The self-organization of lipids and proteins of myelin at the membrane interface. Molecular factors underlying the microheterogeneity of domain segregation

Biochimica et Biophysica Acta - Biomembranes

Volumn 1778, Issue 7-8, 2008, Pages 1665-1675

  Rosetti, Carla M ^a   Maggio, Bruno ^a   Oliveira, Rafael G ^a  

^a UNIVERSIDAD NACIONAL DE CÓRDOBA   (Argentina)

Author keywords

Biomembranes; Folch Lees proteolipid; Langmuir monolayers; Lipid protein domains; Myelin; Myelin basic protein

Indexed keywords

CHOLESTEROL; GALACTOSYLCERAMIDE; GANGLIOSIDE GM1; LIPID; MYELIN; MYELIN PROTEIN; PHOSPHATIDYLSERINE; PROTEOLIPID;

LANGMUIR BLODGETT FILM; LIQUID PHASE MICROEXTRACTION; MEMBRANE; MOLECULAR WEIGHT; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN STRUCTURE; REVIEW;

EID: 45349095327     PISSN: 00052736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamem.2008.02.007     Document Type: Review

References (113)

1. Franklin B. On the stilling of waves by means of oil. Philos. Trans. R. Soc. London. 64 (1774) 445-460
2. Giles G.H., Forrester S.D., and Roberts G.G. Historical introduction. In: Roberts G.G. (Ed). Langmuir-Blodgett Films (1990), Plenum Press, New York
3. Bragg W.H., and Bragg W.L. X Rays and Crystal Structure (1924) New York
4. Rayleigh L. Proc. R. Soc. London. 47 (1890) 364
5. Langmuir I. The constitution and fundamental properties of solids and liquids. II Liquids. J. Am. Chem. Soc. 39 (1917) 1848-1906
6. Perrin J. Ann. Phys. x (1918) 160
7. Gorter E., and Grendel F. On bimolecular layers of lipoids on the chromocytes of the blood. J. Exp. Med. 41 (1925) 439-443
8. Gaines Jr. G.L. Insoluble Monolayers at Liquid-Gas Interfaces (1966), Interscience Publishers, New York
9. Möhwald H. Phospholipid and phospholipid-protein monolayers at the air/water interface. Annu. Rev. Phys. Chem. 41 (1990) 441-476
10. McConnell H.M. Structures and transitions in lipid monolayers at the air-water interface. Annu. Rev. Phys. Chem. 42 (1991) 171-195
11. Phillips M.C., and Chapman D. Monolayer characteristics of saturated 1,2,-diacyl phosphatidylcholines (lecithins) and phosphatidylethanolamines at the air-water interface. Biochim. Biophys. Acta. 163 (1968) 301-313
12. Vilallonga F. Surface of l-alpha-diphalmitoyl lecithin at the air-water interface. Biochim. Biophys. Acta. 163 (1968) 290-300
13. Albrecht O., Gruler H., and Sackmann E. Polymorphism of phospholipid monolayers. J. Phys. France. 39 (1978) 301-313
14. Leathes J.B. Role of fats in vital phenomena. Lancet 208 (1925) 853-856
15. Macritchie F. Proteins at interfaces. Adv. Protein. Chem. 32 (1978) 283-326
16. Brockman H. Lipid monolayers: why use half a membrane to characterize protein-membrane interactions?. Curr. Opin. Struct. Biol. 9 (1999) 438-443
17. Subramaniam S., and McConnell H.M. Critical mixing in monolayer mixtures of phospholipid and cholesterol. J. Phys. Chem. 91 (1987) 1715-1718
18. Gershfeld N.L. The critical unilamellar lipid state: a perspective for membrane bilayer assembly. Biochim. Biophys. Acta. 988 (1989) 335-350
19. Verger R., and Pattus F. Spreading of membranes at the air/water interface. Chem. Phys. Lipids. 16 (1976) 285-291
20. Pattus F., Piovant M.C., Lazdunski C.J., Desnuelle P., and Verger R. Spreading of biomembranes at the air/water interface. Biochim. Biophys. Acta. 507 (1978) 71-82
21. Pattus F., Rothen C., Streit M., and Zahler P. Structure, composition, enzymatic activities of human erythrocyte and sarcoplasmic reticulum membrane films. Biochim. Biophys. Acta. 647 (1981) 29-39
22. Schurholz T., and Schindler H. Lipid-protein surface films generated from membrane vesicles: selfassembly, composition, and film structure. Eur. Biophys. J. 20 (1991) 71-78
23. Calderon R.O., Maggio B., Neuberger T.J., and DeVries G.H. Modulation of Schwann cell Po glycoprotein and galactocerebroside by the surface organization of axolemma. J. Neurosci. Res. 40 (1995) 349-358
