Literature DB >> 760792

The membrane valve: a consequence of asymmetrical inhibition of membrane carriers. I. Equilibrating transport systems.

R M Krupka, R Devés.   

Abstract

Facilitated membrane transport systems act as valves, or rectifiers, when the substrate affinities on the two sides of the membrane differ substantially, i.e. when the system is strongly asymmetric. The asymmetry may be intrinsic or imposed by a reversible competitive inhibitor acting on only one side of the membrane. Under non-equilibrium conditions such systems allow net movements of substrate to proceed faster, sometimes much faster, in one direction than the other, though the final equilibrium is unaffected. Obligatory exchange systems may also function as valves when inhibited unsymmetrically, permitting exchange to occur more rapidly with one distribution of substrates than with the reversed distribution. Here, unequal flux rates do not depend on unequal concentrations of the substrate on either side of the membrane, but may also occur with equal concentrations, provided the affinities of the two substrates differ. The kinetic theory leading to these conclusions is given here, and it is shown how individual parameters of a carrier system affect the efficiency, or tightness, of the valve. In addition, simple kinetic tests for the operation of a valve are outlined. Examples are cited of transport systems having inhibitor-binding sites on only one surface of the cell membrane, which could function normally as valves. Systems implicated are glucose transport in various cells, the ADP-ATP exchanger of mitochondria, the anion transporter of erythrocytes, and the Na+-K+ pump.

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Year:  1979        PMID: 760792     DOI: 10.1016/0005-2736(79)90116-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  6 in total

1.  Testing transport models and transport data by means of kinetic rejection criteria.

Authors:  R M Krupka
Journal:  Biochem J       Date:  1989-06-15       Impact factor: 3.857

Review 2.  Indicator dilution estimation of capillary endothelial transport.

Authors:  J B Bassingthwaighte; H V Sparks
Journal:  Annu Rev Physiol       Date:  1986       Impact factor: 19.318

3.  Asymmetrical binding of phloretin to the glucose transport system of human erythrocytes.

Authors:  R M Krupka
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

4.  Characteristics of lysine transport across the serosal pole of the anuran small intestine.

Authors:  C I Cheeseman
Journal:  J Physiol       Date:  1983-05       Impact factor: 5.182

5.  Effects of phorbol, dexamethasone and starvation on 3-O-methyl-D-glucose transport by rat thymocytes. Modulation of transport by altered trans effects.

Authors:  R J Naftalin; R J Rist
Journal:  Biochem J       Date:  1990-01-01       Impact factor: 3.857

6.  Amino acid inhibition and stimulation of 2-aminoisobutyric acid exit from anuran small intestine.

Authors:  C A Boyd; V S Perring
Journal:  J Physiol       Date:  1982-06       Impact factor: 5.182

  6 in total

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