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Plasma membranes are asymmetric in lipid unsaturation, packing, and protein shape
- Source :
- Nature chemical biology, Nature Chemical Biology, 16(6), 644. Nature Publishing Group
- Publication Year :
- 2020
-
Abstract
- A fundamental feature of cellular plasma membranes (PMs) is an asymmetric lipid distribution between the bilayer leaflets. However, neither the detailed, comprehensive compositions of individual PM leaflets nor how these contribute to structural membrane asymmetries have been defined. We report the distinct lipidomes and biophysical properties of both monolayers in living mammalian PMs. Phospholipid unsaturation is dramatically asymmetric, with the cytoplasmic leaflet being approximately twofold more unsaturated than the exoplasmic leaflet. Atomistic simulations and spectroscopy of leaflet-selective fluorescent probes reveal that the outer PM leaflet is more packed and less diffusive than the inner leaflet, with this biophysical asymmetry maintained in the endocytic system. The structural asymmetry of the PM is reflected in the asymmetric structures of protein transmembrane domains. These structural asymmetries are conserved throughout Eukaryota, suggesting fundamental cellular design principles.
- Subjects :
- Erythrocytes
Membrane Fluidity
Protein Conformation
Lipid Bilayers
Endocytic cycle
Phospholipid
Pyridinium Compounds
Phase Transition
Article
Diffusion
03 medical and health sciences
chemistry.chemical_compound
Membrane Microdomains
Protein structure
Membrane fluidity
Humans
cardiovascular diseases
Molecular Biology
Phospholipids
Fluorescent Dyes
030304 developmental biology
0303 health sciences
Degree of unsaturation
Bilayer
Cell Membrane
Optical Imaging
030302 biochemistry & molecular biology
technology, industry, and agriculture
Membrane Proteins
Cell Biology
Lipid Metabolism
Transmembrane domain
Membrane
chemistry
Biophysics
cardiovascular system
lipids (amino acids, peptides, and proteins)
Subjects
Details
- Language :
- English
- ISSN :
- 15524469 and 15524450
- Volume :
- 16
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Nature chemical biology
- Accession number :
- edsair.doi.dedup.....3e6265baf47a572aad4d42e7d9ced549