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In Vitro Measurement of Sphingolipid Intermembrane Transport Illustrated by GLTP Superfamily Members

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Intracellular Lipid Transport

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1949))

Abstract

Herein, we describe methodological approaches for measuring in vitro transfer of sphingolipids (SLs) between membranes. The approaches rely on direct tracking of the lipid. Typically, direct tracking involves lipid labeling via attachment of fluorophores or introduction of radioactivity. Members of the GlycoLipid Transfer Protein (GLTP) superfamily are used to illustrate two broadly applicable methods for direct lipid tracking. One method relies on Förster resonance energy transfer (FRET) that enables continuous assessment of fluorophore-labeled SL transfer in real time between lipid donor and acceptor vesicles. The second method relies on tracking of radiolabeled SL transfer by separation of lipid donor and acceptor vesicles at discrete time points. The assays are readily adjustable for assessing lipid transfer (1) between various model membrane assemblies (vesicles, micelles, bicelles, nanodiscs), (2) involving other lipid types by other lipid transfer proteins, (3) with protein preparations that are either crudely or highly purified, and (4) that is spontaneous and occurs in the absence of protein.

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References

  1. Holthuis JCM, Menon AK (2014) Lipid landscapes and pipelines in membrane homeostasis. Nature 510:48–57

    Article  CAS  PubMed  Google Scholar 

  2. Drin G (2014) Topological regulation of lipid balance in cells. Annu Rev Biochem 83:51–77

    Article  CAS  PubMed  Google Scholar 

  3. Apodaca G, Brown WJ (2014) Membrane traffic research: challenges for the next decade. Front Cell Dev Biol 2:e52

    Article  Google Scholar 

  4. Tatsuta T, Scharwey M, Langer T (2014) Mitochondrial lipid trafficking. Trends Cell Biol 24:44–52

    Article  CAS  PubMed  Google Scholar 

  5. Hurlock AK, Roston RL, Wang K et al (2014) Lipid trafficking in plant cells. Traffic 15:915–932

    Article  CAS  PubMed  Google Scholar 

  6. Malinina L, Simanshu DK, Zhai X et al (2015) Sphingolipid transfer proteins defined by the GLTP-fold. Q Rev Biophys 48:281–322

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Yamaji T, Hanada K (2015) Sphingolipid metabolism and interorganellar transport: localization of sphingolipid enzymes and lipid transfer proteins. Traffic 16:101–122

    Article  CAS  PubMed  Google Scholar 

  8. Moser von Filseck J, Čopič A, Delfosse V et al (2015) Phosphatidylserine transport by ORP/Osh proteins is driven by phosphatidylinositol 4-phosphate. Science 349:432–436

    Article  CAS  PubMed  Google Scholar 

  9. Hotamisligil GS, Bernlohr DA (2015) Metabolic functions of FABPs—mechanisms and therapeutic implications. Nat Rev Endocrinol 11:592–605

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Grabon A, Khan D, Bankaitis VA (2015) Phosphatidylinositol transfer proteins and instructive regulation of lipid kinase biology. Biochim Biophys Acta 1851:724–735

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Wakana Y, Kotake R, Oyama N et al (2015) CARTS biogenesis requires VAP–lipid transfer protein complexes functioning at the endoplasmic reticulum–Golgi interface. Mol Biol Cell 26:4686–4699

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Mattjus P (2016) Specificity of the mammalian glycolipid transfer proteins. Chem Phys Lipids 194:72–78

    Article  CAS  PubMed  Google Scholar 

  13. Gallo A, Vannier C, Galli T (2016) Endoplasmic reticulum–plasma membrane associations: structures and functions. Annu Rev Cell Dev Biol 32:279–301

    Article  CAS  PubMed  Google Scholar 

  14. Tong J, Manik MK, Yang H et al (2016) Structural insights into nonvesicular lipid transport by the oxysterol binding protein homologue family. Biochim Biophys Acta 1861:928–939

