Are acidic lipid domains induced by extrinsic protein binding to membranes?

References

• Bazzi M. D., Nelsestuen G. L. Highly sequential binding of protein kinase C and related proteins to membranes. Biochemistry 1991; 30: 7961–7969
   PubMed Web of Science ®Google Scholar
• Bevers E. M., Confurius P., Zwaal R. F. A. Changes in membrane phospholipid distribution during platelet activation. Biochimica et Biophysica Acta 1983; 597: 57–66
   Google Scholar
• Birrell G. B., Griffith O. H. Cytochrome c induces phase separation in diphosphatidylglycerol-phosphatidycholine suspensions. Biochemistry 1976; 15: 2925–2929
   PubMed Web of Science ®Google Scholar
• Bloom J. W., Nesheim M. E., Mann K. G. Phospholipid binding properties of bovine factor V and factor Va. Biochemistry 1979; 18: 4419–4425
   PubMedGoogle Scholar
• Bode A. P., Sandberg H., Dombrose F. A., Lentz B. R. Association of factor V activity with membranous vesicles released from human platelets: requirement for platelet stimulation. Thrombosis Research 1985; 39: 49–61
   PubMedGoogle Scholar
• Cutsforth G. A., Whitaker R. N., Hermans J., Lentz B. R. A new model to describe extrinsic protein binding to phospholipid membranes of varying composition: application to human prothrombin and factor X. Biochemistry 1989; 28: 7453–7459
   PubMedGoogle Scholar
• Cutsforth G. A., Koppaka V., Krishnaswamy S., Wu J. R., Mann K. G., Lentz B. R. Analysis of bovine factor Va binding to acidic-lipid containing synthetic membrane: a simple thermodynamic model. Biochemistry 1994, submitted
   Google Scholar
• Dombose F. A., Gitel S. N., Zawalich K., Jackson C. M. The association of bovine prothrombin fragment 1 with phospholipid. Journal of Biological Chemistry 1979; 254: 5027–5040
   PubMedGoogle Scholar
• Hartmann W., Galla H.-J., Sackmann E. Binding of polylysine to charged bilayer membranes: molecular organization of a lipid-peptide complex. FEBS Letters 1977; 78: 169–172
   PubMed Web of Science ®Google Scholar
• Jones M. E., Lentz M. E., Dombrose F. A. Comparison of the abilities of synthetic and platelet-derived membranes to enhance thrombin formation. Thrombosis Research 1985; 39: 711–724
   PubMedGoogle Scholar
• Jones M. E., Lentz B. R. Phospholipid lateral organization in synthetic membranes as monitored by pyrene-labeled phospholipid: effects of temperature and prothrombin fragment 1 binding. Biochemistry 1986; 25: 567–574
   PubMedGoogle Scholar
• Lentz B. R., Hermans J. A new model to describe extrinsic protein binding to phospholipid membrane of varying composition: quantitative treatment. Biochemistry 1989; 28: 7459–7461
   Google Scholar
• Lentz B. R., Alford D. R., Jones M. E., Dombrose F. A. Calcium-dependent and independent interactions of prothrombin fragment 1 with phosphatidylglycerol/phosphatidylcholine unilamellar vesicles. Biochemistry 1985; 24: 6997–7005
   PubMedGoogle Scholar
• Lentz B. R., Wu J. R., Sorentino A. M., Carleton J. N. membrane binding induces lipid-specific changes in the denaturation profile of bovine prothrombin. Biophysical Journal 1991; 60: 942–951
   PubMedGoogle Scholar
• Lim T. K., Bloomfield V. A., Nelsestuen G. L. Structure of the prothrombin- and blood clotting factor X-membrane complexes. Biochemistry 1977; 16: 4177–4181
   PubMed Web of Science ®Google Scholar
• Mann K. G. The assembly of blood clotting complexes on membranes. Trends in Biochemical Sciences 1987; 12: 229–233
   Web of Science ®Google Scholar
• Mayer L. D., Nelsestuen G. L. Calcium-and prothrombin-induced lateral phase separation in membranes. Biochemistry 1981; 20: 2457–2463
   PubMedGoogle Scholar
• Mayer L. D., Nelsestuen G. L. Membrane lateral phase separation induced by proteins of the prothrombinase complex. Biochimica et Biophysica Acta 1983; 734: 48–53
   Google Scholar
• Nelsestuen G. L. Interaction of vitamin-K-dependent proteins with calcium ions and phospholipid membranes. Federation Proceedings 1978; 37: 2621–2625
   PubMedGoogle Scholar
• Papahadjopoulos D., Hanahan D. J. Observations on the interaction of phospholipids and certain clotting factors. Biochimica Biophysica Acta 1964; 90: 436–439
   PubMed Web of Science ®Google Scholar
• Pei G., Powers D. D., Lentz B. R. Specific contribution of different phospholipid surfaces to the activation of prothrombin by the fully assembled prothrombinase. Journal of Biological Chemistry 1993; 268: 3226–3233
   PubMedGoogle Scholar
• Pusey M. L, Mayer L. D., Wei G. J., Bloomfield V. A., Nelsestuen G. L. Kinetics of hydrodynamic analysis of blood clotting factor V-membrane binding. Biochemistry 1982; 21: 5262–5269
   PubMedGoogle 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. Thrombosis Research 1985; 39: 63–79
   PubMed Web of Science ®Google Scholar
• Rietveld A., Berkhout T. A., Roenhorst A., Marsh D., de Kruiff B. Preferential association of apocytochrome c with negatively charged phospholipids in mixed model membranes. Biochimica et Biophysica Acta 1986; 858: 38–46
   PubMedGoogle Scholar
• Rosing J., Tans G., Speijer H., Zwaal R. F. A. Prothrombin activation on phospholipid membranes with positive electrostatic potential. Biochemistry 1988; 27: 9048–9055
   PubMedGoogle Scholar
• Tendian S. W., Lentz B. R. Evaluation of membrane phase behavior as a tool to detect extrinsic protein-induced domain formation: binding of prothrombin to phosphatidylserine/ phosphatidylcholine vesicles. Biochemistry 1990; 29: 6720–6729
   PubMedGoogle Scholar
• van Waart P., Bruls H, Hemker C., Lindhout T. Interaction of bovine blood clotting factor Va and its subunits with phospholipid vesicles. Biochemistry 1983; 22: 2427–2432
   PubMedGoogle Scholar
• Wei G. J., Bloomfield V. A., Resnick R. M., Nelsestuen G. L. Kinetic and mechanistic analysis of prothrombin-membrane binding by stopped flow light scattering. Biochemistry 1982; 21: 1949–1959
   PubMedGoogle Scholar
• Wiener J. R., Pal R., Barenholz Y., Wagner R. R. Influence of the peripheral matrix protein of vesicular stomatitis virus on the membrane dynamics of mixed phospholipid vesicles: fluorescence studies. Biochemistry 1985; 24: 7651–7658
   PubMedGoogle Scholar
• Wu J. R., Lentz B. R. Fourier transform infrared spectroscopic study of Ca2+ and membrane-induced secondary structural changes in bovine prothrombin and prothrombin fragment 1. Biophysical Journal 1991; 60: 70–80
   PubMedGoogle Scholar