Abstract
Transbilayer migration of membrane phospholipid arising from membrane insertion of the terminal human complement proteins has been investigated. Asymmetric vesicles containing pyrene-labeled phosphatidylcholine (pyrenePC) concentrated in the inner monolayer were prepared by outer monolayer exchange between pyrenePC-containing large unilamellar vesicles and excess (unlabeled) small unilamellar vesicles, using bovine liver phosphatidylcholine-specific exchange protein. After depletion of pyrenePC from the outer monolayer, the asymmetric large unilamellar vesicles were isolated by gel filtration and exposed to the purified C5b-9 proteins at 37 degrees C. Transbilayer exchange of phospholipid between inner and outer monolayers during C5b-9 assembly was monitored by changes in pyrene excimer and monomer fluorescence. Membrane deposition of the C5b67 complex (by incubation with C5b6 + C7) caused no change in pyrenePC fluorescence. Addition of C8 to the C5b67 vesicles resulted in a dose-dependent decrease in the excimer/monomer ratio. This change was observed both in the presence and absence of complement C9. No change in fluorescence was observed for control vesicles exposed to C8 (in the absence of membrane C5b67), or upon C5b-9 addition to vesicles containing pyrenePC symmetrically distributed between inner and outer monolayers. These data suggest that a transbilayer exchange of phospholipid between inner and outer monolayers is initiated upon C8 binding to C5b67. The fluorescence data were analyzed according to a "random walk" model for excimer formation developed for the case where pyrenePC is asymmetrically distributed between lipid bilayers. Based on this analysis, we estimate that a net transbilayer migration of approximately 1% of total membrane phospholipid is initiated upon C8 binding to C5b67. The potential significance of this transbilayer exchange of membrane phospholipid to the biological activity of the terminal complement proteins is considered.
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Selected References
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- Ando B., Wiedmer T., Hamilton K. K., Sims P. J. Complement proteins C5b-9 initiate secretion of platelet storage granules without increased binding of fibrinogen or von Willebrand factor to newly expressed cell surface GPIIb-IIIa. J Biol Chem. 1988 Aug 25;263(24):11907–11914. [PubMed] [Google Scholar]
- BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
- Barenholz Y., Gibbes D., Litman B. J., Goll J., Thompson T. E., Carlson R. D. A simple method for the preparation of homogeneous phospholipid vesicles. Biochemistry. 1977 Jun 14;16(12):2806–2810. doi: 10.1021/bi00631a035. [DOI] [PubMed] [Google Scholar]
- Bevers E. M., Comfurius P., Zwaal R. F. Changes in membrane phospholipid distribution during platelet activation. Biochim Biophys Acta. 1983 Dec 7;736(1):57–66. doi: 10.1016/0005-2736(83)90169-4. [DOI] [PubMed] [Google Scholar]
- Bretscher M. S. Phosphatidyl-ethanolamine: differential labelling in intact cells and cell ghosts of human erythrocytes by a membrane-impermeable reagent. J Mol Biol. 1972 Nov 28;71(3):523–528. doi: 10.1016/s0022-2836(72)80020-2. [DOI] [PubMed] [Google Scholar]
- Brown R. E., Stephenson F. A., Markello T., Barenholz Y., Thompson T. E. Properties of a specific glycolipid transfer protein from bovine brain. Chem Phys Lipids. 1985 Aug 30;38(1-2):79–93. doi: 10.1016/0009-3084(85)90059-3. [DOI] [PubMed] [Google Scholar]
