Friedel U, Wolbring G, Wohlfart P, Cook N J
Max-Planck-Institut für Biophysik, Abteilung für Molekulare Membranbiologie, Frankfurt am Main, F.R.G.
Biochim Biophys Acta. 1991 Jan 30;1061(2):247-52. doi: 10.1016/0005-2736(91)90290-o.
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+.
在将纯化的蛋白重组到蛋白脂质体中后,使用Ca2+敏感染料偶氮胂III研究了视杆光感受器钠钙交换体对K+的依赖性。发现Na+负载的脂质体对Ca2+的摄取在外部K+(EC50约为1 mM)存在时以米氏动力学方式大大增强,这表明一个K+离子参与一个Ca2+离子的转运。我们还发现在完全没有K+的情况下Ca2+摄取程度最低。其他碱金属阳离子,特别是Rb+,以及程度稍小的Cs+,也能够刺激Na+-Ca2+交换。我们还通过确定电化学K+梯度对蛋白脂质体中Na+激活的Ca2+外流的影响,研究了光感受器Na+-Ca2+交换体对K+的依赖性。我们发现,在使用FCCP进行膜电压钳制的条件下,内向的电化学K+梯度(即K0+大于Ki+)会抑制,而外向的电化学K+梯度(即Ki+大于K0+)会增强Na+依赖性Ca2+外流,这与K+与Ca2+同向共转运的观点一致。在生理(即Ki+ = 110 mM,K0+ = 2.5 mM)钾浓度下对重组交换体的研究表明,Ca2+外流对Na+的依赖性具有高度协同性(希尔图得出n = 3.01),这表明至少三个,但可能是四个,Na+离子与一个Ca2+离子进行交换。在这些条件下,重组交换体对Na+的Km为26.1 mM,每个交换体分子的周转数为115 Ca2+.s-1。因此,我们对视杆光感受器纯化和重组的钠钙交换体的研究结果与先前的报道(Cervetto, L., Lagnado, L., Perry, R.J., Robinson, D.W.和McNaughton, P.A.(1989年)《自然》337, 740 - 743;Schnetkamp, P.P.M., Basu, D.K.和Szerencsei, R.T.(1989年)《美国生理学杂志》257, C153 - C157)一致,即视杆光感受器的钠钙交换体在生理条件下以4 Na+:l Ca2+, 1K+的化学计量比共转运K+。