    Article  CAS  PubMed  Google Scholar 

  15. Kentala H, Weber-Boyvat M, Olkkonen VM (2016) OSBP-related protein family: mediators of lipid transport and signaling at membrane contact sites. Int Rev Cell Mol Biol 321:299–340

    Article  PubMed  Google Scholar 

  16. Huang J, Ghosh R, Bankaitis VA (2016) Sec14-like phosphatidylinositol transfer proteins and the biological landscape of phosphoinositide signaling in plants. Biochim Biophys Acta 1861:1352–1364

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Salminen TA, Blomqvist K, Edqvist J (2016) Lipid transfer proteins: classification, nomenclature, structure, and function. Planta 244:971–997

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Wong LH, Levine TP (2016) Lipid transfer proteins do their thing anchored at membrane contact sites … but what is their thing? Biochem Soc Trans 44:517–527

    Article  CAS  PubMed  Google Scholar 

  19. de Campos MKF, Schaaf G (2017) The regulation of cell polarity by lipid transfer proteins of the SEC14 family. Curr Opin Plant Biol 40:158–168

    Article  CAS  Google Scholar 

  20. Wong LH, Čopič A, Levine TP (2017) Advances on the transfer of lipids by lipid transfer proteins. Trends Biochem Sci 42:516–530

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Malinina L, Patel DJ, Brown RE (2017) How α-helical motifs form functionally diverse lipid-binding compartments. Annu Rev Biochem 86:609–636

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Huang J, Mousley CJ, Dacquay L et al (2018) A lipid transfer protein signaling axis exerts dual control of cell-cycle and membrane trafficking systems. Dev Cell 44:378–391

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Mishra SK, Gao Y-G, Deng Y et al (2018) CPTP: A sphingolipid transfer protein that regulates autophagy and inflammasome activation. Autophagy 14(5):862–879

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Malinina L, Malakhova ML, Teplov A et al (2004) Structural basis for glycosphingolipid transfer specificity. Nature 430:1048–1053

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Kenoth R, Simanshu DK, Kamlekar RK et al (2010) Structural determination and tryptophan fluorescence of heterokaryon incompatibility C2 protein (HET-C2), a fungal glycolipid transfer protein (GLTP), provide novel insights into glycolipid specificity and membrane interaction by the GLTP-fold. J Biol Chem 285:13066–13078

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Simanshu DK, Kamlekar RK, Wijesinghe DS et al (2013) Nonvesicular trafficking of a ceramide-1-phosphate that regulates eicosanoids. Nature 500:463–468

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Simanshu DK, Zhai X, Munch D et al (2014) Arabidopsis accelerated cell death 11, ACD11, is a ceramide-1-phosphate transfer protein and intermediary regulator of phytoceramide levels. Cell Rep 6:388–399

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Ochoa-Lizarralde B, Gao Y-G, Popov AN et al (2018) How FAPP2 selects simple glycosphingolipids using the GLTP-fold: Structural insights into specificity. J Biol Chem (in press)

    Google Scholar 

  29. D'Angelo G, Polishchuk E, Di Tullio G et al (2007) Glycosphingolipid synthesis requires FAPP2 transfer of glucosylceramide. Nature 449:62–67

    Article  CAS  PubMed  Google Scholar 

  30. Kamlekar RK, Simanshu DK, Gao YG et al (2013) The glycolipid transfer protein (GLTP) domain of phosphoinositol 4-phosphate adaptor protein-2 (FAPP2): structure drives preference for simple neutral glycosphingolipids. Biochim Biophys Acta 1831:417–427

    Article  CAS  PubMed  Google Scholar 

  31. Bergelson LD, Molotkovsky JG, Manevich YM (1985) Lipid specific fluorescent probes in studies of biological membranes. Chem Phys Lipids 37:165–195

    Article  CAS  PubMed  Google Scholar 

  32. Molotkovsky JG, Mikhalyov II, Imbs AB et al (1991) Synthesis and characterization of new fluorescent glycolipid probes: molecular organization of glycosphingolipids in mixed composition lipid bilayer. Chem Phys Lipids 58:199–212

