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The kinetics of transport inhibition by noncompetitive inhibitors

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Summary

A new analysis of the conventional carrier model shows that noncompetitive inhibitors can give rise to either competitive, noncompetitive or uncompetitive kinetics; the true mechanism and also the relative affinity of the inhibitor on each surface of the membrane can be decided from the patterns of inhibition observed in different transport experiments. The priciples governing the kinetics of inhibition apply to both reversible and irreversible inhibitors, for in either case the substrate may increase or decrease inhibition or be without effect. Ambiguity arises if the noncompetitive inhibitor acts on only one side of the membrane and if the substrate, in the course of being transported, alters the steady-state distribution of the carrier between inner and outer forms. In facilitated transport systems only equilibrium exchange should give rise to noncompetitive kinetics, whatever the location of the inhibitor. In active systems even the interpretation of exchange in the final steadystate is complicated if the energy-coupling mechanism produces a large displacement in the distribution of the free carrier or the substrate complex: the inhibition could be competitive or uncompetitive, depending on the location of the inhibitor. The actual mechanism is revealed in the uncoupled system.

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References

  1. Basketter, D.A., Widdas, D.F. 1978. Asymmetry of the hexose transfer system in human erythrocytes. Comparison of the effects of cytochalasin B, phloretin and maltose as competitive inhibitors.J. Physiol. (London) 278:389–401

    CAS  Google Scholar 

  2. Devés, R., Krupka, R.M. 1978. A new approach in the kinetics of biological transport. The potential of reversible inhibition studies.Biochim. Biophys. Acta 510:186–200

    PubMed  Google Scholar 

  3. Devés, R., Krupka, R.M. 1978. Cytochalasin B and the kinetics of biological transport. A case of asymmetric binding to the glucose carrier.Biochim. Biophys. Acta 510:339–348

    PubMed  Google Scholar 

  4. Devés, R., Krupka, R.M. 1979. A general kinetic analysis of transport. Tests of the carrier model based on predicted relations among experimental parameters.Biochim. Biophys. Acta 556:533–547

    PubMed  Google Scholar 

  5. Devés, R., Krupka, R.M. 1981. Evidence for a twostate mobile carrier mechanism in erythrocyte choline transport: Effects of substrate analogs on inactivation of the carrier by N-ethylmaleimide.J. Membrane Biol. 61:21–30

    Article  Google Scholar 

  6. Devés, R., Krupka, R.M. 1981. Reaction of internal forms of the choline carrier of erythrocytes with N-ethylmaleimide: Evidence for a carrier conformational change on complex formation.J. Membrane Biol. 63:99–103

    Google Scholar 

  7. Edwards, P.A.W. 1973. Evidence for the carrier model of transport from the inhibition by N-ethylmaleimide of choline transport across the human red cell membrane.Biochim. Biophys. Acta 311:123–140

    CAS  PubMed  Google Scholar 

  8. Geck, P. 1971. Eigenschaften eines asymmetrischen Carrier-modells für den Zuckertransport am menschlichen Erythrozyten.Biochim. Biophys. Acta 241:462–472

    CAS  PubMed  Google Scholar 

  9. Hoare, D.G. 1972. The transport of L-leucine in human erythrocytes: A new kinetic analysis.J. Physiol. (London) 221:311–329

    CAS  Google Scholar 

  10. Krupka, R.M., Devés, R. 1980. The choline transport system of erythrocytes. Distribution of the free carrier in the membrane.Biochim. Biophys. Acta 600:228–232

    CAS  PubMed  Google Scholar 

  11. Levine, M., Oxender, D.L., Stein, W.D. 1965. The substrate-facilitated transport of the glucose-carrier across the human erythrocyte membrane.Biochim. Biophys. Acta 109:151–163

    CAS  PubMed  Google Scholar 

  12. Lieb, W.R., Stein, W.D. 1974. Testing and characterizing the simple carrier.Biochim. Biophys. Acta 373:178–196

    CAS  PubMed  Google Scholar 

  13. Lieb, W.R., Stein, W.D. 1976. Testing the simple carrier using irreversible inhibitors.Biochim. Biophys. Acta 455:913–927

    CAS  PubMed  Google Scholar 

  14. Martin, K. 1968. Concentrative accumulation of choline by human erythrocytes.J. Gen. Physiol. 51:497–516

    Article  CAS  PubMed  Google Scholar 

  15. Martin, K. 1971. Some properties of an SH group essential for choline transport in human erythrocytes.J. Physiol. (London) 213:647–667

    CAS  Google Scholar 

  16. Mawe, R.C., Hempling, H.G. 1965. The exchange of14C-glucose across the membrane of the human erythrocyte.J. Cell. Comp. Physiol. 66:95–103

    Article  CAS  Google Scholar 

  17. Miller, D.M. 1971. The kinetics of selective biological transport. V. Further data on the erythrocyte-monosaccharide transport system.Biophys. J. 11:915–923

    CAS  PubMed  Google Scholar 

  18. Regen, D.M., Morgan, H.E. 1964. Studies of the glucose transport system in the rabbit erythrocyte.Biochim. Biophys. Acta 79:151–166

    CAS  PubMed  Google Scholar 

  19. Regen, D.M., Tarpley, H.L. 1974. Anomalous transport kinetics and the glucose carrier hypothesis.Biochim. Biophys. Acta 339:218–233

    CAS  Google Scholar 

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Krupka, R.M. The kinetics of transport inhibition by noncompetitive inhibitors. J. Membrain Biol. 74, 175–182 (1983). https://doi.org/10.1007/BF02332121

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