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      Loss of plasma membrane lipid asymmetry can induce ordered domain (raft) formation

      research-article
      , , ,
      Journal of Lipid Research
      American Society for Biochemistry and Molecular Biology
      lipid rafts, membrane domains, liquid ordered, fluorescence anisotropy, fluorescence resonance energy transfer, plasma membrane vesicles, leaflet asymmetry, N-ethyl maleimide, dithiothreitol, annexin, ABB, annexin-binding buffer, aLUV, asymmetric large unilamellar vesicles, DOPE, 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-N-(lissamine rhodamine B sulfonyl), DPH, 1,6-diphenyl-1,3,5-hexatriene, FAST DiO, 3,3′-dilinoleyloxacarbocyanine perchlorate, FRET, fluorescence resonance energy transfer, GPMV, giant plasma membrane vesicles, Ld, liquid-disordered state, Lo, liquid-ordered state, ODRB, octydecylrhodamine B, OG, octyl glucoside, PFA, paraformaldehyde, PM, plasma membrane, PMVs, plasma membrane vesicles, ProK, proteinase K, sLUV, symmetric large unilamellar vesicles

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          Abstract

          In some cases, lipids in one leaflet of an asymmetric artificial lipid vesicle suppress the formation of ordered lipid domains (rafts) in the opposing leaflet. Whether this occurs in natural membranes is unknown. Here, we investigated this issue using plasma membrane vesicles (PMVs) from rat leukemia RBL-2H3 cells. Membrane domain formation and order was assessed by fluorescence resonance energy transfer and fluorescence anisotropy. We found that ordered domains in PMVs prepared from cells by N-ethyl maleimide (NEM) treatment formed up to ∼37°C, whereas ordered domains in symmetric vesicles formed from the extracted PMV lipids were stable up to 55°C, indicating the stability of ordered domains was substantially decreased in intact PMVs. This behavior paralleled lesser ordered domain stability in artificial asymmetric lipid vesicles relative to the corresponding symmetric vesicles, suggesting intact PMVs exhibit some degree of lipid asymmetry. This was supported by phosphatidylserine mislocalization on PMV outer leaflets as judged by annexin binding, which indicated NEM-induced PMVs are much more asymmetric than PMVs formed by dithiothreitol/paraformaldehyde treatment. Destroying asymmetry by reconstitution of PMVs using detergent dilution also showed stabilization of domain formation, even though membrane proteins remained associated with reconstituted vesicles. Similar domain stabilization was observed in artificial asymmetric lipid vesicles after destroying asymmetry via detergent reconstitution. Proteinase K digestion of proteins had little effect on domain stability in NEM PMVs. We conclude that loss of PMV lipid asymmetry can induce ordered domain formation. The dynamic control of lipid asymmetry in cells may regulate domain formation in plasma membranes.

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          The mystery of membrane organization: composition, regulation and roles of lipid rafts

          Lipid rafts are relatively ordered membrane domains that are enriched in cholesterol and saturated lipids, and selectively recruit other lipids and proteins. They are dynamic and heterogeneous in composition and are thus challenging to visualize in vivo. New technologies are providing novel insights into the formation, organization and functions of these membrane domains.
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            Calcium-dependent phospholipid scrambling by TMEM16F.

            In all animal cells, phospholipids are asymmetrically distributed between the outer and inner leaflets of the plasma membrane. This asymmetrical phospholipid distribution is disrupted in various biological systems. For example, when blood platelets are activated, they expose phosphatidylserine (PtdSer) to trigger the clotting system. The PtdSer exposure is believed to be mediated by Ca(2+)-dependent phospholipid scramblases that transport phospholipids bidirectionally, but its molecular mechanism is still unknown. Here we show that TMEM16F (transmembrane protein 16F) is an essential component for the Ca(2+)-dependent exposure of PtdSer on the cell surface. When a mouse B-cell line, Ba/F3, was treated with a Ca(2+) ionophore under low-Ca(2+) conditions, it reversibly exposed PtdSer. Using this property, we established a Ba/F3 subline that strongly exposed PtdSer by repetitive fluorescence-activated cell sorting. A complementary DNA library was constructed from the subline, and a cDNA that caused Ba/F3 to expose PtdSer spontaneously was identified by expression cloning. The cDNA encoded a constitutively active mutant of TMEM16F, a protein with eight transmembrane segments. Wild-type TMEM16F was localized on the plasma membrane and conferred Ca(2+)-dependent scrambling of phospholipids. A patient with Scott syndrome, which results from a defect in phospholipid scrambling activity, was found to carry a mutation at a splice-acceptor site of the gene encoding TMEM16F, causing the premature termination of the protein.
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              Plasma membranes are asymmetric in lipid unsaturation, packing, and protein shape

              SUMMARY: A fundamental feature of cellular plasma membranes (PM) is 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 ~2-fold more unsaturated than the exoplasmic. 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 asymmetric structures of protein transmembrane domains (TMD). These structural asymmetries are conserved throughout Eukaryota, suggesting fundamental cellular design principles.
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                Author and article information

                Contributors
                Journal
                J Lipid Res
                J Lipid Res
                Journal of Lipid Research
                American Society for Biochemistry and Molecular Biology
                0022-2275
                1539-7262
                26 November 2021
                January 2022
                26 November 2021
                : 63
                : 1
                : 100155
                Affiliations
                [1]Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY, USA
                Author notes
                []For correspondence: Erwin London erwin.london@ 123456stonybrook.edu
                [‡]

                These authors contributed equally to this report.

                Article
                S0022-2275(21)00138-3 100155
                10.1016/j.jlr.2021.100155
                8953672
                34843684
                1809799a-6bee-4c0b-a7e3-f38407df152e
                © 2021 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 5 November 2021
                : 23 November 2021
                Categories
                Research Article

                Biochemistry
                lipid rafts,membrane domains,liquid ordered,fluorescence anisotropy,fluorescence resonance energy transfer,plasma membrane vesicles,leaflet asymmetry,n-ethyl maleimide,dithiothreitol,annexin,abb, annexin-binding buffer,aluv, asymmetric large unilamellar vesicles,dope, 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine-n-(lissamine rhodamine b sulfonyl),dph, 1,6-diphenyl-1,3,5-hexatriene,fast dio, 3,3′-dilinoleyloxacarbocyanine perchlorate,fret, fluorescence resonance energy transfer,gpmv, giant plasma membrane vesicles,ld, liquid-disordered state,lo, liquid-ordered state,odrb, octydecylrhodamine b,og, octyl glucoside,pfa, paraformaldehyde,pm, plasma membrane,pmvs, plasma membrane vesicles,prok, proteinase k,sluv, symmetric large unilamellar vesicles

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