Abstract
The fusion of large unilamellar phosphatidylserine liposomes (PS LUV) induced by La3+ has been monitored using the 1-aminoapthalene-3,6,8-trisulfonic acid/p-xylenebis(pyridinium bromide) (ANTS/DPX) fluorescence assay for the mixing of aqueous contents. The fusion event is extensive and nonleaky, with up to 95% mixing of contents in the fused liposomes. However, addition of excess EDTA leads to disruption of the fusion products in a way that implies the existence of metastable intermembrane contact sites. The maximal fusion activity occurs between 10 and 100 microM La3+ and fusion can be terminated rapidly, without loss of contents, by the addition of excess La3+, e.g., 1 mM La3+ at pH 7.4. This observation is explained by the very large intrinsic binding constant (approximately 10(5) M-1) of La3+ to the PS headgroup, as measured by microelectrophoresis. Addition of 1 mM La3+ causes charge reversal of the membrane and a large positive surface potential. La3+ binding to PS causes the release of a proton. These data can be explained if La3+ can chelate to PS at two sites, with one of the sites being the primary amino group. This binding model successfully predicts that at pH 4.5 fusion occurs up to 2 mM La3+, due to reduced La3+ binding at low pH. We conclude that the general mechanism of membrane fusion includes three kinetic steps. In addition to (a) aggregation, there is (b) the close approach of the surfaces, or thinning of the hydration layer, and (c) the formation of intermembrane intermediates which determine the extent to which membrane destabilization leads to fusion (mixing of aqueous contents), as opposed to lysis. The lifetime of these intermembrane intermediates appears to depend upon La3+ binding to both PS sites.
Full text
PDF














Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
- Bentz J., Düzgüneş N. Fusogenic capacities of divalent cations and effect of liposome size. Biochemistry. 1985 Sep 24;24(20):5436–5443. doi: 10.1021/bi00341a023. [DOI] [PubMed] [Google Scholar]
- Bentz J., Düzgüneş N., Nir S. Temperature dependence of divalent cation induced fusion of phosphatidylserine liposomes: evaluation of the kinetic rate constants. Biochemistry. 1985 Feb 12;24(4):1064–1072. doi: 10.1021/bi00325a039. [DOI] [PubMed] [Google Scholar]
- Bentz J., Ellens H., Lai M. Z., Szoka F. C., Jr On the correlation between HII phase and the contact-induced destabilization of phosphatidylethanolamine-containing membranes. Proc Natl Acad Sci U S A. 1985 Sep;82(17):5742–5745. doi: 10.1073/pnas.82.17.5742. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bentz J., Ellens H., Szoka F. C. Destabilization of phosphatidylethanolamine-containing liposomes: hexagonal phase and asymmetric membranes. Biochemistry. 1987 Apr 21;26(8):2105–2116. doi: 10.1021/bi00382a008. [DOI] [PubMed] [Google Scholar]
- Casal H. L., Mantsch H. H., Hauser H. Infrared studies of fully hydrated saturated phosphatidylserine bilayers. Effect of Li+ and Ca2+. Biochemistry. 1987 Jul 14;26(14):4408–4416. doi: 10.1021/bi00388a033. [DOI] [PubMed] [Google Scholar]
- Casal H. L., Martin A., Mantsch H. H., Paltauf F., Hauser H. Infrared studies of fully hydrated unsaturated phosphatidylserine bilayers. Effect of Li+ and Ca2+. Biochemistry. 1987 Nov 17;26(23):7395–7401. doi: 10.1021/bi00397a030. [DOI] [PubMed] [Google Scholar]
