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Membrane surface charge dictates the structure and function of the epithelial Na+/H+ exchanger

机译:膜表面电荷决定上皮Na + / H +交换子的结构和功能

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摘要

The Na+/H+ exchanger NHE3 plays a central role in intravascular volume and acid–base homeostasis. Ion exchange activity is conferred by its transmembrane domain, while regulation of the rate of transport by a variety of stimuli is dependent on its cytosolic C-terminal region. Liposome- and cell-based assays employing synthetic or recombinant segments of the cytosolic tail demonstrated preferential association with anionic membranes, which was abrogated by perturbations that interfere with electrostatic interactions. Resonance energy transfer measurements indicated that segments of the C-terminal domain approach the bilayer. In intact cells, neutralization of basic residues in the cytosolic tail by mutagenesis or disruption of electrostatic interactions inhibited Na+/H+ exchange activity. An electrostatic switch model is proposed to account for multiple aspects of the regulation of NHE3 activity.
机译:Na + / H + 交换器NHE3在血管内体积和酸碱稳态中起着核心作用。离子交换活性由其跨膜结构域赋予,而各种刺激对转运速率的调节取决于其胞质C末端区域。基于脂质体和细胞的分析方法采用了胞质尾巴的合成或重组片段,证明了与阴离子膜的优先结合,而阴离子膜则被干扰静电相互作用的干扰所消除。共振能量转移测量表明,C末端区域的片段接近双层。在完整的细胞中,通过诱变或破坏静电相互作用中和胞浆尾巴中的碱性残基会抑制Na + / H + 交换活性。提出了静电开关模型来考虑NHE3活性调节的多个方面。

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