24. von Tscharner V., and McConnell H.M. An alternative view of phospholipid phase behavior at the air-water interface. Microscope and film balance studies. Biophys. J. 36 (1981) 409-419
25. Hénon S., and Meunier J. Microscope at the Brewster angle: direct observation of first-order phase transitions in monolayers. Rev. Sci. Instr. 62 (1991) 936-939
26. Hönig D., and Möbius D. Direct visualization of monolayers at the air-water interface by Brewster angle microscopy. J. Phys. Chem. 95 (1991) 4590-4592
27. Hönig D., and Möbius D. Reflectometry at the Brewster angle and Brewster angle microscopy at the air-water interface. Thin. Solid. Films. 210/211 (1992) 64-68
28. Rosetti C.M., Oliveira R.G., and Maggio B. Reflectance and topography of glycosphingolipid monolayers at the air-water interface. Langmuir 19 (2003) 377-384
29. Ducharme D., Tessier A., and Russev S.C. Simultaneous thickness and refractive index determination of monolayer deposited on an aqueous subphase by null ellipsometry. Langmuir 17 (2001) 7529-7534
30. Roberts G.G. Langmuir-Blodgett Films (1990), Plenum Press, New York
31. Oliveira R.G., and Maggio B. Compositional domain immiscibility in whole myelin monolayers at the air-water interface and Langmuir-Blodgett films. Biochim. Biophys. Acta. 1561 (2002) 238-250
32. Möbius D., and Miller R. Novel Methods to Study Interfacial Layers (2001), Elsevier Science, Amsterdam
33. Dynarowicz-Latka P., Dhanabalan A., and Oliveira Jr. O.N. Modern physicochemical research on Langmuir monolayers. Adv. Colloid. Interface. Sci. 91 (2001) 221-293
34. Folch J., and Lees M. Proteolipides, a new type of tissue lipoproteins; their isolation from brain. J. Biol. Chem. 191 (1951) 807-817
35. Kies M.W. Chemical studies on an encephalitogenic protein from Guinea pig brain. Annals. New. York. Acad. Sci. 122 (1965) 161-170
36. Gonzalez-Sastre F. The protein composition of isolated myelin. J. Neurochem. 17 (1970) 1049-1056
37. Discher B.M., Maloney K.M., Schief Jr. W.R., Grainger D.W., Vogel V., and Hall S.B. Lateral phase separation in interfacial films of pulmonary surfactant. Biophys. J. 71 (1996) 2583-2590
38. Nag K., Perez-Gil J., Ruano M.L., Worthman L.A., Stewart J., Casals C., and Keough K.M. Phase transitions in films of lung surfactant at the air-water interface. Biophys. J. 74 (1998) 2983-2995
39. Norton W.T., and Cammer W. Isolation and characterization of myelin. In: Pierre M. (Ed). Myelin (1984), Plenum Press, New York 147-195
40. Oliveira R.G., Calderon R.O., and Maggio B. Surface behavior of myelin monolayers. Biochim. Biophys. Acta. 1370 (1998) 127-137
41. Calderon R.O., Maggio B., Neuberger T.J., and De Vries G.H. Surface behavior of axolemma monolayers: physico-chemical characterization and use as supported planar membranes for cultured Schwann cells. J. Neurosci. Res. 34 (1993) 206-218
42. Trurnit H.J. J. Colloid. Sci. 15 (1960) 1-13
43. Fidelio G.D., Maggio B., and Cumar F.A. Interaction of soluble and membrane proteins with monolayers of glycosphingolipids. Biochem. J. 203 (1982) 717-725
44. Ginsberg L., and Gershfeld N.L. Membrane bilayer instability and the pathogenesis of disorders of myelin. Neurosci. Lett. 130 (1991) 133-136
45. Oliveira R.G., and Maggio B. Surface behavior, microheterogeneity and adsorption equilibrium of myelin at the air-water interface. Chem. Phys. Lipids. 122 (2003) 171-176
46. Hess M.W., Kirschning E., Pfaller K., Debbage P.L., Hohenberg H., and Klima G. 5000-year-old myelin: uniquely intact in molecular configuration and fine structure. Curr. Biol. 8 (1998) R512-R513
47. Caspar D.L., and Kirschner D.A. Myelin membrane structure at 10 Å resolution. Nat. New. Biol. 231 (1971) 46-52
48. Kirschner D.A., Ganser A.L., and Caspar D.L. Diffraction studies of molecular organization and membrane interactions in myelin. In: Pierre M. (Ed). Myelin (1984), Plenum Press, New York 51-95