- Classen J., Haest C. W., Tournois H., Deuticke B. Gramicidin-induced enhancement of transbilayer reorientation of lipids in the erythrocyte membrane. Biochemistry. 1987 Oct 20;26(21):6604–6612. doi: 10.1021/bi00395a007. [DOI] [PubMed] [Google Scholar]
- Comfurius P., Bevers E. M., Zwaal R. F. The involvement of cytoskeleton in the regulation of transbilayer movement of phospholipids in human blood platelets. Biochim Biophys Acta. 1985 Apr 26;815(1):143–148. doi: 10.1016/0005-2736(85)90485-7. [DOI] [PubMed] [Google Scholar]
- Correa-Freire M. C., Barenholz Y., Thompson T. E. Glucocerebroside transfer between phosphatidylcholine bilayers. Biochemistry. 1982 Mar 16;21(6):1244–1248. doi: 10.1021/bi00535a021. [DOI] [PubMed] [Google Scholar]
- Cullis P. R., De Kruijff B. Polymorphic phase behaviour of lipid mixtures as detected by 31P NMR. Evidence that cholesterol may destabilize bilayer structure in membrane systems containing phosphatidylethanolamine. Biochim Biophys Acta. 1978 Feb 21;507(2):207–218. doi: 10.1016/0005-2736(78)90417-0. [DOI] [PubMed] [Google Scholar]
- Dankert J. R., Shiver J. W., Esser A. F. Ninth component of complement: self-aggregation and interaction with lipids. Biochemistry. 1985 May 21;24(11):2754–2762. doi: 10.1021/bi00332a024. [DOI] [PubMed] [Google Scholar]
- Eisinger J., Flores J. Cytosol-membrane interface of human erythrocytes. A resonance energy transfer study. Biophys J. 1983 Mar;41(3):367–379. doi: 10.1016/S0006-3495(83)84448-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisinger J., Flores J., Petersen W. P. A milling crowd model for local and long-range obstructed lateral diffusion. Mobility of excimeric probes in the membrane of intact erythrocytes. Biophys J. 1986 May;49(5):987–1001. doi: 10.1016/S0006-3495(86)83727-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Esser A. F., Kolb W. P., Podack E. R., Müller-Eberhard H. J. Molecular reorganization of lipid bilayers by complement: a possible mechanism for membranolysis. Proc Natl Acad Sci U S A. 1979 Mar;76(3):1410–1414. doi: 10.1073/pnas.76.3.1410. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Everett J., Zlotnick A., Tennyson J., Holloway P. W. Fluorescence quenching of cytochrome b5 in vesicles with an asymmetric transbilayer distribution of brominated phosphatidylcholine. J Biol Chem. 1986 May 25;261(15):6725–6729. [PubMed] [Google Scholar]
- Galla H. J., Hartmann W. Excimer-forming lipids in membrane research. Chem Phys Lipids. 1980 Oct;27(3):199–219. doi: 10.1016/0009-3084(80)90036-5. [DOI] [PubMed] [Google Scholar]
- Galla H. J., Hartmann W., Theilen U., Sackmann E. On two-dimensional passive random walk in lipid bilayers and fluid pathways in biomembranes. J Membr Biol. 1979 Jul 31;48(3):215–236. doi: 10.1007/BF01872892. [DOI] [PubMed] [Google Scholar]
- Gazitt Y., Ohad I., Loyter A. Changes in phosoholipid susceptibility toward phospholipases induced by ATP depletion in avian and amphibian erythrocyte membranes. Biochim Biophys Acta. 1975 Feb 28;382(1):65–72. doi: 10.1016/0005-2736(75)90373-9. [DOI] [PubMed] [Google Scholar]
- Haest C. W., Deuticke B. Experimental alteration of phospholipid-protein interactions within the human erythrocyte membrane. Dependence on glycolytic metabolism. Biochim Biophys Acta. 1975 Sep 2;401(3):468–480. doi: 10.1016/0005-2736(75)90244-8. [DOI] [PubMed] [Google Scholar]