    Article  Google Scholar 

  33. Boldyrev IA, Zhai X, Momsen MM et al (2007) New BODIPY lipid probes for fluorescence studies of membranes. J Lipid Res 48:1518–1532

    Article  CAS  PubMed  Google Scholar 

  34. Boldyrev IA, Brown RE, Molotkovsky JG (2013) An expedient synthesis of fluorescent labeled ceramide-1-phosphate analogues. Russ J Bioorgan Chem 39:539–542

    Article  CAS  Google Scholar 

  35. Radin NS, Evangelatos GP (1981) The use of galactose oxidase in lipid labeling. J Lipid Res 22:536–541

    CAS  PubMed  Google Scholar 

  36. Brown RE, Sugar IP, Thompson TE (1985) Spontaneous transfer of gangliotetraosylceramide between phospholipid vesicles. Biochemistry 24:4082–4091

    Article  CAS  PubMed  Google Scholar 

  37. Brown RE, Thompson TE (1987) Spontaneous transfer of ganglioside GM1 between phospholipid vesicles. Biochemistry 26:5454–5460

    Article  CAS  PubMed  Google Scholar 

  38. Sonnino S, Nicolini M, Chigorno V (1996) Preparation of radiolabeled gangliosides. Glycobiology 6:479–487

    Article  CAS  PubMed  Google Scholar 

  39. Sonnino S, Chigorno V, Tettamanti G (2000) Preparation of radioactive gangliosides, 3H or 14C isotopically labeled at oligosaccharide or ceramide moieties. Methods Enzymol 311:639–656

    Article  CAS  PubMed  Google Scholar 

  40. Schwarzmann G, Sandhoff K (1987) Lysogangliosides: synthesis and use in preparing labeled gangliosides. Methods Enzymol 138:319–341

    Article  CAS  PubMed  Google Scholar 

  41. Ito M, Mitsutake S, Tani M et al (2000) Enzymatic synthesis of [14C]ceramide, [14C]glycosphingolipids, and ω-aminoceramide. Methods Enzymol 311:682–689

    Article  CAS  PubMed  Google Scholar 

  42. Li X-M, Malakhova ML, Lin X et al (2004) Human glycolipid transfer protein: Probing conformation using fluorescence spectroscopy. Biochemistry 43:10285–10294

    Article  CAS  PubMed  Google Scholar 

  43. Malakhova ML, Malinina L, Pike HM et al (2005) Point mutational analysis of the liganding site in human glycolipid transfer protein: functionality of the complex. J Biol Chem 280:26312–26320

    Article  CAS  PubMed  Google Scholar 

  44. Szoka F, Demetrios Papahadjopoulos D (1980) Comparative properties and methods of preparation of lipid vesicles (liposomes). Annu Rev Biophys Bioeng 9:467–508

    Article  CAS  PubMed  Google Scholar 

  45. Patil YP, Jadhav S (2013) Novel methods for liposome preparation. Chem Phys Lipids 177:8–18

    Article  PubMed  CAS  Google Scholar 

  46. Akbarzadeh A, Rezaei-Sadabady R, Davaran S et al (2014) Liposome: classification, preparation, and applications. Nanoscale Res Lett 8:e102

    Article  CAS  Google Scholar 

  47. Nichols JW, Pagano RE (1981) Kinetics of soluble lipid monomer diffusion between vesicles. Biochemistry 20:2783–2789

    Article  CAS  PubMed  Google Scholar 

  48. Nichols JW (1988) Kinetics of fluorescent-labeled phosphatidylcholine transfer between nonspecific lipid transfer protein and phospholipid vesicles. Biochemistry 27:1889–1896

    Article  CAS  PubMed  Google Scholar 

  49. Roseman M, Thompson TE (1980) Mechanism of the spontaneous transfer of phospholipids between bilayers. Biochemistry 19:439–444

    Article  CAS  PubMed  Google Scholar 

  50. Correa-Freire MC, Barenholz Y, Thompson TE (1982) Glucocerebroside transfer between phosphatidylcholine bilayers. Biochemistry 21:1244–1248