49. Brown 3rd F.R., Karthigasan J., Singh I., and Kirschner D.A. X-ray diffraction analysis of myelin lipid/proteolipid protein multilayers. J. Neurosci. Res. 24 (1989) 192-200
50. Ruiz-Sanz J., Ruiz-Cabello J., Lopez-Mayorga O., Cortijo M., and Mateo P.L. Thermal stability of bovine-brain myelin membrane. Eur. Biophys. J. 21 (1992) 169-178
51. Oliveira R.G., and Maggio B. Epifluorescence microscopy of surface domain microheterogeneity in myelin monolayers at the air-water interface. Neurochem. Res. 25 (2000) 77-86
52. Keller S.L., Pitcher III W.H., Huestis W.H., and McConnell H.M. Red blood cell lipids form immiscible liquids. Phys. Rev. Lett. 81 (1998) 5019-5022
53. de la Serna J.B., Perez-Gil J., Simonsen A.C., and Bagatolli L.A. Cholesterol rules: direct observation of the coexistence of two fluid phases in native pulmonary surfactant membranes at physiological temperatures. J. Biol. Chem. 279 (2004) 40715-40722
54. Serrano A.G., and Perez-Gil J. Protein-lipid interactions and surface activity in the pulmonary surfactant system. Chem. Phys. Lipids. 141 (2006) 105-118
55. Dietrich C., Bagatolli L.A., Volovyk Z.N., Thompson N.L., Levi M., Jacobson K., and Gratton E. Lipid rafts reconstituted in model membranes. Biophys. J. 80 (2001) 1417-1428
56. Oliveira R.G., Tanaka M., and Maggio B. Many length scales surface fractality in monomolecular films of whole myelin lipids and proteins. J. Struct. Biol. 149 (2005) 158-169
57. Rosetti C.M., Oliveira R.G., and Maggio B. The Folch-Lees proteolipid induces phase coexistence and transverse reorganization of lateral domains in myelin monolayers. Biochim. Biophys. Acta. 1668 (2005) 75-86
58. Fidelio G.D., Maggio B., and Cumar F.A. Interaction of myelin basic protein, melittin and bovine serum albumin with gangliosides, sulphatide and neutral glycosphingolipids in mixed monolayers. Chem. Phys. Lipids. 35 (1984) 231-245
59. Rosetti C.M., and Maggio B. Protein-induced surface structuring in myelin membrane monolayers. Biophys. J. 93 (2007) 4254-4267
60. Maggio B., Cumar F.A., and Caputto R. Surface behaviour of gangliosides and related glycosphingolipids. Biochem. J. 171 (1978) 559-565
61. Demel R.A., Bruckdorfer K.R., and van Deenen L.L. Structural requirements of sterols for the interaction with lecithin at the air water interface. Biochim. Biophys. Acta. 255 (1972) 311-320
62. Demel R.A., Paltauf F., and Hauser H. Monolayer characteristics and thermal behavior of natural and synthetic phosphatidylserines. Biochemistry 26 (1987) 8659-8665
63. Maggio B. The surface behavior of glycosphingolipids in biomembranes: a new frontier of molecular ecology. Prog. Biophys. Mol. Biol. 62 (1994) 55-117
64. Leveiller F., Böhm C., Jacquemain D., Möhwald H., Leiserowitz L., Kjaer K., and Als-Nielsen J. Two-dimensional crystal structure of Cadmium Arachidate studied by synchrotron X-ray diffraction and reflectivity. Langmuir 10 (1994) 819-829
65. Boggs J.M. Lipid intermolecular hydrogen bonding: influence on structural organization and membrane function. Biochim. Biophys. Acta. 906 (1987) 353-404
66. Maggio B. Favorable and unfavorable lateral interactions of ceramide, neutral glycosphingolipids and gangliosides in mixed monolayers. Chem. Phys. Lipids. 132 (2004) 209-224
67. Silvius J.R., del Giudice D., and Lafleur M. Cholesterol at different bilayer concentrations can promote or antagonize lateral segregation of phospholipids of differing acyl chain length. Biochemistry 35 (1996) 15198-15208
68. Feigenson G.W. Phase boundaries and biological membranes. Annu. Rev. Biophys. Biomol. Struct. 36 (2007) 63-77
69. Regen S.L. Lipid-lipid recognition in fluid bilayers: solving the cholesterol mystery. Curr. Opin. Chem. Biol. 6 (2002) 729-735
