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Membrane Asymmetry and Phospholipid Translocases in Eukaryotic Cells

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Abstract

Membranes provide an essential physical boundary to the cell, allowing separation of a living cell from its environment, as well as subcellular compartmentalization of functional organelles in eukaryotic cells. Each membrane has a unique lipid and protein composition, which is optimized for its function as the interface between the extracellular and intracellular environments. As the primary structural component of this interface, phospholipids form the membrane bilayer backbone, and provide the major barrier function and other functions such as signal transduction and molecular recognition. One crucial feature of membrane phospholipids is their asymmetrical distribution between the two leaflets in various cell membranes, which appears to be a common theme from yeast to human cells. For example, in the plasma membrane of red blood cells, the extracellular leaflet is predominantly occupied by phosphatidylcholine (PtdCho) and sphingomyelin (SM), while the cytosolic leaflet is enriched in phosphatidylserine (PtdSer) and phosphatidylethanolamine (PtdEtn). The asymmetric distribution of membrane lipids and their regulated transbilayer movement plays important roles in many cellular processes and functions, including apoptosis, blood coagulation and cell membrane integrity. But how is membrane lipid asymmetry generated and maintained? More specifically, how do phospholipids traverse the membrane bilayer, known as flip-flop, in a living cell? Since phospholipids are amphipathic molecules with large polar groups, their movement across the hydrophobic membrane interior is thermodynamically unfavorable. Experimental evidence demonstrates that in biological membranes, this process is mediated and facilitated by a number of membrane proteins, which function as phospholipid translocases that include P4-ATPases, ATP-binding cassette (ABC) transporters, TMEM16 family members, and others. Furthermore, recent advancement of structural studies on some of these proteins starts to shed light on the molecular mechanisms of phospholipid translocation by lipid translocases. In this chapter, we review our knowledge on phospholipid translocases in eukaryotic cells, and discuss our current understanding toward their functions and mechanisms.

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References

  1. van Meer G, Voelker DR, Feigenson GW. Membrane lipids: where they are and how they behave. Nat Rev Mol Cell Biol. 2008;9:112–24. https://doi.org/10.1038/nrm2330.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  2. Spector AA, Yorek MA. Membrane lipid composition and cellular function. J Lipid Res. 1985;26:1015–35.

    PubMed  CAS  Google Scholar 

  3. Marsh D. Lateral pressure profile, spontaneous curvature frustration, and the incorporation and conformation of proteins in membranes. Biophys J. 2007;93:3884–99. https://doi.org/10.1529/biophysj.107.107938.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  4. Sezgin E, Levental I, Mayor S, Eggeling C. The mystery of membrane organization: composition, regulation and roles of lipid rafts. Nat Rev Mol Cell Biol. 2017;18:361–74. https://doi.org/10.1038/nrm.2017.16.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  5. Bretscher MS. Membrane structure: some general principles. Science. 1973;181:622–9.

    Article  CAS  PubMed  Google Scholar 

  6. Devaux PF. Protein involvement in transmembrane lipid asymmetry. Annu Rev Biophys Biomol Struct. 1992;21:417–39. https://doi.org/10.1146/annurev.bb.21.060192.002221.

    Article  PubMed  CAS  Google Scholar 

  7. Zwaal RF, Schroit AJ. Pathophysiologic implications of membrane phospholipid asymmetry in blood cells. Blood. 1997;89:1121–32.

    PubMed  CAS  Google Scholar 

  8. Natarajan P, Wang J, Hua Z, Graham TR. Drs2p-coupled aminophospholipid translocase activity in yeast Golgi membranes and relationship to in vivo function. Proc Natl Acad Sci USA. 2004;101:10614–9. https://doi.org/10.1073/pnas.0404146101.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  9. Alder-Baerens N, Lisman Q, Luong L, Pomorski T, Holthuis JC. Loss of P4 ATPases Drs2p and Dnf3p disrupts aminophospholipid transport and asymmetry in yeast post-Golgi secretory vesicles. Mol Biol Cell. 2006;17:1632–42. https://doi.org/10.1091/mbc.E05-10-0912.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  10. Sanyal S, Menon AK. Flipping lipids: why an’ what’s the reason for? ACS Chem Biol. 2009;4:895–909. https://doi.org/10.1021/cb900163d.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  11. Fairn GD, et al. High-resolution mapping reveals topologically distinct cellular pools of phosphatidylserine. J Cell Biol. 2011;194:257–75. https://doi.org/10.1083/jcb.201012028.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  12. Higgins JA, Dawson RM. Asymmetry of the phospholipid bilayer of rat liver endoplasmic reticulum. Biochim Biophys Acta. 1977;470:342–56.

    Article  CAS  PubMed  Google Scholar 

  13. Kornberg RD, McConnell HM. Inside-outside transitions of phospholipids in vesicle membranes. Biochemistry. 1971;10:1111–20.