- Cevc G., Watts A., Marsh D. Titration of the phase transition of phosphatidylserine bilayer membranes. Effects of pH, surface electrostatics, ion binding, and head-group hydration. Biochemistry. 1981 Aug 18;20(17):4955–4965. doi: 10.1021/bi00520a023. [DOI] [PubMed] [Google Scholar]
- Cohen J. A., Cohen M. Adsorption of monovalent and divalent cations by phospholipid membranes. The monomer-dimer problem. Biophys J. 1981 Dec;36(3):623–651. doi: 10.1016/S0006-3495(81)84756-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cowley A. C., Fuller N. L., Rand R. P., Parsegian V. A. Measurement of repulsive forces between charged phospholipid bilayers. Biochemistry. 1978 Jul 25;17(15):3163–3168. doi: 10.1021/bi00608a034. [DOI] [PubMed] [Google Scholar]
- Curtis M. J., Quastel D. M., Saint D. A. Lanthanum as a surrogate for calcium in transmitter release at mouse motor nerve terminals. J Physiol. 1986 Apr;373:243–260. doi: 10.1113/jphysiol.1986.sp016045. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Deleers M., Servais J. P., Wülfert E. Micromolar concentrations of Al3+ induce phase separation, aggregation and dye release in phosphatidylserine-containing lipid vesicles. Biochim Biophys Acta. 1985 Mar 14;813(2):195–200. doi: 10.1016/0005-2736(85)90233-0. [DOI] [PubMed] [Google Scholar]
- Düzgünes N., Nir S., Wilschut J., Bentz J., Newton C., Portis A., Papahadjopoulos D. Calcium- and magnesium-induced fusion of mixed phosphatidylserine/phosphatidylcholine vesicles: effect of ion binding. J Membr Biol. 1981 Apr 15;59(2):115–125. doi: 10.1007/BF01875709. [DOI] [PubMed] [Google Scholar]
- Düzgüneş N., Allen T. M., Fedor J., Papahadjopoulos D. Lipid mixing during membrane aggregation and fusion: why fusion assays disagree. Biochemistry. 1987 Dec 15;26(25):8435–8442. doi: 10.1021/bi00399a061. [DOI] [PubMed] [Google Scholar]
- Düzgüneş N., Straubinger R. M., Baldwin P. A., Friend D. S., Papahadjopoulos D. Proton-induced fusion of oleic acid-phosphatidylethanolamine liposomes. Biochemistry. 1985 Jun 18;24(13):3091–3098. doi: 10.1021/bi00334a004. [DOI] [PubMed] [Google Scholar]
- Eisenberg M., Gresalfi T., Riccio T., McLaughlin S. Adsorption of monovalent cations to bilayer membranes containing negative phospholipids. Biochemistry. 1979 Nov 13;18(23):5213–5223. doi: 10.1021/bi00590a028. [DOI] [PubMed] [Google Scholar]
- Ellens H., Bentz J., Szoka F. C. Destabilization of phosphatidylethanolamine liposomes at the hexagonal phase transition temperature. Biochemistry. 1986 Jan 28;25(2):285–294. doi: 10.1021/bi00350a001. [DOI] [PubMed] [Google Scholar]
- Ellens H., Bentz J., Szoka F. C. Fusion of phosphatidylethanolamine-containing liposomes and mechanism of the L alpha-HII phase transition. Biochemistry. 1986 Jul 15;25(14):4141–4147. doi: 10.1021/bi00362a023. [DOI] [PubMed] [Google Scholar]
- Ellens H., Bentz J., Szoka F. C. H+- and Ca2+-induced fusion and destabilization of liposomes. Biochemistry. 1985 Jun 18;24(13):3099–3106. doi: 10.1021/bi00334a005. [DOI] [PubMed] [Google Scholar]
- Ellens H., Bentz J., Szoka F. C. pH-induced destabilization of phosphatidylethanolamine-containing liposomes: role of bilayer contact. Biochemistry. 1984 Mar 27;23(7):1532–1538. doi: 10.1021/bi00302a029. [DOI] [PubMed] [Google Scholar]
- Evans E. A., Parsegian V. A. Energetics of membrane deformation and adhesion in cell and vesicle aggregation. Ann N Y Acad Sci. 1983;416:13–33. doi: 10.1111/j.1749-6632.1983.tb35176.x. [DOI] [PubMed] [Google Scholar]