70. Lange Y., D'Alessandro J.S., and Small D.M. The affinity of cholesterol for phosphatidylcholine and sphingomyelin. Biochim. Biophys. Acta. 556 (1979) 388-398
71. Ramstedt B., and Slotte J.P. Sphingolipids and the formation of sterol-enriched ordered membrane domains. Biochim. Biophys. Acta. 1758 (2006) 1945-1956
72. McConnell H.M., and Radhakrishnan A. Condensed complexes of cholesterol and phospholipids. Biochim. Biophys. Acta. 1610 (2003) 159-173
73. Somerharju P., Virtanen J.A., and Cheng K.H. Lateral organisation of membrane lipids. The superlattice view. Biochim. Biophys. Acta. 1440 (1999) 32-48
74. Bloom M., and Mouritsen O.G. The evolution of membranes. In: Hoff A.J. (Ed). Structure and Dynamics of Membranes Vol. 1A (1995), Elsevier, Amsterdam 65
75. McIntosh T.J., Simon S.A., Needham D., and Huang C.H. Structure and cohesive properties of sphingomyelin/cholesterol bilayers. Biochemistry 31 (1992) 2012-2020
76. Needham D., and Nunn R.S. Elastic deformation and failure of lipid bilayer membranes containing cholesterol. Biophys. J. 58 (1990) 997-1009
77. Vidal A., and McIntosh T.J. Transbilayer peptide sorting between raft and nonraft bilayers: comparisons of detergent extraction and confocal microscopy. Biophys. J. 89 (2005) 1102-1108
78. Epand R.M. Do proteins facilitate the formation of cholesterol-rich domains?. Biochim. Biophys. Acta. 1666 (2004) 227-238
79. Smaby J.M., Brockman H.L., and Brown R.E. Cholesterol's interfacial interactions with sphingomyelins and phosphatidylcholines: hydrocarbon chain structure determines the magnitude of condensation. Biochemistry 33 (1994) 9135-9142
80. Franks N.P., Melchior V., Kirshner D.A., and Caspar D.L. Structure of myelin lipid bilayers. Changes during maturation. J. Mol. Biol. 155 (1982) 133-153
81. Riccio P., Fasano A., Borenshtein N., Bleve-Zacheo T., and Kirschner D.A. Multilamellar packing of myelin modeled by lipid-bound MBP. J. Neurosci. Res. 59 (2000) 513-521
82. Finean J.B., and Hutchinson A.L. X-ray diffraction studies of lipid phase transitions in cholesterol-rich membranes at sub-zero temperatures. Chem. Phys. Lipids. 46 (1988) 63-71
83. Clarke J.A., Heron A.J., Seddon J.M., and Law R.V. The diversity of the liquid ordered (Lo) phase of phosphatidylcholine/cholesterol membranes: a variable temperature multinuclear solid-state NMR and X-ray diffraction study. Biophys. J. 90 (2006) 2383-2393
84. Chachaty C., Rainteau D., Tessier C., Quinn P.J., and Wolf C. Building up of the liquid-ordered phase formed by sphingomyelin and cholesterol. Biophys. J. 88 (2005) 4032-4044
85. Ayala G., Carmona P., de Cozar M., and Monreal J. Vibrational spectra and structure of myelin membranes. Eur. Biophys. J. 14 (1987) 219-225
86. Dewey T.G. Fractals in Molecular Biophysics (1997), Oxford University Press, Oxford
87. Miller A., Knoll W., and Mohwald H. Fractal growth of crystalline phospholipid domains in monomolecular layers. Phys. Rev. Lett. 56 (1986) 2633-2636
88. Poon W.C.K., and Haw M.D. Mesoscopic structure formation in colloidal aggregation and gelation. Advances. in. Colloid. an. Interface. Science. 73 (1997) 71-126
89. Maggio B., Sturtevant J.M., and Yu R.K. Effect of myelin basic protein on the thermotropic behavior of aqueous dispersions of neutral and anionic glycosphingolipids and their mixtures with dipalmitoylphosphatidylcholine. J. Biol. Chem. 262 (1987) 2652-2659
90. Sankaram M.B., Brophy P.J., and Marsh D. Spin-label ESR studies on the interaction of bovine spinal cord myelin basic protein with dimyristoylphosphatidylglycerol dispersions. Biochemistry 28 (1989) 9685-9691
91. Rosetti C.M., and Ph.D.D. Estructuracion lateral y topografica de dominios lipidicos segregados en el plano lateral de interfaces que contienen lipidos y proteinas (2008), Universidad Nacional de Cordoba, Cordoba, Argentina
92. Maggio B. Molecular interactions of the major myelin glycosphingolipids and myelin basic protein in model membranes. Neurochem. Res. 22 (1997) 475-481