    Article  CAS  PubMed  Google Scholar 

  14. Anglin TC, Liu J, Conboy JC. Facile lipid flip-flop in a phospholipid bilayer induced by gramicidin A measured by sum-frequency vibrational spectroscopy. Biophys J. 2007;92:L01–3. https://doi.org/10.1529/biophysj.106.096057.

    Article  PubMed  CAS  Google Scholar 

  15. Liu J, Conboy JC. 1,2-diacyl-phosphatidylcholine flip-flop measured directly by sum-frequency vibrational spectroscopy. Biophys J. 2005;89:2522–32. https://doi.org/10.1529/biophysj.105.065672.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  16. Nakano M, et al. Flip-flop of phospholipids in vesicles: kinetic analysis with time-resolved small-angle neutron scattering. J Phys Chem B. 2009;113:6745–8. https://doi.org/10.1021/jp900913w.

    Article  PubMed  CAS  Google Scholar 

  17. Hankins HM, Baldridge RD, Xu P, Graham TR. Role of flippases, scramblases and transfer proteins in phosphatidylserine subcellular distribution. Traffic. 2015;16:35–47. https://doi.org/10.1111/tra.12233.

    Article  PubMed  CAS  Google Scholar 

  18. Daleke DL. Phospholipid flippases. J Biol Chem. 2007;282:821–5. https://doi.org/10.1074/jbc.R600035200.

    Article  PubMed  CAS  Google Scholar 

  19. Pomorski T, Holthuis JC, Herrmann A, van Meer G. Tracking down lipid flippases and their biological functions. J Cell Sci. 2004;117:805–13. https://doi.org/10.1242/jcs.01055.

    Article  PubMed  CAS  Google Scholar 

  20. Muthusamy BP, Natarajan P, Zhou X, Graham TR. Linking phospholipid flippases to vesicle-mediated protein transport. Biochim Biophys Acta. 2009;1791:612–9. https://doi.org/10.1016/j.bbalip.2009.03.004.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  21. Coleman JA, Quazi F, Molday RS. Mammalian P4-ATPases and ABC transporters and their role in phospholipid transport. Biochim Biophys Acta. 2013;1831:555–74. https://doi.org/10.1016/j.bbalip.2012.10.006.

    Article  PubMed  CAS  Google Scholar 

  22. Lopez-Marques RL, et al. Structure and mechanism of ATP-dependent phospholipid transporters. Biochim Biophys Acta. 2015;1850:461–75. https://doi.org/10.1016/j.bbagen.2014.04.008.

    Article  PubMed  CAS  Google Scholar 

  23. Andersen JP, et al. P4-ATPases as phospholipid Flippases-structure, function, and enigmas. Front Physiol. 2016;7:275. https://doi.org/10.3389/fphys.2016.00275.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Quazi F, Lenevich S, Molday RS. ABCA4 is an N-retinylidene-phosphatidylethanolamine and phosphatidylethanolamine importer. Nat Commun. 2012;3:925. https://doi.org/10.1038/ncomms1927.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  25. Williamson P. Phospholipid scramblases. Lipid Insights. 2015;8:41–4. https://doi.org/10.4137/LPI.S31785.

    Article  PubMed  Google Scholar 

  26. Bretscher MS. The cell surface in development. In: Moscona AA, editor. Wiley; 1974. pp. 17–24.

    Google Scholar 

  27. Maxfield FR, Menon AK. Biochemistry of lipids, lipoproteins and membranes. In: Ridgway ND, McLeod RS, editors. Elsevier; 2016. Ch. 14, pp. 415–36.

    Google Scholar 

  28. Seigneuret M, Devaux PF. ATP-dependent asymmetric distribution of spin-labeled phospholipids in the erythrocyte membrane: relation to shape changes. Proc Natl Acad Sci USA. 1984;81:3751–5.

    Article  CAS  PubMed  Google Scholar 

  29. Daleke DL, Huestis WH. Incorporation and translocation of aminophospholipids in human erythrocytes. Biochemistry. 1985;24:5406–16.

    Article  CAS  PubMed  Google Scholar 

  30. Daleke DL, Huestis WH. Erythrocyte morphology reflects the transbilayer distribution of incorporated phospholipids. J Cell Biol. 1989;108:1375–85.

    Article  CAS  PubMed  Google Scholar 

  31. Moriyama Y, Nelson N. Purification and properties of a vanadate- and N-ethylmaleimide-sensitive ATPase from chromaffin granule membranes. J Biol Chem. 1988;263:8521–7.

    PubMed  CAS  Google Scholar 

  32. Zachowski A, Henry JP, Devaux PF. Control of transmembrane lipid asymmetry in chromaffin granules by an ATP-dependent protein. Nature. 1989;340:75–6. https://doi.org/10.1038/340075a0.

    Article  PubMed  CAS  Google Scholar 

  33. Tang X, Halleck MS, Schlegel RA, Williamson P. A subfamily of P-type ATPases with aminophospholipid transporting activity. Science. 1996;272:1495–7.

