Literature DB >> 479826

Asymmetry in the mechanism for anion exchange in human red blood cell membranes. Evidence for reciprocating sites that react with one transported anion at a time.

R B Gunn, O Fröhlich.   

Abstract

The kinetics of chloride and bromide transport were examined in intact human red blood cells and resealed ghosts. Because the influx and efflux of halide ions are almost equal (less than 0.01% difference), the stimulation of the exchange flux by external halides could be determined by measuring 36Cl or 82Br efflux. When the external halide concentration was increased by replacement of isoionic, isotonic solutions of sucrose and the nontransported anion citrate, the stimulation of the exchange flux was hyperbolic and was maximum at 20 mM halide externally. The K 1/2-out, the external concentration of chloride or bromide which stimulated the efflux to half of its maximum value, was 3 and 1 mM respectively, 15-fold smaller than K 1/2-in which we found to be about equal to the K 1/2 of halide self-exchange with nearly equal internal and external concentrations. Thus, the transport mechanism behaves asymmetrically with respect to these transported halides. Bromide flux was two-fold greater in bromide-chloride heteroexchange than in bromide-bromide self-exchange but it was still much smaller than the chloride self-exchange flux. The maximum influx and efflux of bromide in exchange for chloride were roughly eqal. Thus, since the maximum transport rates in the two directions are nearly equal, the kinetics of bromide equilibrium exchange with equal concentrations on the two sides are controlled on the inside where K 1/2 is greatest. The K 1/2-out Cl was a hyperbolic function of internal chloride concentration and was proportional to the maximum flux at each internal chloride concentration. These results are evaluated in terms of two broad categories of models. We conclude that, in contrast to other ion transport systems which have been shown to have kinetics of a sequential mechanism, anion exchange is compatible with a ping-pong mechanism in which a single site reciprocates between inside- and outside-facing orientations with asymmetric K 1/2 values.

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Year:  1979        PMID: 479826      PMCID: PMC2228524          DOI: 10.1085/jgp.74.3.351

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  57 in total

1.  The noncompetitive inhibitor WW781 senses changes in erythrocyte anion exchanger (AE1) transport site conformation and substrate binding.

Authors:  P A Knauf; N M Raha; L J Spinelli
Journal:  J Gen Physiol       Date:  2000-02       Impact factor: 4.086

2.  Evidence for a second binding/transport site for chloride in erythrocyte anion transporter AE1 modified at glutamate 681.

Authors:  Michael L Jennings
Journal:  Biophys J       Date:  2005-01-14       Impact factor: 4.033

3.  How Channel-Like is a Biological Carrier?: Studies with the Erythrocyte Anion Transporter.

Authors:  O Frohlich
Journal:  Biophys J       Date:  1984-01       Impact factor: 4.033

4.  Transport of H2S and HS(-) across the human red blood cell membrane: rapid H2S diffusion and AE1-mediated Cl(-)/HS(-) exchange.

Authors:  Michael L Jennings
Journal:  Am J Physiol Cell Physiol       Date:  2013-07-17       Impact factor: 4.249

5.  Electrodiffusion, barrier, and gating analysis of DIDS-insensitive chloride conductance in human red blood cells treated with valinomycin or gramicidin.

Authors:  J C Freedman; T S Novak
Journal:  J Gen Physiol       Date:  1997-02       Impact factor: 4.086

6.  Charges, currents, and potentials in ionic channels of one conformation.

Authors:  D Chen; R Eisenberg
Journal:  Biophys J       Date:  1993-05       Impact factor: 4.033

7.  Flux, coupling, and selectivity in ionic channels of one conformation.

Authors:  D P Chen; R S Eisenberg
Journal:  Biophys J       Date:  1993-08       Impact factor: 4.033

8.  Simple model can explain self-inhibition of red cell anion exchange.

Authors:  C Tanford
Journal:  Biophys J       Date:  1985-01       Impact factor: 4.033

9.  Apical membrane Cl-butyrate exchange: mechanism of short chain fatty acid stimulation of active chloride absorption in rat distal colon.

Authors:  V M Rajendran; H J Binder
Journal:  J Membr Biol       Date:  1994-07       Impact factor: 1.843

10.  Substrate-dependent reversal of anion transport site orientation in the human red blood cell anion-exchange protein, AE1.

Authors:  Philip A Knauf; Foon-Yee Law; Tze-Wah Vivian Leung; Austin U Gehret; Martha L Perez
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-29       Impact factor: 11.205

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