The Journal of Membrane Biology

, Volume 44, Issue 2, pp 135–158 | Cite as

Reversible inhibition of anion exchange in human erythrocytes by an inorganic disulfonate, tetrathionate

  • B. Deuticke
  • M. v. Bentheim
  • E. Beyer
  • D. Kamp
Article

Summary

Tetrathionate (S4O 6 −− ) markedly inhibits anion exchange across the human erythrocyte membrane. This phenomenon has been studied in order to obtain further insight into the mechanism of action of reversible inhibitors, in particular disulfonate inhibitors, of anion exchange. Anion fluxes were measured by tracer techniques at equilibrium. The following results were obtained: Tetrathionate, although an inorganic compound, inhibits the self-exchange of sulfate and of divalent organic anions (oxalate, malonate) noncompetitively atK i values (≦0.5mm) as yet only observed for amphiphilic inhibitors. The inhibitor is effective only from the outside of the cell. The inhibition is temperature-dependent,K i increasing by a factor of 5 between 5 and 35°C, and instantaneously and fully reversible. The presence of small monovalent anions (fluoride, bromide, chloride, nitrate, acetate) counteracts inhibition by tetrathionate to a varying and concentration-dependent extent, divalent anions have only a minor effect at high concentrations. Chloride exchange is also inhibited, while glycolate and lactate fluxes are much less sensitive or almost insensitive, in agreement with their alleged transfer by a different transport system. Tetrathionate is unique in its inhibitory action, its structural congeners, peroxodisulfate (S2O 8 −− ) and ethanedisulfonate (C2H4S2O 6 −− ) are much less effective.

The results can be interpreted by assuming that tetrathionate inhibits the movement of anions via the inorganic anion exchange system by binding-in a 1∶1 stoichiometry-to inhibitory “modifier sites”, for which it competes with other anions. These sites are located only on the exofacial surface of the membrane. The high affinity of tetrathionate is probably due to a local excess of π electrons in the region of its central disulfide bond. These may stabilize the binding by their ability to form electron donor-acceptor complexes with membrane sites, thus compensating for the absence of a hydrophobic binding domain in tetrathionate.

