899
pubmed: 32814063
J Phys Chem B. 2007 Jul 12;111(27):7812-24
pubmed: 17569554

Auteurs

Martin Girard (M)

Max Planck Institute for Polymer Research, Mainz, Germany. Electronic address: martin.girard@mpip-mainz.mpg.de.

Tristan Bereau (T)

Max Planck Institute for Polymer Research, Mainz, Germany; Van 't Hoff Institute for Molecular Sciences and Informatics Institute, University of Amsterdam, Amsterdam, the Netherlands.

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