    Article  CAS  PubMed  Google Scholar 

  51. Abe A, Sakagami T, Yamada K et al (1985) A fluorimetric determination of the activity of glycolipid transfer protein and some properties of the protein purified from pig brain. Biochim Biophys Acta 778:239–244

    Article  Google Scholar 

  52. Wong M, Brown RE, Barenholz Y et al (1984) Glycolipid transfer protein from bovine brain. Biochemistry 23:6498–6505

    Article  CAS  PubMed  Google Scholar 

  53. Bai J, Pagano RE (1997) Measurement of spontaneous transfer and transbilayer movement of BODIPY-labeled lipids in lipid vesicles. Biochemistry 36:8840–8848

    Article  CAS  PubMed  Google Scholar 

  54. Elvington SM, Nichols JW (2007) Spontaneous, intervesicular transfer rates of fluorescent, acyl chain-labeled phosphatidylcholine analogs. Biochim Biophys Acta 1768:502–508

    Article  CAS  PubMed  Google Scholar 

  55. Mattjus P, Molotkovsky JG, Smaby JM et al (1999) A fluorescence resonance energy transfer approach for monitoring protein-mediated glycolipid transfer between vesicle membranes. Anal Biochem 268:297–304

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Mattjus P, Pike HM, Molotkovsky JG et al (2000) Charged membrane surfaces impede the protein mediated transfer of glycosphingolipids between phospholipid bilayers. Biochemistry 39:1067–1075

    Article  CAS  PubMed  Google Scholar 

  57. Mattjus P, Kline A, Pike HM et al (2002) Probing for preferential interactions among sphingolipids in bilayer vesicles using the glycolipid transfer protein. Biochemistry 41:266–273

    Article  CAS  PubMed  Google Scholar 

  58. West G, Viitanen L, Alm C et al (2008) Identification of a glycosphingolipid transfer protein GLTP1 in Arabidopsis thaliana. FEBS J 275:3421–3437

    Article  CAS  PubMed  Google Scholar 

  59. Nylund M, Mattjus P (2005) Protein mediated glycolipid transfer is inhibited FROM sphingomyelin membranes but enhanced TO sphingomyelin containing raft like membranes. Biochim Biophys Acta 1669:87–94

    Article  CAS  PubMed  Google Scholar 

  60. Nylund M, Kjellberg MA, Molotkovsky JG et al (2006) Molecular features of phospholipids that affect glycolipid transfer protein-mediated galactosylceramide transfer between vesicles. Biochim Biophys Acta 1758:807–812

    Article  CAS  PubMed  Google Scholar 

  61. Nichols JW, Pagano RE (1983) Resonance energy transfer assay of protein-mediated lipid transfer between vesicles. J Biol Chem 258:5368–5371

    CAS  PubMed  Google Scholar 

  62. Schwarzmann G, Wendeler M, Sandhoff K (2005) Synthesis of novel NBD-GM1 and NBD-GM2 for the transfer activity of GM2-activator protein by a FRET-based assay system. Glycobiology 15:1302–1311

    Article  CAS  PubMed  Google Scholar 

  63. Epand RF, Schlattner U, Wallimann T et al (2007) Novel lipid transfer property of two mitochondrial proteins that bridge the inner and outer membranes. Biophys J 92:126–137

    Article  CAS  PubMed  Google Scholar 

  64. Brown RE (1990) Spontaneous transfer of lipids between membranes. Subcell Biochem 16:333–363

    Article  CAS  PubMed  Google Scholar 

  65. Jones JD, Almeida PFF, Thompson TE (1990) Spontaneous interbilayer transfer of hexosylceramides between phospholipid bilayers. Biochemistry 29:3892–3897

    Article  CAS  PubMed  Google Scholar 

  66. Brown RE (1992) Spontaneous lipid transfer between organized lipid assemblies. Biochim Biophys Acta 1113:375–389

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  67. Brown RE, Mattjus P (2007) Glycolipid transfer proteins. Biochim Biophys Acta 1771:746–760