Keywords

Human Erythrocyte Organic Anion Anion Exchange Anion Flux Modifier Site 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    Barzilay, M., Cabantchik, Z.I. 1978. DNDS: A high affinity reversible probe for anion transport sites in human RBC membranes.Biophys. J. 21:11a Google Scholar
  2. 2.
    Barzilay, M., Ship, S., Cabantchik Z.I. 1978. Structure-activity relationship of aromatic sulfonic acids as inhibitors of the anion transport system of human RBC.Biophys. J. 21:71a Google Scholar
  3. 3.
    Beutler, E., Duron, O., Kelly, B.M. 1963. Improved method for the determination of blood glutathione.J. Lab. Clin. Med. 61:882Google Scholar
  4. 4.
    Brahm, J. 1977. Temperature-dependent changes of chloride transport kinetics in human red cells.J. Gen. Physiol. 70:283Google Scholar
  5. 5.
    Brazy, P.C., Gunn, R.B. 1976. Furosemide inhibition of chloride transport in human red blood cells.J. Gen. Physiol. 68:583Google Scholar
  6. 6.
    Cabantchik, Z.I., Knauf, P.A., Rothstein, A. 1978. The anion transport system of the red blood cell: The role of membrane protein evaluated by the use of “probes”.Biochim. Biophys. Acta (in press) Google Scholar
  7. 7.
    Cabantchik, Z.I., Rothstein, A. 1972. The nature of the membrane sites controlling anion permeability of human red blood cells as determined by studies with disulfonic stilbene derivatives.J. Membrane Biol. 10:311Google Scholar
  8. 8.
    Cousin, J.L., Motais, R. 1975. The role of carbonic anhydrase inhibitors on anion permeability into ox red blood cells.J. Physiol. (London) 256:61Google Scholar
  9. 9.
    Cousin, J.L., Motais, R. 1978. Effect of phloretin on chloride permeability: A structure-activity study.Biochim. Biophys. Acta 507:531Google Scholar
  10. 10.
    Dalmark, M. 1975. Chloride transport in human red cells.J. Physiol. (London) 250:39Google Scholar
  11. 11.
    Dalmark, M. 1976. Effects of halides and bicarbonate on chloride transport in human red blood cells.J. Gen. Physiol. 67:223Google Scholar
  12. 12.
    Dalmark, M., Wieth, J.O. 1972. Temperature dependence of chloride, bromide, iodide, thiocyanate and salicylate transport in human red cells.J. Physiol. (London) 224:583Google Scholar
  13. 13.
    Deuticke, B. 1970. Anion permeability of the red blood cell. Naturwissenschaften57:172Google Scholar
  14. 14.
    Deuticke, B. 1977. Properties and structural basis of simple diffusion pathways in the erythrocyte membrane.Rev. Physiol. Biochem. Pharmacol. 78:1Google Scholar
  15. 15.
    Deuticke, B., Kim, M., Zöllner, Chr. 1973. The influence of amphotericin B on the permeability of mammalian erythrocytes to nonelectrolytes, anions and cations.Biochim. Biophys. Acta 318:345Google Scholar
  16. 16.
    Deuticke, B., Rickert, I., Beyer, E. 1978. Stereoselective, SH-dependent transfer of lactate in mammalian erythrocytes.Biochim. Biophys. Acta 507:137Google Scholar
  17. 17.
    Foss, O., Furberg, S., Zachariasen, H. 1954. The crystal structure of barium tetrathionate dihydrate.Acta Chem. Scand. 8:459Google Scholar
  18. 18.
    Gunn, R.B., Dalmark, M., Tosteson, D.C., Wieth, J.O. 1973. Characteristics of chloride transport in human red blood cells.J. Gen. Physiol. 61:185Google Scholar
  19. 19.
    Haest, C.W.M., Deuticke, B. 1976. Possible relationship between membrane proteins and phospholipid asymmetry in the human erythrocyte membrane.Biochim. Biophys. Acta 436:353Google Scholar
  20. 20.
    Haest, C.W.M., Kamp, D., Plasa, G., Deuticke, B. 1977. Intra- and intermolecular cross-linking of membrane proteins in intact erythrocytes and ghosts by SH-oxidizing agents.Biochim. Biophys. Acta 469:226Google Scholar
  21. 21.
    Haest, C.W.M., Plasa, G., Kamp, D., Deuticke, B. 1978. Spectrin as a stabilizer of the phospholipid asymmetry in the human erythrocyte membrane.Biochim. Biophys. Acta 509:21Google Scholar
  22. 22.
    Halestrap, A.P. 1976. Transport of pyruvate and lactate into human erythrocytes. Evidence for the involvement of the chloride carrier and a chloride-independent carrier.Biochem. J. 156:193Google Scholar
  23. 23.
    Hunter, M.J. 1977. Human erythrocyte anion permeabilities measured under conditions of net charge transfer.J. Physiol. (London) 268:35Google Scholar
  24. 24.
    Kaplan, J.H., Scorah, K., Fasold, H., Passow, H. 1976. Sidedness of the inhibitory action of disulfonic acids on chloride equilibrium exchange and net transport across the human erythrocyte membrane.FEBS Lett. 62:182Google Scholar
  25. 25.
