scholarly journals Water permeability of gramicidin A-treated lipid bilayer membranes.

1978 ◽  
Vol 72 (3) ◽  
pp. 341-350 ◽  
Author(s):  
P A Rosenberg ◽  
A Finkelstein

In membranes containing aqueous pores (channels), the osmotic water permeability coefficient, P f, is greater than the diffusive water permeability coefficient, P d. In fact, the magnitude of P f/P d is commonly used to determine pore radius. Although, for membranes studied to date, P f/P d monotonically declines with decreasing pore radius, there is controversy over the value it theoretically assumes when that radius is so small that water molecules cannot overtake one another within the channel (single-file transport). In one view it should equal 1, and in another view it should equal N, the number of water molecules in the pore. Gramicidin A forms, in lipid bilayer membranes, narrow aqueous channels through which single-file transport may occur. For these channels we find that P f/P d approximately 5. In contrast, for the wider nystatin and amphotericin B pores, P f/P d approximately 3. These findings offer experimental support for the view that P f/P d = N for single-file transport, and we therefore conclude that there are approximately five water molecules in a gramicidin A channel. A similar conclusion was reached independently from streaming potential data. Using single-channel conductance data, we calculate the water permeability of an individual gramicidin A channel. In the Appendix we report that there is a wide range of channel sizes and lifetimes in cholesterol-containing membranes.

1978 ◽  
Vol 72 (3) ◽  
pp. 327-340 ◽  
Author(s):  
P A Rosenberg ◽  
A Finkelstein

For very narrow channels in which ions and water cannot overtake one another (single-file transport), electrokinetic measurements provide information about the number of water molecules within a channel. Gramicidin A is believed to form such narrow channels in lipid bilayer membranes. In 0.01 and 0.1 M solutions of CsCl, KCL, and NaCl, streaming potentials of 3.0 mV per osmolal osmotic pressure difference (created by urea, glycerol, or glucose) appear across gramicidin A-treated membranes. This implies that there are six to seven water molecules within a gramicidin channel. Electroosmotic experiments, in which the water flux assoicated with current flow across gramicidin-treated membranes is measured, corroborate this result. In 1 M salt solutions, streaming potentials are 2.35 mV per osmolal osmotic pressure difference instead of 3.0 mV. The smaller value may indicate multiple ion occupancy of the gramicidin channel at high salt concentrations. Apparent deviations from ideal cationic selectivity observed while attempting to measure single-salt dilution potentials across gramicidin-treated membranes result from streaming potential effects.


1976 ◽  
Vol 68 (2) ◽  
pp. 137-143 ◽  
Author(s):  
A Finkelstein

In artificial lipid bilayer membranes, the ratio of the water permeability coefficient (Pd(water)) to the permeability coefficient of an arbitrary nonelectrolyte such as n-butyramide (Pd(n-butyramide)) remains relatively constant with changes in lipid composition and temperature, even though the individual Pd's increase more than 100-fold. I propose that this is a general rule that also holds for the lipid bilayers of cells and tissues, and that therefore if Pd(water)/Pd(solute greatly exceeds the value found for artifical lipid bilayers (where "solute" is a molecule, such as 1,6 hexanediol or n-butyramide, that crosses the cell membrane by a solubility-diffusion mechanism without the aid of a special transporting system), then water crosses the cell membrane via aqueous pores. Applying this criterion to the toad urinary bladder, we find that even in the unstimulated bladder, water probably crosses the luminal membrane primarily through small aqueous pores, and that this almost certainly the case after antidiuretic hormone (ADH) stimulation. I suggest that ADH stimulation ultimately leads either to formation (or enlargement) of pores, by the rearrangement of preexisting subunits, or to an unplugging of these pores.


2018 ◽  
Vol 209 ◽  
pp. 9-33 ◽  
Author(s):  
Andreas Horner ◽  
Peter Pohl

After a short introduction into the single-file transport theory, we analyze experiments in which the unitary water permeability, pf, of water channel proteins (aquaporins, AQPs), potassium channels (KcsA), and antibiotics (gramicidin-A derivatives) has been obtained. A short outline of the underlying methods is also provided.


Author(s):  
Maciej Gliniak ◽  
Jakub Sikora ◽  
Urszula Sadowska ◽  
Agnieszka Klimek-Kopyra ◽  
Agnieszka Latawiec ◽  
...  