- Hattori R., Hamilton K. K., McEver R. P., Sims P. J. Complement proteins C5b-9 induce secretion of high molecular weight multimers of endothelial von Willebrand factor and translocation of granule membrane protein GMP-140 to the cell surface. J Biol Chem. 1989 May 25;264(15):9053–9060. [PubMed] [Google Scholar]
- Haxby J. A., Götze O., Müller-Eberhard H. J., Kinsky S. C. Release of trapped marker from liposomes by the action of purified complement components. Proc Natl Acad Sci U S A. 1969 Sep;64(1):290–295. doi: 10.1073/pnas.64.1.290. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hu V. W., Esser A. F., Podack E. R., Wisnieski B. J. The membrane attack mechanism of complement: photolabeling reveals insertion of terminal proteins into target membrane. J Immunol. 1981 Jul;127(1):380–386. [PubMed] [Google Scholar]
- Hänsch G. M., Gemsa D., Resch K. Induction of prostanoid synthesis in human platelets by the late complement components C5b-9 and channel forming antibiotic nystatin: inhibition of the reacylation of liberated arachidonic acid. J Immunol. 1985 Aug;135(2):1320–1324. [PubMed] [Google Scholar]
- Jackson M. L., Litman B. J. Rhodopsin-phospholipid reconstitution by dialysis removal of octyl glucoside. Biochemistry. 1982 Oct 26;21(22):5601–5608. doi: 10.1021/bi00265a033. [DOI] [PubMed] [Google Scholar]
- Kornberg R. D., McConnell H. M. Inside-outside transitions of phospholipids in vesicle membranes. Biochemistry. 1971 Mar 30;10(7):1111–1120. doi: 10.1021/bi00783a003. [DOI] [PubMed] [Google Scholar]
- Lupu F., Calb M., Fixman A. Alterations of phospholipid asymmetry in the membrane of spontaneously aggregated platelets in diabetes. Thromb Res. 1988 Jun 1;50(5):605–616. doi: 10.1016/0049-3848(88)90319-2. [DOI] [PubMed] [Google Scholar]
- Michaels D. W., Abramovitz A. S., Hammer C. H., Mayer M. M. Increased ion permeability of planar lipid bilayer membranes after treatment with the C5b-9 cytolytic attack mechanism of complement. Proc Natl Acad Sci U S A. 1976 Aug;73(8):2852–2856. doi: 10.1073/pnas.73.8.2852. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Müller-Eberhard H. J. The membrane attack complex. Springer Semin Immunopathol. 1984;7(2-3):93–141. doi: 10.1007/BF01893017. [DOI] [PubMed] [Google Scholar]
- Podack E. R., Biesecker G., Müller-Eberhard H. J. Membrane attack complex of complement: generation of high-affinity phospholipid binding sites by fusion of five hydrophilic plasma proteins. Proc Natl Acad Sci U S A. 1979 Feb;76(2):897–901. doi: 10.1073/pnas.76.2.897. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Podack E. R., Stoffel W., Esser A. F., Müller-Eberhard H. J. Membrane attack complex of complement: distribution of subunits between the hydrocarbon phase of target membranes and water. Proc Natl Acad Sci U S A. 1981 Jul;78(7):4544–4548. doi: 10.1073/pnas.78.7.4544. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sandberg H., Bode A. P., Dombrose F. A., Hoechli M., Lentz B. R. Expression of coagulant activity in human platelets: release of membranous vesicles providing platelet factor 1 and platelet factor 3. Thromb Res. 1985 Jul 1;39(1):63–79. doi: 10.1016/0049-3848(85)90122-7. [DOI] [PubMed] [Google Scholar]
- Sims P. J. Complement pores in erythrocyte membranes. Analysis of C8/C9 binding required for functional membrane damage. Biochim Biophys Acta. 1983 Aug 10;732(3):541–552. doi: 10.1016/0005-2736(83)90230-4. [DOI] [PubMed] [Google Scholar]
