The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Raft domains of variable properties and compositions in plasma membrane vesicles
Open accessAbstract
Biological membranes are compartmentalized for functional diversity by a variety of specific protein–protein, protein–lipid, and lipid–lipid interactions. A subset of these are the preferential interactions between sterols, sphingolipids, and saturated aliphatic lipid tails responsible for liquid–liquid domain coexistence in eukaryotic membranes, which give rise to dynamic, nanoscopic assemblies whose coalescence is regulated by specific biochemical cues. Microscopic phase separation recently observed in isolated plasma membranes (giant plasma membrane vesicles and plasma membrane spheres) ( i ) confirms the capacity of compositionally complex membranes to phase separate, ( ii ) reflects the nanoscopic organization of live cell membranes, and ( iii ) provides a versatile platform for the investigation of the compositions and properties of the phases. Here, we show that the properties of coexisting phases in giant plasma membrane vesicles are dependent on isolation conditions—namely, the chemicals used to induce membrane blebbing. We observe strong correlations between the relative compositions and orders of the coexisting phases, and their resulting miscibility. Chemically unperturbed plasma membranes reflect these properties and validate the observations in chemically induced vesicles. Most importantly, we observe domains with a continuum of varying stabilities, orders, and compositions induced by relatively small differences in isolation conditions. These results show that, based on the principle of preferential association of raft lipids, domains of various properties can be produced in a membrane environment whose complexity is reflective of biological membranes.
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Cites
Tetraspanin functions and associated microdomains
Hemler, M. E. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1736 · Cited by 1,355 · cited 1×
“, in NEM GPMVs) could be the physicochemical analogs of various “nonraft” PM domains inferred from biochemical and nanoscopic observations, including GPI- anchored protein (AP) domains (24), heavy rafts (25), Lubrol rafts (26), Hras domains (27), T-cell receptor islands (28), and tetraspanin webs (29).”
BackgroundRegulation of human EGF receptor by lipids
Coskun, Ü., Grzybek, M., Drechsel, D., & Simons, K. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105666108 · Cited by 316
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Cited by
The mystery of membrane organization: composition, regulation and roles of lipid rafts
Sezgin, E., Levental, I., Mayor, S., & Eggeling, C. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.16 · Cited by 2,124
Self-citationElucidating membrane structure and protein behavior using giant plasma membrane vesicles
Sezgin, E., Kaiser, H.-J., Baumgart, T., Schwille, P., Simons, K., & Levental, I. (2012) · Nature Protocols · doi:10.1038/nprot.2012.059 · Cited by 527
Self-citationMolecular Dynamics Simulations of Membrane Permeability
Venable, R. M., Krämer, A., & Pastor, R. W. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00486 · Cited by 394
Regulation of Transmembrane Signaling by Phase Separation
Case, L. B., Ditlev, J. A., & Rosen, M. K. (2019) · Annual Review of Biophysics · doi:10.1146/annurev-biophys-052118-115534 · Cited by 303
Structural determinants and functional consequences of protein affinity for membrane rafts
Lorent, J. H., Diaz-Rohrer, B., Lin, X., Spring, K., Gorfe, A. A., Levental, K. R., & Levental, I. (2017) · Nature Communications · doi:10.1038/s41467-017-01328-3 · Cited by 283
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Metadata
- Authors
- Levental, I., Grzybek, M., & Simons, K.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2011-06-27
- Volume
- 108
- Issue
- 28
- Pages
- 11411-11416
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2160165571
- Cited by
- 246
- References
- 2
- FWCI
- 5.05
- Type
- journal article
- Language
- en
- Open access
- green
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