Mengual R, Claude-Schlageter M H, Poiree J C, Yagello M, Sudaka P
Laboratoire de Biochimie, Faculté de Médecine, Nice, France.
J Membr Biol. 1989 Jun;108(3):197-205. doi: 10.1007/BF01871734.
The experiments reported in this paper aim at characterizing the carboxylic acid transport, the interactions of pyruvate and citrate with their transport sites and specificity. The study of these carriers was performed using isotopic solutes for the influx measurements in brush-border membrane vesicles under zero trans conditions where the membrane potential was abolished with KCl preloading with valinomycin or equilibrium exchange conditions and delta psi = 0. Under zero trans condition and delta psi = 0, the influence of pyruvate concentrations on its initial rates of transport revealed the existence of two families of pyruvate transport sites, one with a high affinity for pyruvate (Kt = 88 microM) and a low affinity for sodium (Kt = 57.7 mM) (site I), the second one with a low affinity for pyruvate (Kt = 6.1 mM) and a high affinity for sodium (Kt = 23.9 mM) (site II). The coupling factor [Na]/[pyruvate] stoichiometry were determined at 0.25 mM and 8 mM pyruvate and estimated at 1.8 for site I, and 3 when the first and the second sites transport simultaneously. Under chemical equilibrium (delta psi congruent to 0) single isotopic labeling, transport kinetics of pyruvate carrier systems have shown a double interaction of pyruvate with the transporter; the sodium/pyruvate stoichiometry also expressed according to a Hill plot representation was n = 1.7. The direct method of measuring Na+/pyruvate stoichiometry from double labeling kinetics and isotopic exchange, for a time course, gives a n = 1.67. Studies of transport specificity, indicate that the absence of inhibition of lactate transport by citrate and the existence of competitive inhibition of lactate and citrate transports by pyruvate leads to the conclusion that the low pyruvate affinity site can be attributed to the citrate carrier (tricarboxylate) and the high pyruvate affinity site to the lactate carrier (monocarboxylate).
本文所报道的实验旨在表征羧酸转运、丙酮酸和柠檬酸与其转运位点的相互作用及特异性。这些载体的研究是通过使用同位素溶质在零转运条件下测量刷状缘膜囊泡中的流入量来进行的,其中膜电位通过用缬氨霉素预加载氯化钾或平衡交换条件而被消除,且Δψ = 0。在零转运条件和Δψ = 0下,丙酮酸浓度对其初始转运速率的影响揭示了存在两类丙酮酸转运位点,一类对丙酮酸具有高亲和力(Kt = 88 μM)且对钠具有低亲和力(Kt = 57.7 mM)(位点I),另一类对丙酮酸具有低亲和力(Kt = 6.1 mM)且对钠具有高亲和力(Kt = 23.9 mM)(位点II)。耦合因子[Na]/[丙酮酸]化学计量比在丙酮酸浓度为0.25 mM和8 mM时测定,位点I估计为1.8,当第一和第二位点同时转运时估计为3。在化学平衡(Δψ ≈ 0)单同位素标记下,丙酮酸载体系统的转运动力学显示丙酮酸与转运体存在双重相互作用;根据希尔图表示法表示的钠/丙酮酸化学计量比为n = 1.7。从双标记动力学和同位素交换直接测量Na⁺/丙酮酸化学计量比的方法,在一个时间过程中得出n = 1.67。转运特异性研究表明,柠檬酸对乳酸转运无抑制作用,而丙酮酸对乳酸和柠檬酸转运存在竞争性抑制,这导致得出结论:丙酮酸低亲和力位点可归因于柠檬酸载体(三羧酸),而丙酮酸高亲和力位点可归因于乳酸载体(单羧酸)。