Bacconi Andrea, Ravera Silvia, Virkki Leila V, Murer Heini, Forster Ian C
Institute of Physiology and Center for Integrative Human Physiology, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
J Membr Biol. 2007 Feb;215(2-3):81-92. doi: 10.1007/s00232-007-9008-1. Epub 2007 Apr 19.
The temperature dependence of the transport kinetics of flounder Na(+)-coupled inorganic phosphate (P(i)) cotransporters (NaPi-IIb) expressed in Xenopus oocytes was investigated using radiotracer and electrophysiological assays. (32)P(i) uptake was strongly temperature-dependent and decreased by approximately 80% at a temperature change from 25 degrees C to 5 degrees C. The corresponding activation energy (E (a)) was approximately 14 kcal mol(-1) for the cotransport mode. The temperature dependence of the cotransport and leak modes was determined from electrogenic responses to 1 mM P(i) and phosphonoformic acid (PFA), respectively, under voltage clamp. The magnitude of the P(i)- and PFA-induced changes in holding current decreased with temperature. E (a) at -100 mV for the cotransport and leak modes was approximately 16 kcal mol(-1) and approximately 11 kcal mol(-1), respectively, which suggested that the leak is mediated by a carrier, rather than a channel, mechanism. Moreover, E (a) for cotransport was voltage-independent, suggesting that a major conformational change in the transport cycle is electroneutral. To identify partial reactions that confer temperature dependence, we acquired presteady-state currents at different temperatures with 0 mM P(i) over a range of external Na(+). The relaxation time constants increased, and the peak time constant shifted toward more positive potentials with decreasing temperature. Likewise, there was a depolarizing shift of the charge distribution, whereas the total available charge and apparent valency predicted from single Boltzmann fits were temperature-independent. These effects were explained by an increased temperature sensitivity of the Na(+)-debinding rate compared with the other voltage-dependent rate constants.
利用放射性示踪和电生理分析方法,研究了非洲爪蟾卵母细胞中表达的比目鱼钠耦联无机磷酸盐(P(i))共转运体(NaPi-IIb)转运动力学的温度依赖性。(32)P(i)摄取强烈依赖于温度,在温度从25℃变为5℃时下降约80%。共转运模式的相应活化能(E(a))约为14 kcal mol(-1)。在电压钳制下,分别根据对1 mM P(i)和膦甲酸(PFA)的电生反应确定共转运和渗漏模式的温度依赖性。P(i)和PFA诱导的保持电流变化幅度随温度降低。共转运和渗漏模式在-100 mV时的E(a)分别约为16 kcal mol(-1)和约11 kcal mol(-1),这表明渗漏是由载体而非通道机制介导的。此外,共转运的E(a)与电压无关,表明转运循环中的主要构象变化是电中性的。为了确定赋予温度依赖性的部分反应,我们在一系列外部Na(+)浓度下,于不同温度下用0 mM P(i)获取了稳态前电流。随着温度降低,弛豫时间常数增加,峰值时间常数向更正的电位移动。同样,电荷分布出现去极化偏移,而单次玻尔兹曼拟合预测的总可用电荷和表观价态与温度无关。与其他电压依赖性速率常数相比,Na(+)解离速率的温度敏感性增加解释了这些效应。