- Evans E. A., Parsegian V. A. Thermal-mechanical fluctuations enhance repulsion between bimolecular layers. Proc Natl Acad Sci U S A. 1986 Oct;83(19):7132–7136. doi: 10.1073/pnas.83.19.7132. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Evans E., Needham D. Giant vesicle bilayers composed of mixtures of lipids, cholesterol and polypeptides. Thermomechanical and (mutual) adherence properties. Faraday Discuss Chem Soc. 1986;(81):267–280. doi: 10.1039/dc9868100267. [DOI] [PubMed] [Google Scholar]
- Grasdalen H., Göran Eriksson L. E., Westman J., Ehrenberg A. Surface potential effects on metal ion binding to phosphatidylcholine membranes 31P NMR study of lanthanide and calcium ion binding to egg-yolk lecithin vesicles. Biochim Biophys Acta. 1977 Sep 5;469(2):151–162. doi: 10.1016/0005-2736(77)90177-8. [DOI] [PubMed] [Google Scholar]
- Hammoudah M. M., Nir S., Bentz J., Mayhew E., Stewart T. P., Hui S. W., Kurland R. J. Interactions of La2+ with phosphatidylserine vesicles: binding, phase transition, leakage, 31P-NMR and fusion. Biochim Biophys Acta. 1981 Jul 6;645(1):102–114. doi: 10.1016/0005-2736(81)90517-4. [DOI] [PubMed] [Google Scholar]
- Hauser H., Hinckley C. C., Krebs J., Levine B. A., Phillips M. C., Williams R. J. The interaction of ions with phosphatidylcholine. Biochim Biophys Acta. 1977 Aug 1;468(3):364–377. doi: 10.1016/0005-2736(77)90288-7. [DOI] [PubMed] [Google Scholar]
- Heuser J., Miledi R. Effects of lanthanum ions on function and structure of frog neuromuscular junctions. Proc R Soc Lond B Biol Sci. 1971 Dec 14;179(1056):247–260. doi: 10.1098/rspb.1971.0096. [DOI] [PubMed] [Google Scholar]
- Kachar B., Fuller N., Rand R. P. Morphological responses to calcium-induced interaction of phosphatidylserine-containing vesicles. Biophys J. 1986 Nov;50(5):779–788. doi: 10.1016/S0006-3495(86)83518-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LETTVIN J. Y., PICKARD W. F., MCCULLOCH W. S., PITTS W. A THEORY OF PASSIVE ION FLUX THROUGH AXON MEMBRANES. Nature. 1964 Jun 27;202:1338–1339. doi: 10.1038/2021338a0. [DOI] [PubMed] [Google Scholar]
- LeNeveu D. M., Rand R. P. Measurement and modification of forces between lecithin bilayers. Biophys J. 1977 May;18(2):209–230. doi: 10.1016/S0006-3495(77)85608-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LeNeveu D. M., Rand R. P., Parsegian V. A. Measurement of forces between lecithin bilayers. Nature. 1976 Feb 19;259(5544):601–603. doi: 10.1038/259601a0. [DOI] [PubMed] [Google Scholar]
- Leventis R., Gagné J., Fuller N., Rand R. P., Silvius J. R. Divalent cation induced fusion and lipid lateral segregation in phosphatidylcholine-phosphatidic acid vesicles. Biochemistry. 1986 Nov 4;25(22):6978–6987. doi: 10.1021/bi00370a600. [DOI] [PubMed] [Google Scholar]
- Lis L. J., McAlister M., Fuller N., Rand R. P., Parsegian V. A. Interactions between neutral phospholipid bilayer membranes. Biophys J. 1982 Mar;37(3):657–665. [PMC free article] [PubMed] [Google Scholar]
- Lis L. J., Parsegian V. A., Rand R. P. Binding of divalent cations of dipalmitoylphosphatidylcholine bilayers and its effect on bilayer interaction. Biochemistry. 1981 Mar 31;20(7):1761–1770. doi: 10.1021/bi00510a009. [DOI] [PubMed] [Google Scholar]
- Loosley-Millman M. E., Rand R. P., Parsegian V. A. Effects of monovalent ion binding and screening on measured electrostatic forces between charged phospholipid bilayers. Biophys J. 1982 Dec;40(3):221–232. doi: 10.1016/S0006-3495(82)84477-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MacDonald R. C., Simon S. A., Baer E. Ionic influences on the phase transition of dipalmitoylphosphatidylserine. Biochemistry. 1976 Feb 24;15(4):885–891. doi: 10.1021/bi00649a025. [DOI] [PubMed] [Google Scholar]
