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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1 April 1972
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April 01 1972
The Permeability of Thin Lipid Membranes to Bromide and Bromine
John Gutknecht,
John Gutknecht
From the Department of Physiology and Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
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L. J. Bruner,
L. J. Bruner
From the Department of Physiology and Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
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D. C. Tosteson
D. C. Tosteson
From the Department of Physiology and Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
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John Gutknecht
From the Department of Physiology and Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
L. J. Bruner
From the Department of Physiology and Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
D. C. Tosteson
From the Department of Physiology and Pharmacology, Duke University Medical Center, Durham, North Carolina 27710.
Dr. Bruner's present address is the Department of Physics, University of California, Riverside, California 92502.
Received:
August 25 1971
Online ISSN: 1540-7748
Print ISSN: 0022-1295
Copyright © 1972 by The Rockefeller University Press
1972
J Gen Physiol (1972) 59 (4): 486–502.
Article history
Received:
August 25 1971
Citation
John Gutknecht, L. J. Bruner, D. C. Tosteson; The Permeability of Thin Lipid Membranes to Bromide and Bromine . J Gen Physiol 1 April 1972; 59 (4): 486–502. doi: https://doi.org/10.1085/jgp.59.4.486
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