1982 ◽  
Vol 242 (4) ◽  
pp. F321-F330 ◽  
Author(s):  
E. Gonzalez ◽  
P. Carpi-Medina ◽  
G. Whittembury

Proximal straight tubules were dissected and mounted in a chamber with their lumina occluded. The well-stirred bath could be 95% changed within 84 ms to set up osmotic gradients (delta Coi) across the peritubular cell aspect. Volume changes (less than or equal to 10 pl/mm) were estimated from continuous records of diameter changes (error less than 0.1 micrometers). delta Coi greater than or equal to 2-3 mosM could be discerned. delta Coi values from 10 to 44 mosM were used to evaluate Posc, the cell osmotic water permeability coefficient, and extrapolated to delta Coi = 0. Posc = 25.1 (+/- 2.3) X 10(-4) cm3.s-1.osM-1.cm2 tubular surface area-1. These values are lower than those reported for Pose, the transepithelial osmotic water permeability coefficient, and become lower if corrected for the real (infolded) peritubular cell surface area. Thus, for a given osmotic difference, transcellular water flow finds a higher resistance than paracellular water flow. Experiments were also performed with delta Coi greater than 100 mosM, but interpretation of these data is difficult because of the presence of volume regulatory phenomena and other undesirable effects.


2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
Yurong Zhang ◽  
Shengxuan Xu ◽  
Zhaofeng Fang ◽  
Junzhi Zhang ◽  
Chaojun Mao

Water and gas permeability coefficients of concrete with different water-binder (w/b) ratios and admixtures were measured by a self-designed test device based on the steady-state flow method for liquid and the method of differential pressure in stability for gas, respectively. In addition, the micropore structure of concrete was determined by 1H nuclear magnetic resonance (NMR). Results indicated that there are good correlations between water and gas permeability of concrete with different w/b ratios, with correlation coefficient greater than 0.90. Better correlations between water permeability and segmental contributive porosity ranged from 10 to 100 nm and 100 to 1000 nm can be identified, but the gas permeability is more relevant to the segmental contributive porosity ranging from 100 to 1000 nm. Moreover, the correlation between water permeability and contributive porosity for each pore diameter is always better than that of gas permeability. The influence of admixtures on the relationship between permeability and pore size distribution of concrete is significant. Moreover, water permeability coefficient is one or two orders of magnitude lower than the gas permeability coefficient.


1989 ◽  
Vol 257 (5) ◽  
pp. C837-C850 ◽  
Author(s):  
A. S. Verkman

Water transport occurs in all biological membranes. A few selected membranes in the kidney, amphibian urinary bladder, and erythrocyte have very high water permeability and are thought to contain specialized water transporting units termed "water channels." The known biophysical properties of membranes containing water channels are a high osmotic water permeability coefficient (Pf), an osmotic-to-diffusional water permeability coefficient ratio (Pf/Pd) greater than unity, a low activation energy (Ea), and inhibition by mercurial compounds. The biochemical and molecular characteristics of water channel pathways are not known at present. Established and new methods to measure Pf and Pd in kidney tubules and in isolated membrane vesicles from kidney cells are reviewed and evaluated. In the mammalian proximal tubule, a high Pf results from transcellular movement of water across highly permeable apical and basolateral membranes containing water channels. It has been assumed that proximal tubule Pf is unregulated; however, recent results indicate that apical water channels are retrieved by endocytosis and that Pf is decreased fivefold with increasing transepithelial osmotic gradients. In the thin and thick ascending limbs, Pf is nearly the lowest of all biological membranes and is not subject to regulation. In contrast, collecting tubule Pf is subject to hormonal regulation by vasopressin. Vasopressin binding to receptors located at the basal membrane of principal cells initiates adenosine 3',5'-cyclic monophosphate production, which is thought ultimately to activate the exocytic insertion of intracellular vesicles containing water channels into the cell apical membrane. Vasopressin-induced endosomes from kidney collecting tubule and toad urinary bladder contain functional water channels but no proton pumps or urea transporters, supporting a membrane shuttle hypothesis that is selective for water channels. Future directions for the isolation and molecular cloning of kidney water channels are evaluated.


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