93. Braun P.E. Molecular organization of myelin. In: Pierre M. (Ed). Myelin (1984), Plenum Press, New York 97-116
94. Maggio B., and Yu R.K. Modulation by glycosphingolipids of membrane-membrane interactions induced by myelin basic protein and melittin. Biochim. Biophys. Acta. 1112 (1992) 105-114
95. Boggs J.M., and Moscarello M.A. Structural organization of the human myelin membrane. Biochim. Biophys. Acta. 515 (1978) 1-21
96. Harauz G., Ishiyama N., Hill C.M., Bates I.R., Libich D.S., and Fares C. Myelin basic protein-diverse conformational states of an intrinsically unstructured protein and its roles in myelin assembly and multiple sclerosis. Micron 35 (2004) 503-542
97. McConnell H.M. Equilibration rates in lipid monolayers. Proc. Natl. Acad. Sci. U. S. A. 93 (1996) 15001-15003
98. Marsh D. Lateral pressure in membranes. Biochim. Biophys. Acta. 1286 (1996) 183-223
99. Phillips M.C., Graham D.E., and Hauser H. Lateral compressibility and penetration into phospholipid monolayers and bilayer membranes. Nature 254 (1975) 154-156
100. Feng S. Interpretation of mechanochemical properties of lipid bilayer vesicles from equation of state or pressure-area measurements of the monolayer at the air-water interface or oil-water interface. Langmuir 15 (1999) 998-1010
101. London Y., Demel R.A., Geurts van Kessel W.S., Vossenberg F.G., and van Deenen L.L. The protection of A1 myelin basic protein against the action of proteolytic enzymes after interaction of the protein with lipids at the air-water interface. Biochim. Biophys. Acta. 311 (1973) 520-530
102. da Silva P.P., and Miller R.G. Membrane particles on fracture faces of frozen myelin. Proc. Natl. Acad. Sci. U. S. A. 72 (1975) 4046-4050
103. Taylor C.M., Coetzee T., and Pfeiffer S.E. Detergent-insoluble glycosphingolipid/cholesterol microdomains of the myelin membrane. J. Neurochem. 81 (2002) 993-1004
104. Arvanitis D.N., Yang W., and Boggs J.M. Myelin proteolipid protein, basic protein, the small isoform of myelin-associated glycoprotein, and p42MAPK are associated in the Triton X-100 extract of central nervous system myelin. J. Neurosci. Res. 70 (2002) 8-23
105. Debruin L.S., and Harauz G. White matter rafting-membrane microdomains in myelin. Neurochem. Res. 32 (2007) 213-228
106. Gielen E., Baron W., Vandeven M., Steels P., Hoekstra D., and Ameloot M. Rafts in oligodendrocytes: evidence and structure-function relationship. Glia 54 (2006) 499-512
107. Joy R.T., and Finean J.B. A comparison of the effects of freezing and of treatment with hypertonic solutions on the structure of nerve myelin. J. Ultrastruct. Res. 8 (1963) 264-282
108. Lichtenberg D., Goni F.M., and Heerklotz H. Detergent-resistant membranes should not be identified with membrane rafts. Trends. Biochem. Sci. 30 (2005) 430-436
109. Heffer-Lauc M., Lauc G., Nimrichter L., Fromholt S.E., and Schnaar R.L. Membrane redistribution of gangliosides and glycosylphosphatidylinositol-anchored proteins in brain tissue sections under conditions of lipid raft isolation. Biochim. Biophys. Acta. 1686 3 (2005) 200-208
110. Munro S. Lipid rafts: elusive or illusive?. Cell 115 (2003) 377-388
111. McMullen T.P.W., Lewis R.N., and McElhaney R.N. Cholesterol-phospholipid interactions, the liquid-ordered phase and lipid rafts in model and biological membranes. Curr. Op. Colloid. Interface. Sci. 8 (2004) 459-468
112. Maggio B., Carrer D.C., Fanani M.L., Oliveira R.G., and Rosetti C.M. Interfacial behavior of glycosphingolipids and related sphingolipids. Curr. Op. Colloid. Interface. Sci. 8 (2004) 448-458
113. Maggio B., Fanani M.L., Rosetti C.M., and Wilke N. Biophysics of sphingolipids II. Glycosphingolipids: An assortment of multiple structural information transducers at the membrane surface. Biochim. Biophys. Acta. 1758 (2006) 1922-1944