- Marra J. Direct measurement of the interaction between phosphatidylglycerol bilayers in aqueous electrolyte solutions. Biophys J. 1986 Nov;50(5):815–825. doi: 10.1016/S0006-3495(86)83522-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marra J., Israelachvili J. Direct measurements of forces between phosphatidylcholine and phosphatidylethanolamine bilayers in aqueous electrolyte solutions. Biochemistry. 1985 Aug 13;24(17):4608–4618. doi: 10.1021/bi00338a020. [DOI] [PubMed] [Google Scholar]
- McLaughlin A., Eng W. K., Vaio G., Wilson T., McLaughlin S. Dimethonium, a divalent cation that exerts only a screening effect on the electrostatic potential adjacent to negatively charged phospholipid bilayer membranes. J Membr Biol. 1983;76(2):183–193. doi: 10.1007/BF02000618. [DOI] [PubMed] [Google Scholar]
- McLaughlin S., Mulrine N., Gresalfi T., Vaio G., McLaughlin A. Adsorption of divalent cations to bilayer membranes containing phosphatidylserine. J Gen Physiol. 1981 Apr;77(4):445–473. doi: 10.1085/jgp.77.4.445. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mead R. H., Clusin W. T. Paradoxical electromechanical effect of lanthanum ions in cardiac muscle cells. Biophys J. 1985 Nov;48(5):695–700. doi: 10.1016/S0006-3495(85)83827-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Meers P., Hong K., Bentz J., Papahadjopoulos D. Spermine as a modulator of membrane fusion: interactions with acidic phospholipids. Biochemistry. 1986 Jun 3;25(11):3109–3118. doi: 10.1021/bi00359a007. [DOI] [PubMed] [Google Scholar]
- Miller D. C., Dahl G. P. Early events in calcium-induced liposome fusion. Biochim Biophys Acta. 1982 Jul 14;689(1):165–169. doi: 10.1016/0005-2736(82)90201-2. [DOI] [PubMed] [Google Scholar]
- Nir S., Bentz J., Wilschut J. Mass action kinetics of phosphatidylserine vesicle fusion as monitored by coalescence of internal vesicle volumes. Biochemistry. 1980 Dec 23;19(26):6030–6036. doi: 10.1021/bi00567a013. [DOI] [PubMed] [Google Scholar]
- Nir S., Düzgüneş N., Bentz J. Binding of monovalent cations to phosphatidylserine and modulation of Ca2+- and Mg2+-induced vesicle fusion. Biochim Biophys Acta. 1983 Oct 26;735(1):160–172. doi: 10.1016/0005-2736(83)90271-7. [DOI] [PubMed] [Google Scholar]
- Nir S., Wilschut J., Bentz J. The rate of fusion of phospholipid vesicles and the role of bilayer curvature. Biochim Biophys Acta. 1982 May 21;688(1):275–278. doi: 10.1016/0005-2736(82)90604-6. [DOI] [PubMed] [Google Scholar]
- Ohki S. A mechanism of divalent ion-induced phosphatidylserine membrane fusion. Biochim Biophys Acta. 1982 Jul 14;689(1):1–11. doi: 10.1016/0005-2736(82)90182-1. [DOI] [PubMed] [Google Scholar]
- Ohki S., Duax J. Effects of cations and polyamines on the aggregation and fusion of phosphatidylserine membranes. Biochim Biophys Acta. 1986 Sep 25;861(1):177–186. doi: 10.1016/0005-2736(86)90577-8. [DOI] [PubMed] [Google Scholar]
- Ohki S. Effects of divalent cations, temperature, osmotic pressure gradient, and vesicle curvature on phosphatidylserine vesicle fusion. J Membr Biol. 1984;77(3):265–275. doi: 10.1007/BF01870574. [DOI] [PubMed] [Google Scholar]
