Burnham C, Munzesheimer C, Rabon E, Sachs G
Biochim Biophys Acta. 1982 Mar 8;685(3):260-72. doi: 10.1016/0005-2736(82)90066-9.
The absorbance change of the weak base dye probe, Acridine orange, was used to monitor alterations of pH gradients across renal brush border membrane vesicles. The presence of Na+/H+ or Li+/H+ exchange was demonstrated by diluting Na2SO4 or Li2SO4 loaded vesicles into Na+-or Li+-free solutions, which caused dye uptake. About 20% of the uptake was abolished by lipid permeable cations such as valinomycin-K+ or tetraphenylphosphonium, indicating perhaps the presence of a finite Na+ conductance smaller than electroneutral Na+/H+ exchange. The protonophore tetrachlorosalicylanilide raised the rate of dye uptake under these conditions, hence the presence of an Na+ conductance greater than the H+ conductance was suggested. K+ gradients also induced changes of pH, at about 10% of the Na+ or Li+ rate. Partial inhibition (21%) was seen with 0.1 mM amiloride indicating that K+ was a low affinity substrate for the Na+/H+ exchange. Acceleration both by tetrachlorosalicylanilide (2-fold) and valinomycin (4-fold) suggested the presence of 2 classes of vesicles, those with high and those with low K+ conductance. The larger magnitude of the valinomycin dependent signal suggested that 75% of the vesicles has a low K+ conductance. Inward Cl- gradients also induced acidification, partially inhibited by the presence of tetraphenylphosphonium, and accelerated by tetrachlorosalicylanilide. Thus both a Cl- conductance greater than the H+ conductance and a Cl-/OH- exchange were present. The rate of Na+/H+ exchange was amiloride sensitive with a pH optimum of 6.5 and an apparent Km for Na+ or Li+ of about 10 mM and an EA of 14.3 kcal per mol. A 61-fold Na2SO4 gradient resulted in a pH gradient of 1.64 units which increased to 1.8 with gramicidin. An equivalent NaCl gradient gave a much lower delta pH even in the presence of gramicidin showing that the H+ and Cl- pathways could alter the effect of the Na+/H+ exchange.
使用弱碱染料探针吖啶橙的吸光度变化来监测肾刷状缘膜囊泡跨膜pH梯度的变化。通过将负载Na2SO4或Li2SO4的囊泡稀释到无Na+或无Li+的溶液中证明了Na+/H+或Li+/H+交换的存在,这会导致染料摄取。脂质可渗透阳离子如缬氨霉素-K+或四苯基鏻可消除约20%的摄取,这可能表明存在有限的Na+电导率,其小于电中性Na+/H+交换。在这些条件下,质子载体四氯水杨酰苯胺提高了染料摄取速率,因此表明存在大于H+电导率的Na+电导率。K+梯度也会引起pH变化,其速率约为Na+或Li+速率的10%。0.1 mM氨氯吡咪可产生部分抑制作用(21%),表明K+是Na+/H+交换的低亲和力底物。四氯水杨酰苯胺(2倍)和缬氨霉素(4倍)均可加速反应,这表明存在两类囊泡,即具有高K+电导率和低K+电导率的囊泡。缬氨霉素依赖性信号的幅度更大,表明75%的囊泡具有低K+电导率。内向Cl-梯度也会引起酸化,四苯基鏻的存在可部分抑制该过程,而四氯水杨酰苯胺可加速该过程。因此,存在大于H+电导率的Cl-电导率和Cl-/OH-交换。Na+/H+交换速率对氨氯吡咪敏感,最适pH为6.5,Na+或Li+的表观Km约为10 mM,每摩尔的活化能为14.3 kcal。61倍的Na2SO4梯度导致pH梯度为1.64个单位,在短杆菌肽存在的情况下增加到1.8。即使在存在短杆菌肽的情况下,等效的NaCl梯度产生的ΔpH也低得多,这表明H+和Cl-途径可改变Na+/H+交换的效果。