    Article  CAS  PubMed  Google Scholar 

  34. Axelsen KB, Palmgren MG. Evolution of substrate specificities in the P-type ATPase superfamily. J Mol Evol. 1998;46:84–101.

    Article  CAS  PubMed  Google Scholar 

  35. Kuhlbrandt W. Biology, structure and mechanism of P-type ATPases. Nat Rev Mol Cell Biol. 2004;5:282–95. https://doi.org/10.1038/nrm1354.

    Article  PubMed  CAS  Google Scholar 

  36. Palmgren MG, Nissen P. P-type ATPases. Annu Rev Biophys. 2011;40:243–66. https://doi.org/10.1146/annurev.biophys.093008.131331.

    Article  PubMed  CAS  Google Scholar 

  37. Carafoli E. Biogenesis: plasma membrane calcium ATPase: 15 years of work on the purified enzyme. FASEB J. 1994;8:993–1002.

    Article  CAS  PubMed  Google Scholar 

  38. Palmgren MG. PLANT PLASMA MEMBRANE H+-ATPases: powerhouses for nutrient uptake. Annu Rev Plant Physiol Plant Mol Biol. 2001;52:817–45. https://doi.org/10.1146/annurev.arplant.52.1.817.

    Article  PubMed  CAS  Google Scholar 

  39. Portillo F. Regulation of plasma membrane H(+)-ATPase in fungi and plants. Biochim Biophys Acta. 2000;1469:31–42.

    Article  CAS  PubMed  Google Scholar 

  40. Sze H, Liang F, Hwang I, Curran AC, Harper JF. Diversity and regulation of plant Ca2+ pumps: insights from expression in yeast. Annu Rev Plant Physiol Plant Mol Biol. 2000;51:433–62. https://doi.org/10.1146/annurev.arplant.51.1.433.

    Article  PubMed  CAS  Google Scholar 

  41. Toyoshima C. How Ca2+-ATPase pumps ions across the sarcoplasmic reticulum membrane. Biochim Biophys Acta. 2009;1793:941–6. https://doi.org/10.1016/j.bbamcr.2008.10.008.

    Article  PubMed  CAS  Google Scholar 

  42. Morth JP, et al. A structural overview of the plasma membrane Na+,K+-ATPase and H+-ATPase ion pumps. Nat Rev Mol Cell Biol. 2011;12:60–70. https://doi.org/10.1038/nrm3031.

    Article  PubMed  CAS  Google Scholar 

  43. Pedersen BP, Buch-Pedersen MJ, Morth JP, Palmgren MG, Nissen P. Crystal structure of the plasma membrane proton pump. Nature. 2007;450:1111–4. https://doi.org/10.1038/nature06417.

    Article  PubMed  CAS  Google Scholar 

  44. Gourdon P, et al. Crystal structure of a copper-transporting PIB-type ATPase. Nature. 2011;475:59–64. https://doi.org/10.1038/nature10191.

    Article  PubMed  CAS  Google Scholar 

  45. Andersson M, et al. Copper-transporting P-type ATPases use a unique ion-release pathway. Nat Struct Mol Biol. 2014;21:43–8. https://doi.org/10.1038/nsmb.2721.

    Article  PubMed  CAS  Google Scholar 

  46. Wang K, et al. Structure and mechanism of Zn2+−transporting P-type ATPases. Nature. 2014;514:518–22. https://doi.org/10.1038/nature13618.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  47. Paulusma CC, Elferink RP. P4 ATPases—the physiological relevance of lipid flipping transporters. FEBS Lett. 2010;584:2708–16. https://doi.org/10.1016/j.febslet.2010.04.071.

    Article  PubMed  CAS  Google Scholar 

  48. van der Mark VA, Elferink RP, Paulusma CC. P4 ATPases: flippases in health and disease. Int J Mol Sci. 2013;14:7897–922. https://doi.org/10.3390/ijms14047897.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  49. Hua Z, Graham TR. Requirement for neo1p in retrograde transport from the Golgi complex to the endoplasmic reticulum. Mol Biol Cell. 2003;14:4971–83. https://doi.org/10.1091/mbc.E03-07-0463.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  50. Hua Z, Fatheddin P, Graham TR. An essential subfamily of Drs2p-related P-type ATPases is required for protein trafficking between Golgi complex and endosomal/vacuolar system. Mol Biol Cell. 2002;13:3162–77. https://doi.org/10.1091/mbc.E02-03-0172.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  51. Toyoshima C, Inesi G. Structural basis of ion pumping by Ca2+-ATPase of the sarcoplasmic reticulum. Annu Rev Biochem. 2004;73:269–92. https://doi.org/10.1146/annurev.biochem.73.011303.073700.