- Ohki S., Kurland R. Surface potential of phosphatidylserine monolayers. II. Divalent and monovalent ion binding. Biochim Biophys Acta. 1981 Jul 20;645(2):170–176. doi: 10.1016/0005-2736(81)90187-5. [DOI] [PubMed] [Google Scholar]
- Ohki S., Ohshima H. Divalent cation-induced phosphatidic acid membrane fusion. Effect of ion binding and membrane surface tension. Biochim Biophys Acta. 1985 Jan 10;812(1):147–154. doi: 10.1016/0005-2736(85)90532-2. [DOI] [PubMed] [Google Scholar]
- Papahadjopoulos D. Surface properties of acidic phospholipids: interaction of monolayers and hydrated liquid crystals with uni- and bi-valent metal ions. Biochim Biophys Acta. 1968 Sep 17;163(2):240–254. doi: 10.1016/0005-2736(68)90103-x. [DOI] [PubMed] [Google Scholar]
- Parsegian V. A., Fuller N., Rand R. P. Measured work of deformation and repulsion of lecithin bilayers. Proc Natl Acad Sci U S A. 1979 Jun;76(6):2750–2754. doi: 10.1073/pnas.76.6.2750. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Puskin J. S. Divalent cation binding to phospholipids: an EPR study. J Membr Biol. 1977 Jun 24;35(1):39–55. doi: 10.1007/BF01869939. [DOI] [PubMed] [Google Scholar]
- Rand R. P. Interacting phospholipid bilayers: measured forces and induced structural changes. Annu Rev Biophys Bioeng. 1981;10:277–314. doi: 10.1146/annurev.bb.10.060181.001425. [DOI] [PubMed] [Google Scholar]
- Rand R. P., Kachar B., Reese T. S. Dynamic morphology of calcium-induced interactions between phosphatidylserine vesicles. Biophys J. 1985 Apr;47(4):483–489. doi: 10.1016/S0006-3495(85)83941-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rand R. P., Parsegian V. A. Mimicry and mechanism in phospholipid models of membrane fusion. Annu Rev Physiol. 1986;48:201–212. doi: 10.1146/annurev.ph.48.030186.001221. [DOI] [PubMed] [Google Scholar]
- Rand R. P., Parsegian V. A. Physical force considerations in model and biological membranes. Can J Biochem Cell Biol. 1984 Aug;62(8):752–759. doi: 10.1139/o84-097. [DOI] [PubMed] [Google Scholar]
- Rosenberg J., Düzgüneş N., Kayalar C. Comparison of two liposome fusion assays monitoring the intermixing of aqueous contents and of membrane components. Biochim Biophys Acta. 1983 Oct 26;735(1):173–180. doi: 10.1016/0005-2736(83)90272-9. [DOI] [PubMed] [Google Scholar]
- Segal J. Lanthanum increases the rat thymocyte cytoplasmic free calcium concentration by enhancing calcium influx. Biochim Biophys Acta. 1986 Apr 29;886(2):267–271. doi: 10.1016/0167-4889(86)90144-8. [DOI] [PubMed] [Google Scholar]
- Siegel D. P. Inverted micellar intermediates and the transitions between lamellar, cubic, and inverted hexagonal lipid phases. I. Mechanism of the L alpha----HII phase transitions. Biophys J. 1986 Jun;49(6):1155–1170. doi: 10.1016/S0006-3495(86)83744-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Siegel D. P. Inverted micellar intermediates and the transitions between lamellar, cubic, and inverted hexagonal lipid phases. II. Implications for membrane-membrane interactions and membrane fusion. Biophys J. 1986 Jun;49(6):1171–1183. doi: 10.1016/S0006-3495(86)83745-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smaal E. B., Nicolay K., Mandersloot J. G., de Gier J., de Kruijff B. 2H-NMR, 31P-NMR and DSC characterization of a novel lipid organization in calcium-dioleoylphosphatidate membranes. Implications for the mechanism of the phosphatidate calcium transmembrane shuttle. Biochim Biophys Acta. 1987 Mar 12;897(3):453–466. doi: 10.1016/0005-2736(87)90442-1. [DOI] [PubMed] [Google Scholar]