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Rao CS, Lin X, Pike HM et al (2004) Glycolipid transfer protein mediated transfer of glycosphingolipids between membranes: a model for action based on kinetics and thermodynamic analyses. Biochemistry 43:13805–13815

    Article  CAS  PubMed  Google Scholar 

  69. Samygina VR, Popov AN, Cabo-Bilbao A et al (2011) Structure 19:1644–1654

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  70. Brown RE, Stephenson FA, Markello T et al (1985) Properties of a specific glycolipid transfer protein from bovine brain. Chem Phys Lipids 38:79–93

    Article  CAS  PubMed  Google Scholar 

  71. Brown RE, Jarvis KL, Hyland KJ (1990) Purification and characterization of glycolipid transfer protein from bovine brain. Biochim Biophys Acta 1044:77–83

    Article  CAS  PubMed  Google Scholar 

  72. Zhai X, Gao Y-G, Mishra SK et al (2017) Phosphatidylserine stimulates ceramide 1-phosphate (C1P) intermembrane transfer by C1P transfer proteins. J Biol Chem 292:2531–2541

    Article  CAS  PubMed  Google Scholar 

  73. Brown RE, Hyland KJ (1992) Spontaneous transfer of ganglioside GM1 from its micelles to lipid vesicles of differing size. Biochemistry 31:10602–10609

    Article  CAS  PubMed  Google Scholar 

  74. Lev S (2010) Non-vesicular lipid transport by lipid-transfer proteins and beyond. Nat Rev Mol Cell Biol 11:739–750

    Article  CAS  PubMed  Google Scholar 

  75. Somerharju P (2015) Is spontaneous translocation of polar lipids between cellular organelles negligible? Lipid Insights 8(S1):87–93

    PubMed  Google Scholar 

  76. Richens JL, Tyler AII, Barriga HMG et al (2017) Spontaneous charged lipid transfer between lipid vesicles. Sci Report 7:e12606

    Article  CAS  Google Scholar 

  77. Shenkarev ZO, Melnikova DN, Finkina EI et al (2017) Ligand binding properties of the lentil lipid transfer protein: Molecular insight into the possible mechanism of lipid uptake. Biochemistry 56:1785–1796

    Article  CAS  PubMed  Google Scholar 

  78. Sumi M, Makino A, Inaba T et al (2017) Photoswitchable phospholipid FRET acceptor: detergent free intermembrane transfer assay of fluorescent lipid analogs. Sci Report 7:e2900

    Article  CAS  Google Scholar 

  79. Hölttä-Vuori M, Uronen R-L, Repakova J et al (2008) BODIPY-Cholesterol: A new tool to visualize sterol trafficking in living cells and organisms. Traffic 9:1839–1849

    Article  PubMed  CAS  Google Scholar 

  80. Locatelli-Hoops S, Remmel N, Klingenstein R et al (2006) Saposin a mobilizes lipids from low cholesterol and high bis(monoacylglycerol)phosphate-containing membranes: Patient variant saposin A lacks lipid extraction capacity. J Biol Chem 281:32451–32460

    Article  CAS  PubMed  Google Scholar 

  81. Kernstock RM, Girotti AW (2007) Lipid transfer protein binding of unmodified natural lipids as assessed by surface plasmon resonance methodology. Anal Biochem 365:111–121

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  82. Sugiki T, Takahashi H, Nagasu M et al (2010) Real-time assay method of lipid extraction activity. Anal Biochem 399:162–167

    Article  CAS  PubMed  Google Scholar 

  83. Ohvo-Rekilä H, Mattjus P (2011) Monitoring glycolipid transfer protein activity and membrane interaction with the surface plasmon resonance technique. Biochim Biophys Acta 1808:47–54

    Article  PubMed  CAS  Google Scholar 

  84. Davison JM, Bankaitis VA, Ghosh R (2012) Devising powerful genetics, biochemical and structural tools in the functional analysis of phosphatidylinositol transfer proteins (PITPs) across diverse species. Methods Cell Biol 108:249–302