    Article  PubMed  CAS  Google Scholar 

  52. Zhou X, Natarajan P, Muthusamy BP, Graham TR, Liu K. Transmembrane dynamics of lipids. In: Devaux PF, Herrmann A, editors. Wiley; 2011, pp. 171–197.

    Chapter  Google Scholar 

  53. Vestergaard AL, et al. Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2. Proc Natl Acad Sci USA. 2014;111:E1334–43. https://doi.org/10.1073/pnas.1321165111.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  54. Baldridge RD, Graham TR. Identification of residues defining phospholipid flippase substrate specificity of type IV P-type ATPases. Proc Natl Acad Sci USA. 2012;109:E290–8. https://doi.org/10.1073/pnas.1115725109.

    Article  PubMed  PubMed Central  Google Scholar 

  55. Stone A, Williamson P. Outside of the box: recent news about phospholipid translocation by P4 ATPases. J Chem Biol. 2012;5:131–6. https://doi.org/10.1007/s12154-012-0078-x.

    Article  PubMed  PubMed Central  Google Scholar 

  56. Baldridge RD, Graham TR. Two-gate mechanism for phospholipid selection and transport by type IV P-type ATPases. Proc Natl Acad Sci USA. 2013;110:E358–67. https://doi.org/10.1073/pnas.1216948110.

    Article  PubMed  PubMed Central  Google Scholar 

  57. Zhou X, Sebastian TT, Graham TR. Auto-inhibition of Drs2p, a yeast phospholipid flippase, by its carboxyl-terminal tail. J Biol Chem. 2013;288:31807–15. https://doi.org/10.1074/jbc.M113.481986.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  58. Takatsu H, et al. ATP9B, a P4-ATPase (a putative aminophospholipid translocase), localizes to the trans-Golgi network in a CDC50 protein-independent manner. J Biol Chem. 2011;286:38159–67. https://doi.org/10.1074/jbc.M111.281006.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  59. Chalat M, Moleschi K, Molday RS. C-terminus of the P4-ATPase ATP8A2 functions in protein folding and regulation of phospholipid flippase activity. Mol Biol Cell. 2017;28:452–62. https://doi.org/10.1091/mbc.E16-06-0453.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  60. Katoh Y, Katoh M. Identification and characterization of CDC50A, CDC50B and CDC50C genes in silico. Oncol Rep. 2004;12:939–43.

    PubMed  CAS  Google Scholar 

  61. Saito K, et al. Cdc50p, a protein required for polarized growth, associates with the Drs2p P-type ATPase implicated in phospholipid translocation in Saccharomyces cerevisiae. Mol Biol Cell. 2004;15:3418–32. https://doi.org/10.1091/mbc.E03-11-0829.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  62. Bryde S, et al. CDC50 proteins are critical components of the human class-1 P4-ATPase transport machinery. J Biol Chem. 2010;285:40562–72. https://doi.org/10.1074/jbc.M110.139543.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  63. Chen S, et al. Roles for the Drs2p-Cdc50p complex in protein transport and phosphatidylserine asymmetry of the yeast plasma membrane. Traffic. 2006;7:1503–17. https://doi.org/10.1111/j.1600-0854.2006.00485.x.

    Article  PubMed  CAS  Google Scholar 

  64. Furuta N, Fujimura-Kamada K, Saito K, Yamamoto T, Tanaka K. Endocytic recycling in yeast is regulated by putative phospholipid translocases and the Ypt31p/32p-Rcy1p pathway. Mol Biol Cell. 2007;18:295–312. https://doi.org/10.1091/mbc.E06-05-0461.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  65. Lenoir G, Williamson P, Puts CF, Holthuis JC. Cdc50p plays a vital role in the ATPase reaction cycle of the putative aminophospholipid transporter Drs2p. J Biol Chem. 2009;284:17956–67. https://doi.org/10.1074/jbc.M109.013722.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  66. Vestergaard AL, et al. Specific mutations in mammalian P4-ATPase ATP8A2 catalytic subunit entail differential glycosylation of the accessory CDC50A subunit. FEBS Lett. 2015;589:3908–14. https://doi.org/10.1016/j.febslet.2015.11.031.

    Article  PubMed  CAS  Google Scholar 

  67. Geering K. The functional role of beta subunits in oligomeric P-type ATPases. J Bioenerg Biomembr. 2001;33:425–38.

    Article  CAS  PubMed  Google Scholar 

  68. Catty P, de Kerchove d’Exaerde A, Goffeau A. The complete inventory of the yeast Saccharomyces cerevisiae P-type transport ATPases. FEBS Lett. 1997;409:325–32.

    Article  CAS  PubMed  Google Scholar 

  69. Wicky S, Schwarz H, Singer-Kruger B. Molecular interactions of yeast Neo1p, an essential member of the Drs2 family of aminophospholipid translocases, and its role in membrane trafficking within the endomembrane system. Mol Cell Biol. 2004;24:7402–18. https://doi.org/10.1128/MCB.24.17.7402-7418.2004.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  70. Barbosa S, Pratte D, Schwarz H, Pipkorn R, Singer-Kruger B. Oligomeric Dop1p is part of the endosomal Neo1p-Ysl2p-Arl1p membrane remodeling complex. Traffic. 2010;11:1092–106. https://doi.org/10.1111/j.1600-0854.2010.01079.x.