- Smith T. C. The effect of lanthanum on electrophoretic mobility and passive cation movements of the Ehrlich ascites tumor cell. J Cell Physiol. 1976 Jan;87(1):47–52. doi: 10.1002/jcp.1040870107. [DOI] [PubMed] [Google Scholar]
- Szoka F., Jr, Papahadjopoulos D. Procedure for preparation of liposomes with large internal aqueous space and high capture by reverse-phase evaporation. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4194–4198. doi: 10.1073/pnas.75.9.4194. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Takata M., Pickard W. F., Lettvin J. Y., Moore J. W. Ionic conductance changes in lobster axon membrane when lanthanum is substituted for calcium. J Gen Physiol. 1966 Nov;50(2):461–471. doi: 10.1085/jgp.50.2.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsui F. C., Ojcius D. M., Hubbell W. L. The intrinsic pKa values for phosphatidylserine and phosphatidylethanolamine in phosphatidylcholine host bilayers. Biophys J. 1986 Feb;49(2):459–468. doi: 10.1016/S0006-3495(86)83655-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Westman J., Eriksson L. E. The interaction of various lanthanide ions and some anions with phosphatidylcholine vesicle membranes. A 31P NMR study of the surface potential effects. Biochim Biophys Acta. 1979 Oct 19;557(1):62–78. doi: 10.1016/0005-2736(79)90090-7. [DOI] [PubMed] [Google Scholar]
- Wilschut J., Düzgüneş N., Fraley R., Papahadjopoulos D. Studies on the mechanism of membrane fusion: kinetics of calcium ion induced fusion of phosphatidylserine vesicles followed by a new assay for mixing of aqueous vesicle contents. Biochemistry. 1980 Dec 23;19(26):6011–6021. doi: 10.1021/bi00567a011. [DOI] [PubMed] [Google Scholar]
- Wilschut J., Düzgüneş N., Papahadjopoulos D. Calcium/magnesium specificity in membrane fusion: kinetics of aggregation and fusion of phosphatidylserine vesicles and the role of bilayer curvature. Biochemistry. 1981 May 26;20(11):3126–3133. doi: 10.1021/bi00514a022. [DOI] [PubMed] [Google Scholar]
- Wilschut J., Nir S., Scholma J., Hoekstra D. Kinetics of Ca2+-induced fusion of cardiolipin-phosphatidylcholine vesicles: correlation between vesicle aggregation, bilayer destabilization, and fusion. Biochemistry. 1985 Aug 13;24(17):4630–4636. doi: 10.1021/bi00338a023. [DOI] [PubMed] [Google Scholar]
- Wilschut J., Scholma J., Bental M., Hoekstra D., Nir S. Ca2+-induced fusion of phosphatidylserine vesicles: mass action kinetic analysis of membrane lipid mixing and aqueous contents mixing. Biochim Biophys Acta. 1985 Nov 21;821(1):45–55. doi: 10.1016/0005-2736(85)90151-8. [DOI] [PubMed] [Google Scholar]
- Winiski A. P., McLaughlin A. C., McDaniel R. V., Eisenberg M., McLaughlin S. An experimental test of the discreteness-of-charge effect in positive and negative lipid bilayers. Biochemistry. 1986 Dec 16;25(25):8206–8214. doi: 10.1021/bi00373a013. [DOI] [PubMed] [Google Scholar]
- van Breemen C., De Weer P. Lanthanum inhibition of 45Ca efflux from the squid giant axon. Nature. 1970 May 23;226(5247):760–761. doi: 10.1038/226760a0. [DOI] [PubMed] [Google Scholar]
- van Dijck P. W., de Kruijff B., Verkleij A. J., van Deenen L. L., de Gier J. Comparative studies on the effects of pH and Ca2+ on bilayers of various negatively charged phospholipids and their mixtures with phosphatidylcholine. Biochim Biophys Acta. 1978 Sep 11;512(1):84–96. doi: 10.1016/0005-2736(78)90219-5. [DOI] [PubMed] [Google Scholar]
