Abstract
Thin lipid (optically black) membranes were made from sheep red cell lipids dissolved in n-decane. The flux of Br across these membranes was measured by the use of tracer 82Br. The unidirectional flux of Br (in 50–100 mM NaBr) was 1–3 x 10-12 mole/cm2sec. This flux is more than 1000 times the flux predicted from the membrane electrical resistance (>108 ohm-cm2) and the transference number for Br- (0.2–0.3), which was estimated from measurements of the zero current potential difference. The Br flux was not affected by changes in the potential difference imposed across the membrane (±60 mv) or by the ionic strength of the bathing solutions. However, the addition of a reducing agent, sodium thiosulfate (10-3 M), to the NaBr solution bathing the membrane caused a 90% reduction in the Br flux. The inhibiting effect of S2O3 = suggests that the Br flux is due chiefly to traces of Br2 in NaBr solutions. As expected, the addition of Br2 to the NaBr solutions greatly stimulated the Br flux. However, at constant Br2 concentration, the Br flux was also stimulated by increasing the Br- concentration, in spite of the fact that the membrane was virtually impermeable to Br-. Finally, the Br flux appeared to saturate at high Br2 concentrations, and the saturation value was roughly proportional to the Br- concentration. These results can be explained by a model which assumes that Br crosses the membrane only as Br2 but that rapid equilibration of Br between Br2 and Br- occurs in the unstirred layers of aqueous solution bathing the two sides of the membrane. A consequence of the model is that Br- "facilitates" the diffusion of Br across the unstirred layers.
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Selected References
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- Andreoli T. E., Bangham J. A., Tosteson D. C. The formation and properties of thin lipid membranes from HK and LK sheep red cell lipids. J Gen Physiol. 1967 Jul;50(6):1729–1749. doi: 10.1085/jgp.50.6.1729. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Andreoli T. E., Dennis V. W., Weigl A. M. The effect of amphotericin B on the water and nonelectrolyte permeability of thin lipid membranes. J Gen Physiol. 1969 Feb;53(2):133–156. doi: 10.1085/jgp.53.2.133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bangham A. D., Standish M. M., Watkins J. C. Diffusion of univalent ions across the lamellae of swollen phospholipids. J Mol Biol. 1965 Aug;13(1):238–252. doi: 10.1016/s0022-2836(65)80093-6. [DOI] [PubMed] [Google Scholar]
- Dalmark M., Wieth J. O. Chloride and sodium permeabilities of human red cells. Biochim Biophys Acta. 1970 Dec 1;219(2):525–527. doi: 10.1016/0005-2736(70)90239-7. [DOI] [PubMed] [Google Scholar]
- Gutknecht J., Tosteson D. C. Ionic peremability of thin lipid membranes. Effects of n-alkyl alcohols, polyvalent cations, and a secondary amine. J Gen Physiol. 1970 Mar;55(3):359–374. doi: 10.1085/jgp.55.3.359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Harris E. J., Pressman B. C. Obligate cation exchanges in red cells. Nature. 1967 Dec 2;216(5118):918–920. doi: 10.1038/216918a0. [DOI] [PubMed] [Google Scholar]
- Henn F. A., Thompson T. E. Synthetic lipid bilayer membranes. Annu Rev Biochem. 1969;38:241–262. doi: 10.1146/annurev.bi.38.070169.001325. [DOI] [PubMed] [Google Scholar]
- Holz R., Finkelstein A. The water and nonelectrolyte permeability induced in thin lipid membranes by the polyene antibiotics nystatin and amphotericin B. J Gen Physiol. 1970 Jul;56(1):125–145. doi: 10.1085/jgp.56.1.125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hunter F. R. Facilitated diffusion in the chloride shift in human erythrocytes. Biochim Biophys Acta. 1967 Sep 9;135(4):784–787. doi: 10.1016/0005-2736(67)90109-5. [DOI] [PubMed] [Google Scholar]
- Pagano R., Thompson T. E. Spherical lipid bilayer membranes: electrical and isotopic studies of ion permeability. J Mol Biol. 1968 Nov 28;38(1):41–57. doi: 10.1016/0022-2836(68)90127-7. [DOI] [PubMed] [Google Scholar]
- Papahadjopoulos D., Watkins J. C. Phospholipid model membranes. II. Permeability properties of hydrated liquid crystals. Biochim Biophys Acta. 1967 Sep 9;135(4):639–652. doi: 10.1016/0005-2736(67)90095-8. [DOI] [PubMed] [Google Scholar]
- Rothfield L., Finkelstein A. Membrane biochemistry. Annu Rev Biochem. 1968;37:463–496. doi: 10.1146/annurev.bi.37.070168.002335. [DOI] [PubMed] [Google Scholar]
- Scarpa A., Cecchetto A., Azzone G. F. The mechanism of anion translocation and pH equilibration in erythrocytes. Biochim Biophys Acta. 1970;219(1):179–188. doi: 10.1016/0005-2736(70)90073-8. [DOI] [PubMed] [Google Scholar]
- Tosteson D. C. Electrolyte composition and transport in red blood cells. Fed Proc. 1967 Nov-Dec;26(6):1805–1812. [PubMed] [Google Scholar]