    Article  PubMed  CAS  Google Scholar 

  71. Sakane H, Yamamoto T, Tanaka K. The functional relationship between the Cdc50p-Drs2p putative aminophospholipid translocase and the Arf GAP Gcs1p in vesicle formation in the retrieval pathway from yeast early endosomes to the TGN. Cell Struct Funct. 2006;31:87–108.

    Article  CAS  PubMed  Google Scholar 

  72. Xu P, Baldridge RD, Chi RJ, Burd CG, Graham TR. Phosphatidylserine flipping enhances membrane curvature and negative charge required for vesicular transport. J Cell Biol. 2013;202:875–86. https://doi.org/10.1083/jcb.201305094.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  73. van der Velden LM, et al. Heteromeric interactions required for abundance and subcellular localization of human CDC50 proteins and class 1 P4-ATPases. J Biol Chem. 2010;285:40088–96. https://doi.org/10.1074/jbc.M110.139006.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  74. Takatsu H, et al. Phospholipid flippase activities and substrate specificities of human type IV P-type ATPases localized to the plasma membrane. J Biol Chem. 2014;289:33543–56. https://doi.org/10.1074/jbc.M114.593012.

    Article  PubMed  CAS  Google Scholar 

  75. Naito T, et al. Phospholipid Flippase ATP10A translocates phosphatidylcholine and is involved in plasma membrane dynamics. J Biol Chem. 2015;290:15004–17. https://doi.org/10.1074/jbc.M115.655191.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  76. Coleman JA, Molday RS. Critical role of the beta-subunit CDC50A in the stable expression, assembly, subcellular localization, and lipid transport activity of the P4-ATPase ATP8A2. J Biol Chem. 2011;286:17205–16. https://doi.org/10.1074/jbc.M111.229419.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  77. Lee S, et al. Transport through recycling endosomes requires EHD1 recruitment by a phosphatidylserine translocase. EMBO J. 2015;34:669–88. https://doi.org/10.15252/embj.201489703.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  78. Segawa K, Kurata S, Nagata S. Human type IV P-type ATPases that work as plasma membrane phospholipid Flippases and their regulation by caspase and calcium. J Biol Chem. 2016;291:762–72. https://doi.org/10.1074/jbc.M115.690727.

    Article  PubMed  CAS  Google Scholar 

  79. Siegmund A, et al. Loss of Drs2p does not abolish transfer of fluorescence-labeled phospholipids across the plasma membrane of Saccharomyces cerevisiae. J Biol Chem. 1998;273:34399–405.

    Article  CAS  PubMed  Google Scholar 

  80. Marx U, et al. Rapid transbilayer movement of fluorescent phospholipid analogues in the plasma membrane of endocytosis-deficient yeast cells does not require the Drs2 protein. Eur J Biochem. 1999;263:254–63.

    Article  CAS  PubMed  Google Scholar 

  81. Gomes E, Jakobsen MK, Axelsen KB, Geisler M, Palmgren MG. Chilling tolerance in Arabidopsis involves ALA1, a member of a new family of putative aminophospholipid translocases. Plant Cell. 2000;12:2441–54.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Zhou X, Graham TR. Reconstitution of phospholipid translocase activity with purified Drs2p, a type-IV P-type ATPase from budding yeast. Proc Natl Acad Sci USA. 2009;106:16586–91. https://doi.org/10.1073/pnas.0904293106.

    Article  PubMed  PubMed Central  Google Scholar 

  83. Baldridge RD, Xu P, Graham TR. Type IV P-type ATPases distinguish mono- versus diacyl phosphatidylserine using a cytofacial exit gate in the membrane domain. J Biol Chem. 2013;288:19516–27. https://doi.org/10.1074/jbc.M113.476911.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  84. Pomorski T, et al. Drs2p-related P-type ATPases Dnf1p and Dnf2p are required for phospholipid translocation across the yeast plasma membrane and serve a role in endocytosis. Mol Biol Cell. 2003;14:1240–54. https://doi.org/10.1091/mbc.E02-08-0501.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  85. Coleman JA, Kwok MC, Molday RS. Localization, purification, and functional reconstitution of the P4-ATPase Atp8a2, a phosphatidylserine flippase in photoreceptor disc membranes. J Biol Chem. 2009;284:32670–9. https://doi.org/10.1074/jbc.M109.047415.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  86. Ding J, et al. Identification and functional expression of four isoforms of ATPase II, the putative aminophospholipid translocase. Effect of isoform variation on the ATPase activity and phospholipid specificity. J Biol Chem. 2000;275:23378–86. https://doi.org/10.1074/jbc.M910319199.

