Literature DB >> 1998696

The sodium-calcium exchanger of bovine rod photoreceptors: K(+)-dependence of the purified and reconstituted protein.

U Friedel1, G Wolbring, P Wohlfart, N J Cook.   

Abstract

The K(+)-dependence of the rod photoreceptor sodium-calcium exchanger was investigated using the Ca2(+)-sensitive dye arsenazo III after reconstitution of the purified protein into proteoliposomes. The uptake of Ca2+ by Na(+)-loaded liposomes was found to be greatly enhanced by the presence of external K+ (EC50 approximately 1 mM) in a Michaelis-Menten manner, suggesting that one K+ ion is involved in the transport of one Ca2+ ion. We also found a minimal degree of Ca2+ uptake in the total absence of K+. Other alkali cations, notably Rb+ and, to a lesser extent, Cs+, were also able to stimulate Na(+)-Ca2+ exchange. We also investigated the K(+)-dependence of the photoreceptor Na(+)-Ca2+ exchanger by determining the effects of electrochemical K+ gradients on the Na(+)-activated Ca2+ efflux from proteoliposomes. We found that, under conditions of membrane voltage clamp with FCCP, inwardly directed electrochemical K+ gradients (i.e., K0+ greater than Ki+) inhibited, whereas an outwardly directed electrochemical K+ gradient (i.e., Ki+ greater than K0+) enhanced, Na(+)-dependent Ca2+ efflux, consistent with the notion that K+ is cotransported in the same direction as Ca2+. The investigation of the reconstituted exchanger at physiological (i.e. Ki+ = 110 mM, K0+ = 2.5 mM) potassium concentrations revealed that the Na(+)-dependence of Ca2(+)-efflux was highly cooperative (n = 3.01 from Hill plots), indicating that at least three, but possibly four, Na+ ions are exchanged for one Ca2+ ion. Under these conditions the reconstituted exchanger showed a Km for Na+ of 26.1 mM, and a turnover number of 115 Ca2+.s-1 per exchanger molecule. Our results with the purified and reconstituted sodium-calcium exchanger from rod photoreceptors are therefore consistent with previous reports (Cervetto, L., Lagnado, L., Perry, R.J., Robinson, D.W. and McNaughton, P.A. (1989) Nature 337, 740-743; Schnetkamp, P.P.M., Basu, D.K. and Szerencsei, R.T. (1989) Am. J. Physiol. 257, C153-C157) that the sodium-calcium exchanger of rod photoreceptors cotransports K+ under physiological conditions with a stoichiometry of 4 Na+:1 Ca2+, 1K+.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1998696     DOI: 10.1016/0005-2736(91)90290-o

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


  5 in total

Review 1.  Signal transduction enzymes of vertebrate photoreceptors.

Authors:  J B Hurley
Journal:  J Bioenerg Biomembr       Date:  1992-04       Impact factor: 2.945

2.  Calcium-sensitive downregulation of the transduction chain in rod photoreceptors of the rat retina.

Authors:  Andreas Knopp; Hartmann Rüppel
Journal:  Biophys J       Date:  2006-05-12       Impact factor: 4.033

3.  Ca2+ fluxes and channel regulation in rods of the albino rat.

Authors:  A Knopp; H Rüppel
Journal:  J Gen Physiol       Date:  1996-05       Impact factor: 4.086

4.  The mechanism of ion transport by the Na(+)-Ca2+,K+ exchange in rods isolated from the salamander retina.

Authors:  R J Perry; P A McNaughton
Journal:  J Physiol       Date:  1993-07       Impact factor: 5.182

5.  Primary structure and functional expression of the Na/Ca,K-exchanger from bovine rod photoreceptors.

Authors:  H Reiländer; A Achilles; U Friedel; G Maul; F Lottspeich; N J Cook
Journal:  EMBO J       Date:  1992-05       Impact factor: 11.598

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.