Verkman A S, Ives H E
Biochemistry. 1986 May 20;25(10):2876-82. doi: 10.1021/bi00358a021.
The pH, delta pH, and membrane potential dependences of H+/OH-permeability in renal brush border membrane vesicles (BBMV) were studied by using the entrapped pH indicator 6-carboxyfluorescein (6CF). Quantitative H+/OH-fluxes (JH) were obtained from a calibration of the fluorescence response of 6CF to intravesicular pH using vesicles prepared with varying intravesicular and solution pHs. Intravesicular buffer capacity, determined by titration of lysed vesicles, increased monotonically from 140 to 260 mequiv/L in the pH range 5-8. JH was measured by subjecting voltage-clamped BBMV (K+/valinomycin) to preformed pH gradients over the pH range 5-8 and measuring the rate of change of intravesicular pH. For small preformed pH gradients (0.4 pH unit) JH [6 nequiv s-1 (mg of protein)-1] was nearly independent of pH (5-8), predicting a highly pH dependent H+ permeability coefficient. JH increased in a curvilinear manner from 6 to 104 nequiv s-1 (mg of protein)-1 as delta pH increased from 0.4 to 2.5. JH increased linearly [1.6-7.3 nequiv s-1 (mg of protein)-1] with induced K+ diffusion potentials (21-83 mV) in the absence of a pH gradient. These findings cannot be explained by simple diffusion of H+ or OH- or by mobile carrier models. Two mechanisms are proposed, including a lipid diffusion mechanism, facilitated by binding of H+/OH- to fixed sites in the membrane, and a linear H2O strand model, where dissociation of H2O in the membrane fixes H+ and OH- concentrations in strands, which can result in net H+/OH- transport.
利用包封的pH指示剂6-羧基荧光素(6CF)研究了肾刷状缘膜囊泡(BBMV)中H⁺/OH⁻通透性对pH、ΔpH和膜电位的依赖性。通过使用不同囊内pH和溶液pH制备的囊泡,根据6CF对囊内pH的荧光响应校准,获得了定量的H⁺/OH⁻通量(JH)。通过对裂解囊泡进行滴定测定的囊内缓冲容量,在pH范围5 - 8内从140单调增加到260 mequiv/L。通过使电压钳制的BBMV(K⁺/缬氨霉素)在pH范围5 - 8上经受预先形成的pH梯度,并测量囊内pH的变化速率来测量JH。对于小的预先形成的pH梯度(0.4个pH单位),JH [6 nequiv s⁻¹(mg蛋白质)⁻¹]几乎与pH(5 - 8)无关,预测H⁺通透性系数高度依赖于pH。随着ΔpH从0.4增加到2.5,JH以曲线方式从6增加到104 nequiv s⁻¹(mg蛋白质)⁻¹。在没有pH梯度的情况下,JH随着诱导的K⁺扩散电位(21 - 83 mV)呈线性增加[1.6 - 7.3 nequiv s⁻¹(mg蛋白质)⁻¹]。这些发现不能用H⁺或OH⁻的简单扩散或移动载体模型来解释。提出了两种机制,包括一种脂质扩散机制,由H⁺/OH⁻与膜中固定位点的结合促进,以及一种线性H₂O链模型,其中膜中H₂O的解离固定了链中的H⁺和OH⁻浓度,这可导致净H⁺/OH⁻转运。