    Article  PubMed  CAS  Google Scholar 

  87. Paterson JK, et al. Lipid specific activation of the murine P4-ATPase Atp8a1 (ATPase II). Biochemistry. 2006;45:5367–76. https://doi.org/10.1021/bi052359b.

    Article  PubMed  CAS  Google Scholar 

  88. Soupene E, Kemaladewi DU, Kuypers FA. ATP8A1 activity and phosphatidylserine transbilayer movement. J Receptor Ligand Channel Res. 2008;1:1–10.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  89. Coleman JA, Vestergaard AL, Molday RS, Vilsen B, Andersen JP. Critical role of a transmembrane lysine in aminophospholipid transport by mammalian photoreceptor P4-ATPase ATP8A2. Proc Natl Acad Sci USA. 2012;109:1449–54. https://doi.org/10.1073/pnas.1108862109.

    Article  PubMed  PubMed Central  Google Scholar 

  90. Bull LN, et al. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nat Genet. 1998;18:219–24. https://doi.org/10.1038/ng0398-219.

    Article  PubMed  CAS  Google Scholar 

  91. Folmer DE, Elferink RP, Paulusma CC. P4 ATPases—lipid flippases and their role in disease. Biochim Biophys Acta. 2009;1791:628–35. https://doi.org/10.1016/j.bbalip.2009.02.008.

    Article  PubMed  CAS  Google Scholar 

  92. Paulusma CC, et al. Atp8b1 deficiency in mice reduces resistance of the canalicular membrane to hydrophobic bile salts and impairs bile salt transport. Hepatology. 2006;44:195–204. https://doi.org/10.1002/hep.21212.

    Article  PubMed  CAS  Google Scholar 

  93. Paulusma CC, et al. ATP8B1 requires an accessory protein for endoplasmic reticulum exit and plasma membrane lipid flippase activity. Hepatology. 2008;47:268–78. https://doi.org/10.1002/hep.21950.

    Article  PubMed  CAS  Google Scholar 

  94. Ray NB, et al. Dynamic regulation of cardiolipin by the lipid pump Atp8b1 determines the severity of lung injury in experimental pneumonia. Nat Med. 2010;16:1120–7. https://doi.org/10.1038/nm.2213.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  95. Natarajan P, et al. Regulation of a Golgi flippase by phosphoinositides and an ArfGEF. Nat Cell Biol. 2009;11:1421–6. https://doi.org/10.1038/ncb1989.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  96. Muthusamy BP, et al. Control of protein and sterol trafficking by antagonistic activities of a type IV P-type ATPase and oxysterol binding protein homologue. Mol Biol Cell. 2009;20:2920–31. https://doi.org/10.1091/mbc.E08-10-1036.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  97. Hankins HM, Sere YY, Diab NS, Menon AK, Graham TR. Phosphatidylserine translocation at the yeast trans-Golgi network regulates protein sorting into exocytic vesicles. Mol Biol Cell. 2015;26:4674–85. https://doi.org/10.1091/mbc.E15-07-0487.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  98. Tsai PC, Hsu JW, Liu YW, Chen KY, Lee FJ. Arl1p regulates spatial membrane organization at the trans-Golgi network through interaction with Arf-GEF Gea2p and flippase Drs2p. Proc Natl Acad Sci USA. 2013;110:E668–77. https://doi.org/10.1073/pnas.1221484110.

    Article  PubMed  PubMed Central  Google Scholar 

  99. Hanamatsu H, Fujimura-Kamada K, Yamamoto T, Furuta N, Tanaka K. Interaction of the phospholipid flippase Drs2p with the F-box protein Rcy1p plays an important role in early endosome to trans-Golgi network vesicle transport in yeast. J Biochem. 2014;155:51–62. https://doi.org/10.1093/jb/mvt094.

    Article  PubMed  CAS  Google Scholar 

  100. Nakano K, Yamamoto T, Kishimoto T, Noji T, Tanaka K. Protein kinases Fpk1p and Fpk2p are novel regulators of phospholipid asymmetry. Mol Biol Cell. 2008;19:1783–97. https://doi.org/10.1091/mbc.E07-07-0646.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  101. Roelants FM, Baltz AG, Trott AE, Fereres S, Thorner J. A protein kinase network regulates the function of aminophospholipid flippases. Proc Natl Acad Sci USA. 2010;107:34–9. https://doi.org/10.1073/pnas.0912497106.

    Article  PubMed  Google Scholar 

  102. Roelants FM, et al. Protein kinase Gin4 negatively regulates flippase function and controls plasma membrane asymmetry. J Cell Biol. 2015;208:299–311. https://doi.org/10.1083/jcb.201410076.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  103. Jardetzky O. Simple allosteric model for membrane pumps. Nature. 1966;211:969–70.