    Article  CAS  PubMed  Google Scholar 

  85. Hanada K, Sugiki T (2017) In vitro assay to extract specific lipid types from phospholipid membranes using lipid-transfer proteins: a lesson from the ceramide transport protein CERT. In: Wood P (ed) Lipidomics, Neuromethods, vol 125. Humana Press, New York, NY

    Chapter  Google Scholar 

  86. Zhai X, Malakhova ML, Pike HP et al (2009) Glycolipid acquisition by human glycolipid transfer Protein dramatically alters intrinsic tryptophan fluorescence: Insights into glycolipid binding affinity. J Biol Chem 284:13620–13628

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  87. Kamlekar RK, Gao Y-G, Kenoth R et al (2010) Human GLTP: three distinct functions for the three tryptophans in a novel peripheral amphitropic fold. Biophys J 99:2626–2635

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  88. Kenoth R, Zou X, Simanshu DK et al (2018) Functional evaluation of tryptophans in glycolipid binding and membrane interaction by HET-C2, a fungal glycolipid transfer protein. BBA-Biomembranes 1860:1069–1076

    Article  CAS  PubMed  Google Scholar 

  89. Zhai X, Momsen WE, Malakhov DA et al (2013) GLTP-fold interaction with planar phosphatidylcholine surfaces is synergistically stimulated by phosphatidic acid and phosphatidylethanolamine. J Lipid Res 54:1103–1113

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  90. Kremer JM, Esker MW, Pathmamanoharan C, Wiersema PH (1977) Vesicles of variable diameter prepared by a modified injection method. Biochemistry 16:3932–3935

    Article  CAS  PubMed  Google Scholar 

  91. Nordlund JR, Schmidt CF, Dicken SN et al (1981) Transbilayer distribution of phosphatidylethanolamine in large and small unilamellar vesicles. Biochemistry 20:3237–3241

    Article  CAS  PubMed  Google Scholar 

  92. Schwarzmann G, Breiden B, Sandhoff K (2015) Membrane-spanning lipids for an uncompromised monitoring of membrane fusion and intermembrane lipid transfer. J Lipid Res 56:1861–1879

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Coldren B, van Zanten R, Mackel MJ et al (2003) From vesicle size distributions to bilayer elasticity via cryo-transmission and freeze-fracture electron microscopy. Langmuir 19:5632–5639

    Article  CAS  Google Scholar 

  94. Meister A, Blume A (2017) (Cryo)transmission electron microscopy of phospholipid model membranes interacting with amphiphilic and polyphilic molecules. Polymers 9:521

    Article  CAS  PubMed Central  Google Scholar 

  95. Edqvist J, Rönnberg E, Rosenquist S et al (2004) Plants express a lipid transfer protein with high similarity to mammalian sterol carrier protein-2. J Biol Chem 279:53544–53553

    Article  CAS  PubMed  Google Scholar 

  96. Wetterau JR, Zilversmit DB (1984) Quantitation of lipid transfer activity. Methods Biochem Anal 30:199–226

    CAS  PubMed  Google Scholar 

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Acknowledgments

We are grateful to many individuals who contributed to the development of the experimental approaches used routinely in the REB lab for many years and detailed here. They include J.G. Molotkovsky, H.M. Pike, X Zhai, I.A. Boldyrev, Y-G Gao, and P. Mattjus. We also are grateful for support from Dept. of Science and Technology, Science and Engineering Research Board (SERB), Govt. of India to RKK (YSS/2014/000021) and to RK (YSS/2015/000783) as well as support by NIH/NIGMS-GM45928, NIH/NCI-CA121493, and NIH/NHLBI-HL125353 (to REB) and the Hormel Foundation. We thank VIT for research facilities and infrastructure.

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Correspondence to Rhoderick E. Brown or Ravi Kanth Kamlekar .

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Kenoth, R., Brown, R.E., Kamlekar, R.K. (2019). In Vitro Measurement of Sphingolipid Intermembrane Transport Illustrated by GLTP Superfamily Members. In: Drin, G. (eds) Intracellular Lipid Transport. Methods in Molecular Biology, vol 1949. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-9136-5_17

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