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Perturbation analysis of the voltage-sensitive conformational changes of the Na+/glucose cotransporter

机译:Na + /葡萄糖共转运蛋白的电压敏感构象变化的扰动分析

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Conformational changes of the human Na+/glucose cotransporter (hSGLT1) were studied using voltage-jump methods. The cotransporter was expressed in Xenopus laevis oocytes, and SGLT1 charge movements were measured in the micro- to millisecond time scale using the cut-open oocyte preparation and in the millisecond to second time scale using the two-electrode voltage clamp method. Simultaneous charge and fluorescence changes were studied using tetramethylrhodamine-6-maleimide-labeled hSGLT1 Q457C. In 100 mM external [Na+], depolarizing voltage steps evoked a charge movement that rose initially to a peak (with time constant tau = 0.17 ms) before decaying to steady state with two time constants (tau = 2-30 and 25-150 ms). The time to peak (0.9 ms) decreased with [Na+], and was not observed in 0 mM [Na+]. In absence of Na+, charge movement decayed monotonically to steady state with three time constants (0.2, 2, and 150 ms). Charge movement was accompanied by fluorescence changes with similar time courses, indicating that global conformational changes monitored by charge movement are reflected by local environmental changes at or near Q457C. Our results indicate that the major voltage-dependent step of the Na+/glucose transport cycle is the return of the empty carrier from inward to outward facing conformations. Finally, we observed subtle differences between time constants for charge movement and for optical changes, suggesting that optical recordings can be used to monitor local conformational changes that underlie the global conformational changes of cotransporters.
机译:使用电压跳跃方法研究了人类Na + /葡萄糖共转运蛋白(hSGLT1)的构象变化。该共转运蛋白在非洲爪蟾卵母细胞中表达,并使用开孔卵母细胞制备物在微秒至毫秒的时间尺度内以及在双电极电压钳制方法下在毫秒至秒的时间尺度内测量SGLT1电荷运动。使用四甲基罗丹明-6-马来酰亚胺标记的hSGLT1 Q457C研究了电荷和荧光的同时变化。在100 mM外部[Na +]中,去极化电压阶跃引起电荷运动,该运动最初上升至峰值(时间常数tau = 0.17 ms),然后衰减至具有两个时间常数(tau = 2-30和25-150 ms的稳态) )。峰时间(0.9 ms)随着[Na +]的减少而降低,而在0 mM [Na +]中则未观察到。在没有Na +的情况下,电荷运动以三个时间常数(0.2、2和150 ms)单调衰减至稳态。电荷移动伴随着具有类似时程的荧光变化,这表明由电荷移动监控的整体构象变化反映在Q457C或附近的局部环境变化。我们的结果表明,Na + /葡萄糖转运周期的主要电压依赖性步骤是空载体从向内构型返回到面向外构型。最后,我们观察到了电荷移动和光学变化的时间常数之间的细微差异,这表明光学记录可用于监测作为共转运蛋白整体构象变化基础的局部构象变化。

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