Department of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, TN 37232.
Biochemistry. 2013 Nov 12;52(45):7964-74. doi: 10.1021/bi4012385. Epub 2013 Nov 1.
EmrD is the only structurally characterized drug/H(+) antiporter of the major facilitator superfamily (MFS). It has been crystallized in a doubly occluded conformation that is considered representative of an intermediate state in the transport cycle of MFS transporters. However, unexpected features of the crystal structure and the lack of functional information available for EmrD limit the utility of the structural data. To assess whether the crystal structure represents a stable state in a native-like environment, we used electron paramagnetic resonance (EPR) spectroscopy to determine the mobility and accessibility of spin labels at 76 positions in six transmembrane (TM) helices of EmrD reconstituted in liposomes. While the EPR data were mostly consistent with the crystal structure, they also revealed significant deviations from the predicted orientation and topology of TM helices at several locations. Additionally, we were unable to reproduce EmrD-dependent multidrug resistance phenotypes in vitro and in cell-based assays of drug transport. In spite of structural and functional discrepancies, we mapped a pH-dependent conformational change in which the cytoplasmic side of the N-terminal half opened locally in response to protonation. This conformational switch is consistent with the expected pH-dependent behavior of MFS H(+)-coupled antiporters.
EmrD 是主要易化子超家族 (MFS) 中唯一具有结构特征的药物/H(+)反向转运蛋白。它已被结晶为双重闭塞构象,被认为代表 MFS 转运蛋白运输循环中的中间状态。然而,晶体结构的意外特征和缺乏可用的 EmrD 功能信息限制了结构数据的实用性。为了评估晶体结构是否代表天然样环境中的稳定状态,我们使用电子顺磁共振 (EPR) 光谱来确定在脂质体中重建的 EmrD 的六个跨膜 (TM) 螺旋中的 76 个位置的自旋标记的迁移率和可及性。虽然 EPR 数据在大多数情况下与晶体结构一致,但它们也揭示了在几个位置 TM 螺旋的预测取向和拓扑结构存在显着偏差。此外,我们无法在体外和基于细胞的药物转运测定中重现 EmrD 依赖性多药耐药表型。尽管存在结构和功能上的差异,但我们绘制了 pH 依赖性构象变化的图谱,其中 N 端半部分的细胞质侧局部打开以响应质子化。这种构象转换与 MFS H(+) 偶联反向转运蛋白的预期 pH 依赖性行为一致。