    Knauf, P.A., McCulloch, L., Marchant, P., Ship, S., Rothstein, A. 1977. Reversible interactions of the photoaffinity probe, NAP-taurine, with the anion exchange system of the human erythrocyte.Proc. Int. Union Physiol. Sci. 13:392Google Scholar
  26. 26.
    Lassen, U.V., Pape, L., Vestergaard-Bogind, B. 1974. A possible value for the resistance of theamphiuma red cell membrane.In: Comparative Biochemistry and Physiology of Transport, L. Bolis, K. Bloch, S. E. Luria and F. Lynen, editors. p. 363. North Holland, Amsterdam-LondonGoogle Scholar
  27. 27.
    Lepke, S., Fasold, H., Pring, M. 1976. A study of the relationship between inhibition of anion exchange and binding to the red blood cell membrane of 4,4′-diisothiocyano stilbene-2,2′-disulfonic acid (DIDS) and its dihydro derivative (H2DIDS).J. Membrane Biol. 29:147Google Scholar
  28. 28.
    Lepke, S., Passow, H. 1973. Asymmetric inhibition by phlorizin of sulfate movements across the red blood cell membrane.Biochim. Biophys. Acta 298:529Google Scholar
  29. 29.
    Mootz, D., Wunderlich, H. 1970. Kristallstrukturen von Säure-hydraten und Oxoniumsalzen. IV. Dioxonium-äthan-1,2-disulfonat (H3O)2(O3SCH2CH2SO3).Acta Crystallogr. Sect. B 26:1820Google Scholar
  30. 30.
    Motais, R., Cousin, J.L. 1976. The inhibitor effect of probenecid and structural analogues on organic anions and chloride permeabilities in ox erythrocytes.Biochim. Biophys. Acta 419:309Google Scholar
  31. 31.
    Passow, H., Pring, M., Legrum-Schuhmann, B., Zaki, L. 1976. The action of 2-(4′-amino phenyl)-6-methyl benzene thiazol 3,7′-disulfonic acid (APMB) on anion transport and the protein in band 3 of the red blood cell membrane.In: FEBS Symposium on the Biochemistry of Membrane Transport. Springer-Verlag.Google Scholar
  32. 32.
    Rothstein, A., Cabantchik, Z.I., Knauf, P. 1976. Mechanism of anion transport in red blood cells: Role of membrane proteins.Fed. Proc. 35:3Google Scholar
  33. 33.
    Sachs, J.R., Knauf, P.A., Dunham, P.B. 1975. Transport through red cell membranes.In: The Red Blood Cell. (2nd Ed.) D.McN. Surgenor, editor. Vol. 2, p. 613. Academic Press, New York-San Francisco-LondonGoogle Scholar
  34. 34.
    Scatchard, G., Yap, W.T. 1964. The physical chemistry of protein solutions. XII. The effects of temperature and hydroxide ion on the binding of small anions to human serum albumin.J. Am. Chem. Soc. 86:3434Google Scholar
  35. 35.
    Schnell, K.F. 1972. On the mechanism of inhibition of the sulfate transfer across the human erythrocyte membrane.Biochim. Biophys. Acta 282:265Google Scholar
  36. 36.
    Schnell, K.F., Gerhardt, S., Lepke, S., Passow, H. 1973. Asymmetric inhibition by phlorizin of halide movements across the red blood cell membrane.Biochim. Biophys. Acta 318:474Google Scholar
  37. 37.
    Schnell, K.F., Gerhardt, S., Schöppe-Fredenburg, A. 1977. Kinetic characteristics of the sulfate self-exchange in human red blood cells and red blood cell ghosts.J. Membrane Biol. 30:319Google Scholar
  38. 38.
    Shami, Y., Rothstein, A., Knauf, Ph.A. 1978. Identification of the Cl transport site of human red blood cells by a kinetic analysis of the inhibitory effect of a chemical probe.Biochim. Biophys. Acta 508:357Google Scholar
  39. 39.
    Tosteson, D.C., Gunn, R.B., Wieth, J.O. 1973. Chloride and hydroxyl ion conductance of sheep red cell membrane.In: Erythrocytes, Thrombocytes, Leukocytes. E. Gerlach, K. Moser, E. Deutsch, and W. Wilmanns editors. p. 62. Thieme-Verlag, StuttgartGoogle Scholar
  40. 40.
    Wieth, J.O. 1970. Effect of some monovalent anions on chloride and sulphate permeability of human red cells.J. Physiol. (London) 207:581Google Scholar
  41. 41.
    Zachariasen, W.H., Mooney, R.C.L. 1934. The atomic arrangement in ammonium and caesium persulphate (NH4)2S2O8 and Cs2S2O8, and the structure of the persulphate group.Z. Kristallographie 88:63Google Scholar
  42. 42.
    Zaki, L., Fasold, H., Schuhmann, B., Passow, H. 1975. Chemical modification of membrane proteins in relation to inhibition of anion exchange in human red blood cells.J. Cell. Physiol. 86:471Google Scholar
  43. 43.
    Zaki, L., Ruffing, W., Gärtner, E.M., Fasold, H., Motais, R., Passow, H. 1977. Band 3 as site of action of reversibly binding inhibitors of anion transport across the red cell membrane. 11th FEBS Meeting Copenhagen, August 1977.Abstr. No. A4-17-671Google Scholar

Copyright information

© Springer-Verlag New York Inc. 1978

Authors and Affiliations

  • B. Deuticke
    • 1
  • M. v. Bentheim
    • 1
  • E. Beyer
    • 1
  • D. Kamp
    • 1
  1. 1.Department of Physiology, Medical FacultyTechnical University AachenAachenGermany

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