Bindels R J, van den Broek L A, van Os C H
Biochim Biophys Acta. 1987 Feb 12;897(1):83-92. doi: 10.1016/0005-2736(87)90317-8.
The kinetics of Na+-dependent phosphate uptake in rat renal brush-border membrane vesicles were studied under zero-trans conditions at 37 degrees C and the effect of pH on the kinetic parameters was determined. When the pH was lowered it turned out to be increasingly difficult to estimate initial rates of phosphate uptake due to an increase in aspecific binding of phosphate to the brush border membrane. When EDTA or beta-glycerophosphate was added to the uptake medium this aspecific binding was markedly reduced. At pH 6.8, initial rates of phosphate uptake were measured between 0.01 and 3.0 mM phosphate in the presence of 100 mM Na+. Kinetic analysis resulted in a non-linear Eadie-Hofstee plot, compatible with two modes of transport: one major low-affinity system (Km approximately equal to 1.3 mM), high-capacity system (Vmax approximately equal to 1.1 nmol/s per mg protein) and one minor high-affinity (Km approximately equal to 0.03 mM), low-capacity system (Vmax approximately equal to 0.04 nmol/s per mg protein). Na+-dependent phosphate uptake studied far from initial rate conditions i.e. at 15 s, frequently observed in the literature, led to a dramatic decrease in the Vmax of the low-affinity system. When both the extra- and intravesicular pH were increased from 6.2 to 8.5, the Km value of the low-affinity system increased, but when divalent phosphate is considered to be the sole substrate for the low-affinity system then the Km value is no longer pH dependent. In contrast, the Km value of the high-affinity system was not influenced by pH but the Vmax decreased dramatically when the pH is lowered from 8.5 to 6.2. These results suggest that the low-affinity, high-capacity system transports divalent divalent phosphate only while the high-affinity, low-capacity system may transport univalent as well as divalent phosphate. Raising medium sodium concentration from 100 to 250 mM increased Na+-dependent phosphate uptake significantly but the pH dependence of the phosphate transport was not influenced. This observation makes it rather unlikely that pH changes only affect the Na+ site of the Na+-dependent phosphate transport system.
在37℃的零转运条件下,研究了大鼠肾刷状缘膜囊泡中钠依赖性磷酸盐摄取的动力学,并测定了pH对动力学参数的影响。当pH降低时,由于磷酸盐与刷状缘膜的非特异性结合增加,估计磷酸盐摄取的初始速率变得越来越困难。当向摄取培养基中添加乙二胺四乙酸(EDTA)或β-甘油磷酸时,这种非特异性结合明显减少。在pH 6.8时,在100 mM Na+存在下,在0.01至3.0 mM磷酸盐之间测量磷酸盐摄取的初始速率。动力学分析产生了一个非线性的伊迪-霍夫斯泰(Eadie-Hofstee)图,与两种转运模式相符:一种主要的低亲和力系统(Km约等于1.3 mM),高容量系统(Vmax约等于1.1 nmol/s每毫克蛋白质)和一种次要的高亲和力(Km约等于0.03 mM),低容量系统(Vmax约等于0.04 nmol/s每毫克蛋白质)。在远离初始速率条件下(即15秒时)研究的钠依赖性磷酸盐摄取,这在文献中经常观察到,导致低亲和力系统的Vmax急剧下降。当囊泡外和囊泡内的pH从6.2增加到8.5时,低亲和力系统的Km值增加,但当二价磷酸盐被认为是低亲和力系统的唯一底物时,Km值不再依赖于pH。相反,高亲和力系统的Km值不受pH影响,但当pH从8.5降至6.2时,Vmax急剧下降。这些结果表明,低亲和力、高容量系统仅转运二价磷酸盐,而高亲和力、低容量系统可能转运一价和二价磷酸盐。将培养基钠浓度从100 mM提高到250 mM显著增加了钠依赖性磷酸盐摄取,但磷酸盐转运的pH依赖性不受影响。这一观察结果使得pH变化仅影响钠依赖性磷酸盐转运系统的钠位点的可能性相当小。