- Sims P. J. Complement protein C9 labeled with fluorescein isothiocyanate can be used to monitor C9 polymerization and formation of the cytolytic membrane lesion. Biochemistry. 1984 Jul 3;23(14):3248–3260. doi: 10.1021/bi00309a020. [DOI] [PubMed] [Google Scholar]
- Sims P. J., Faioni E. M., Wiedmer T., Shattil S. J. Complement proteins C5b-9 cause release of membrane vesicles from the platelet surface that are enriched in the membrane receptor for coagulation factor Va and express prothrombinase activity. J Biol Chem. 1988 Dec 5;263(34):18205–18212. [PubMed] [Google Scholar]
- Sims P. J. Permeability characteristics of complement-damaged membranes: evaluation of the membrane leak generated by the complement proteins C5b-9. Proc Natl Acad Sci U S A. 1981 Mar;78(3):1838–1842. doi: 10.1073/pnas.78.3.1838. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sims P. J., Wiedmer T. Kinetics of polymerization of a fluoresceinated derivative of complement protein C9 by the membrane-bound complex of complement proteins C5b-8. Biochemistry. 1984 Jul 3;23(14):3260–3267. doi: 10.1021/bi00309a021. [DOI] [PubMed] [Google Scholar]
- Sims P. J., Wiedmer T. The influence of electrochemical gradients of Na+ and K+ upon the membrane binding and pore forming activity of the terminal complement proteins. J Membr Biol. 1984;78(2):169–176. doi: 10.1007/BF01869204. [DOI] [PubMed] [Google Scholar]
- Steckel E. W., Welbaum B. E., Sodetz J. M. Evidence of direct insertion of terminal complement proteins into cell membrane bilayers during cytolysis. Labeling by a photosensitive membrane probe reveals a major role for the eighth and ninth components. J Biol Chem. 1983 Apr 10;258(7):4318–4324. [PubMed] [Google Scholar]
- Tschopp J., Podack E. R., Müller-Eberhard H. J. The membrane attack complex of complement: C5b-8 complex as accelerator of C9 polymerization. J Immunol. 1985 Jan;134(1):495–499. [PubMed] [Google Scholar]
- Vodyanoy I., Hall J. E., Balasubramanian T. M. Alamethicin-induced current-voltage curve asymmetry in lipid bilayers. Biophys J. 1983 Apr;42(1):71–82. doi: 10.1016/S0006-3495(83)84370-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wiedmer T., Ando B., Sims P. J. Complement C5b-9-stimulated platelet secretion is associated with a Ca2+-initiated activation of cellular protein kinases. J Biol Chem. 1987 Oct 5;262(28):13674–13681. [PubMed] [Google Scholar]
- Wiedmer T., Esmon C. T., Sims P. J. Complement proteins C5b-9 stimulate procoagulant activity through platelet prothrombinase. Blood. 1986 Oct;68(4):875–880. [PubMed] [Google Scholar]
- Wiedmer T., Esmon C. T., Sims P. J. On the mechanism by which complement proteins C5b-9 increase platelet prothrombinase activity. J Biol Chem. 1986 Nov 5;261(31):14587–14592. [PubMed] [Google Scholar]
- Wiedmer T., Sims P. J. Effect of complement proteins C5b-9 on blood platelets. Evidence for reversible depolarization of membrane potential. J Biol Chem. 1985 Jul 5;260(13):8014–8019. [PubMed] [Google Scholar]
- Zwaal R. F., Roelofsen B., Colley C. M. Localization of red cell membrane constituents. Biochim Biophys Acta. 1973 Sep 10;300(2):159–182. doi: 10.1016/0304-4157(73)90003-8. [DOI] [PubMed] [Google Scholar]
- van den Zegel M., Boens N., de Schryver F. C. Fluorescence decay of 1-methylpyrene in small unilamellar l-alpha-dimyristoylphosphatidylcholine vesicles. A temperature and concentration dependence study. Biophys Chem. 1984 Nov;20(4):333–345. doi: 10.1016/0301-4622(84)80023-x. [DOI] [PubMed] [Google Scholar]