    Article  CAS  PubMed  Google Scholar 

  104. Onat OE, et al. Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. Eur J Hum Genet. 2013;21:281–5. https://doi.org/10.1038/ejhg.2012.170.

    Article  PubMed  CAS  Google Scholar 

  105. Jacquot A, et al. Phosphatidylserine stimulation of Drs2p.Cdc50p lipid translocase dephosphorylation is controlled by phosphatidylinositol-4-phosphate. J Biol Chem. 2012;287:13249–61. https://doi.org/10.1074/jbc.M111.313916.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  106. Post RL, Hegyvary C, Kume S. Activation by adenosine triphosphate in the phosphorylation kinetics of sodium and potassium ion transport adenosine triphosphatase. J Biol Chem. 1972;247:6530–40.

    PubMed  CAS  Google Scholar 

  107. Rees DC, Johnson E, Lewinson O. ABC transporters: the power to change. Nat Rev Mol Cell Biol. 2009;10:218–27. https://doi.org/10.1038/nrm2646.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  108. Hvorup RN, et al. Asymmetry in the structure of the ABC transporter-binding protein complex BtuCD-BtuF. Science. 2007;317:1387–90. https://doi.org/10.1126/science.1145950.

    Article  PubMed  CAS  Google Scholar 

  109. Ward A, Reyes CL, Yu J, Roth CB, Chang G. Flexibility in the ABC transporter MsbA: alternating access with a twist. Proc Natl Acad Sci USA. 2007;104:19005–10. https://doi.org/10.1073/pnas.0709388104.

    Article  PubMed  PubMed Central  Google Scholar 

  110. Gadsby DC, Vergani P, Csanady L. The ABC protein turned chloride channel whose failure causes cystic fibrosis. Nature. 2006;440:477–83. https://doi.org/10.1038/nature04712.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  111. Kemp S, et al. ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations. Hum Mutat. 2001;18:499–515. https://doi.org/10.1002/humu.1227.

    Article  PubMed  CAS  Google Scholar 

  112. Oram JF. Tangier disease and ABCA1. Biochim Biophys Acta. 2000;1529:321–30.

    Article  CAS  PubMed  Google Scholar 

  113. Allikmets R, et al. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy. Nat Genet. 1997;15:236–46. https://doi.org/10.1038/ng0397-236.

    Article  PubMed  CAS  Google Scholar 

  114. Strautnieks SS, et al. A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis. Nat Genet. 1998;20:233–8. https://doi.org/10.1038/3034.

    Article  PubMed  CAS  Google Scholar 

  115. Paulusma CC, et al. A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome. Hepatology. 1997;25:1539–42. https://doi.org/10.1002/hep.510250635.

    Article  PubMed  CAS  Google Scholar 

  116. Allikmets R, et al. Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A). Hum Mol Genet. 1999;8:743–9.

    Article  CAS  PubMed  Google Scholar 

  117. Nessa A, Rahman SA, Hussain K. Hyperinsulinemic hypoglycemia—the molecular mechanisms. Front Endocrinol (Lausanne). 2016;7:29. https://doi.org/10.3389/fendo.2016.00029.

    Article  Google Scholar 

  118. Choi CH. ABC transporters as multidrug resistance mechanisms and the development of chemosensitizers for their reversal. Cancer Cell Int. 2005;5:30. https://doi.org/10.1186/1475-2867-5-30.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  119. Vasiliou V, Vasiliou K, Nebert DW. Human ATP-binding cassette (ABC) transporter family. Hum Genomics. 2009;3:281–90.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  120. Dean M, Hamon Y, Chimini G. The human ATP-binding cassette (ABC) transporter superfamily. J Lipid Res. 2001;42:1007–17.

    PubMed  CAS  Google Scholar 

  121. Raviv Y, Pollard HB, Bruggemann EP, Pastan I, Gottesman MM. Photosensitized labeling of a functional multidrug transporter in living drug-resistant tumor cells. J Biol Chem. 1990;265:3975–80.

    PubMed  CAS  Google Scholar 

  122. Locher KP. Structure and mechanism of ABC transporters. Curr Opin Struct Biol. 2004;14:426–31. https://doi.org/10.1016/j.sbi.2004.06.005.

    Article  PubMed  CAS  Google Scholar 

  123. Aller SG, et al. Structure of P-glycoprotein reveals a molecular basis for poly-specific drug binding. Science. 2009;323:1718–22. https://doi.org/10.1126/science.1168750.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  124. Johnson ZL, Chen J. Structural Basis of Substrate Recognition by the Multidrug Resistance Protein MRP1. Cell. 2017;168:1075–85 e1079. https://doi.org/10.1016/j.cell.2017.01.041.

    Article  PubMed  CAS  Google Scholar 

  125. Backer JM, Dawidowicz EA. Reconstitution of a phospholipid flippase from rat liver microsomes. Nature. 1987;327:341–3. https://doi.org/10.1038/327341a0.

