Loiseau A, Hill M, René-Corail L, Castaing M
U-426 INSERM, Paris, France.
Biochim Biophys Acta. 1995 Sep 13;1238(2):107-17. doi: 10.1016/0005-2736(95)00114-i.
The kinetics of the electroneutral exchange of competing sodium and potassium with protons across the membrane of large unilamellar vesicles (LUV) were determined at two pH values when transport was induced by the simultaneous presence of (222)C10-cryptand and FCCP (proton carrier) at various temperatures. The aim of the present work was to quantify the pH-dependent enthalpies of an ionizable mobile carrier affinities for competing alkali cations, and to focus on the effects of pH and temperature on the competitive transport selectivity of the carrier for K+ over Na+ ions. At any given temperature and pH, the apparent pH-dependent affinity of (222)C10 was higher for K+ than for Na+. The enthalpy of this affinity for K+ was significantly lower than that for Na+, whereas it varied similarly with the pH (delta H(KpHmK) = 32.8 and 37.0 kJ/mol, and delta H(KpHmNa) = 47.9 and 52.9 kJ/mol at pH 7.8 and 8.8, respectively). When using a kinetic model, the pH effect on these parameters was discriminated (delta H(KmK) = 37.9 kJ/mol and delta H(KmNa) = 53.9 kJ/mol). The pH-dependence of the delta H(KpHm) of the cations could therefore theoretically be shown to arise from the temperature-induced changes in the ionization of the buffer dissolved in the aqueous phases and of the amine groups of the binding cavity of the carrier. The K/Na competitive transport selectivity (Sc(K/Na)) of (222)C10 increased linearly with the K+ concentration. It decreased hyperbolically with increasing concentration of Na+ while being independent of pH at any given temperature. In equimolecular ionic mixtures, Sc(K/Na) varied from 2.2 to 3.0 when temperature rose from 20 degrees C to 35 degrees C (delta H(Sc(K/Na)) = 15.6 +/- 0.5 kJ/mol). The results are discussed in terms of the structural, physico-chemical and electrical characteristics of carriers and complexes.
当在不同温度下同时存在(222)C10 - 穴醚和FCCP(质子载体)诱导转运时,在两个pH值下测定了大单层囊泡(LUV)膜上竞争性钠、钾与质子的电中性交换动力学。本研究的目的是量化可电离移动载体对竞争性碱金属阳离子亲和力的pH依赖性焓,并关注pH和温度对载体对K⁺相对于Na⁺离子的竞争性转运选择性的影响。在任何给定温度和pH下,(222)C10对K⁺的表观pH依赖性亲和力高于对Na⁺的亲和力。这种对K⁺亲和力的焓显著低于对Na⁺的焓,而其随pH的变化情况类似(在pH 7.8和8.8时,ΔH(KpHmK)分别为32.8和37.0 kJ/mol,ΔH(KpHmNa)分别为47.9和52.9 kJ/mol)。使用动力学模型时,区分了pH对这些参数的影响(ΔH(KmK) = 37.9 kJ/mol,ΔH(KmNa) = 53.9 kJ/mol)。因此,理论上可以证明阳离子的ΔH(KpHm)的pH依赖性源于溶解在水相中的缓冲剂以及载体结合腔胺基团电离的温度诱导变化。(222)C10的K/Na竞争性转运选择性(Sc(K/Na))随K⁺浓度线性增加。随着Na⁺浓度增加,它呈双曲线下降,在任何给定温度下与pH无关。在等分子离子混合物中,当温度从20℃升至35℃时,Sc(K/Na)从2.2变化到3.0(ΔH(Sc(K/Na)) = 15.6 ± 0.5 kJ/mol)。根据载体和配合物的结构、物理化学和电学特性对结果进行了讨论。