    Article  PubMed  Google Scholar 

  126. Herrmann A, Zachowski A, Devaux PF. Protein-mediated phospholipid translocation in the endoplasmic reticulum with a low lipid specificity. Biochemistry. 1990;29:2023–7.

    Article  CAS  PubMed  Google Scholar 

  127. Kubelt J, Menon AK, Muller P, Herrmann A. Transbilayer movement of fluorescent phospholipid analogues in the cytoplasmic membrane of Escherichia coli. Biochemistry. 2002;41:5605–12.

    Article  CAS  PubMed  Google Scholar 

  128. Menon I, et al. Opsin is a phospholipid flippase. Curr Biol. 2011;21:149–53. https://doi.org/10.1016/j.cub.2010.12.031.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  129. Goren MA, et al. Constitutive phospholipid scramblase activity of a G protein-coupled receptor. Nat Commun. 2014;5:5115. https://doi.org/10.1038/ncomms6115.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  130. Basse F, Stout JG, Sims PJ, Wiedmer T. Isolation of an erythrocyte membrane protein that mediates Ca2+-dependent transbilayer movement of phospholipid. J Biol Chem. 1996;271:17205–10.

    Article  CAS  PubMed  Google Scholar 

  131. Zhou Q, Zhao J, Wiedmer T, Sims PJ. Normal hemostasis but defective hematopoietic response to growth factors in mice deficient in phospholipid scramblase 1. Blood. 2002;99:4030–8. https://doi.org/10.1182/blood-2001-12-0271.

    Article  PubMed  CAS  Google Scholar 

  132. Ben-Efraim I, Zhou Q, Wiedmer T, Gerace L, Sims PJ. Phospholipid scramblase 1 is imported into the nucleus by a receptor-mediated pathway and interacts with DNA. Biochemistry. 2004;43:3518–26. https://doi.org/10.1021/bi0356911.

    Article  PubMed  CAS  Google Scholar 

  133. Castoldi E, Collins PW, Williamson PL, Bevers EM. Compound heterozygosity for 2 novel TMEM16F mutations in a patient with Scott syndrome. Blood. 2011;117:4399–400. https://doi.org/10.1182/blood-2011-01-332502.

    Article  PubMed  CAS  Google Scholar 

  134. Suzuki J, Umeda M, Sims PJ, Nagata S. Calcium-dependent phospholipid scrambling by TMEM16F. Nature. 2010;468:834–8. https://doi.org/10.1038/nature09583.

    Article  PubMed  CAS  Google Scholar 

  135. Pedemonte N, Galietta LJ. Structure and function of TMEM16 proteins (anoctamins). Physiol Rev. 2014;94:419–59. https://doi.org/10.1152/physrev.00039.2011.

    Article  PubMed  CAS  Google Scholar 

  136. Malvezzi M, et al. Ca2+−dependent phospholipid scrambling by a reconstituted TMEM16 ion channel. Nat Commun. 2013;4:2367. https://doi.org/10.1038/ncomms3367.

    Article  PubMed  PubMed Central  Google Scholar 

  137. Brunner JD, Lim NK, Schenck S, Duerst A, Dutzler R. X-ray structure of a calcium-activated TMEM16 lipid scramblase. Nature. 2014;516:207–12. https://doi.org/10.1038/nature13984.

    Article  PubMed  CAS  Google Scholar 

  138. Lee BC, Menon AK, Accardi A. The nhTMEM16 scramblase is also a nonselective Ion Channel. Biophys J. 2016;111:1919–24. https://doi.org/10.1016/j.bpj.2016.09.032.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  139. Williamson P, Schlegel RA. Transbilayer phospholipid movement and the clearance of apoptotic cells. Biochim Biophys Acta. 2002;1585:53–63.

    Article  CAS  PubMed  Google Scholar 

  140. Suzuki J, Denning DP, Imanishi E, Horvitz HR, Nagata S. Xk-related protein 8 and CED-8 promote phosphatidylserine exposure in apoptotic cells. Science. 2013;341:403–6. https://doi.org/10.1126/science.1236758.

    Article  PubMed  CAS  Google Scholar 

  141. Chen YZ, Mapes J, Lee ES, Skeen-Gaar RR, Xue D. Caspase-mediated activation of Caenorhabditis elegans CED-8 promotes apoptosis and phosphatidylserine externalization. Nat Commun. 2013;4:2726. https://doi.org/10.1038/ncomms3726.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  142. Paulino C, et al. Structural basis for anion conduction in the calcium-activated chloride channel TMEM16A. Elife. 2017;6. https://doi.org/10.7554/eLife.26232.

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Fan, J., Wang, X., Sun, Z., Zhou, X. (2018). Membrane Asymmetry and Phospholipid Translocases in Eukaryotic Cells. In: Cao, Y. (eds) Advances in Membrane Proteins. Springer, Singapore. https://doi.org/10.1007/978-981-13-0532-0_3

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