Department of Cellular and Molecular Physiology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033.
Beijing Key Laboratory of Gene Resources and Molecular Development College of Life Sciences, Beijing Normal University, Beijing 100875, China.
J Biol Chem. 2018 Aug 17;293(33):12962-12974. doi: 10.1074/jbc.RA118.003424. Epub 2018 Jun 28.
Store-operated Ca entry signals are mediated by plasma membrane Orai channels activated through intermembrane coupling with Ca-sensing STIM proteins in the endoplasmic reticulum (ER). The nature of this elaborate Orai-gating mechanism has remained enigmatic. Based on the Orai structure, mammalian Orai1 channels are hexamers comprising three dimeric subunit pairs. We utilized concatenated Orai1 dimers to probe the function of key domains within the channel pore and gating regions. The Orai1-E106Q selectivity-filter mutant, widely considered a dominant pore blocker, was surprisingly nondominant within concatenated heterodimers with Orai1-WT. The Orai1-E106Q/WT heterodimer formed STIM1-activated nonselective cation channels with significantly enlarged apparent pore diameter. Other Glu-106 substitutions entirely blocked the function of heterodimers with Orai1-WT. The hydrophobic pore-lining mutation V102C, which constitutively opens channels, was suppressed by Orai1-WT in the heterodimer. In contrast, the naturally occurring R91W pore-lining mutation associated with human immunodeficiency was completely dominant-negative over Orai-WT in heterodimers. Heterodimers containing the inhibitory K85E mutation extending outward from the pore helix gave an interesting partial effect on both channel activation and STIM1 binding, indicating an important allosteric link between the cytosolic Orai1 domains. The Orai1 C-terminal STIM1-binding domain mutation L273D powerfully blocked STIM1-induced channel activation. The Orai1-L273D/WT heterodimer had drastically impaired STIM1-induced channel gating but, unexpectedly, retained full STIM1 binding. This reveals the critical role of Leu-273 in transducing the STIM1-binding signal into the allosteric conformational change that initiates channel gating. Overall, our results provide important new insights into the role of key functional domains that mediate STIM1-induced gating of the Orai1 channel.
钙库操纵的钙内流信号由质膜 Orai 通道介导,该通道通过与内质网(ER)中钙感应 STIM 蛋白的膜间偶联而被激活。这种精细的 Orai 门控机制的性质仍然是个谜。基于 Orai 的结构,哺乳动物 Orai1 通道由包含三个二聚体亚基对的六聚体组成。我们利用串联的 Orai1 二聚体来探测通道孔和门控区域内关键结构域的功能。Orai1-E106Q 选择性滤器突变体,通常被认为是一种主要的通道阻断剂,在与 Orai1-WT 的串联异二聚体中出人意料地是非显性的。Orai1-E106Q/WT 异二聚体与 STIM1 激活的非选择性阳离子通道形成,其表观孔径明显增大。其他 Glu-106 取代物完全阻断了 Orai1-WT 异二聚体的功能。疏水的孔衬突变 V102C 构成性地打开通道,在异二聚体中被 Orai1-WT 抑制。相比之下,与人类免疫缺陷相关的天然发生的 R91W 孔衬突变在异二聚体中对 Orai-WT 完全是完全阴性的。从孔螺旋向外延伸的抑制性 K85E 突变包含的异二聚体对通道激活和 STIM1 结合都产生了有趣的部分效应,表明细胞溶质 Orai1 结构域之间存在重要的变构联系。Orai1 C 末端 STIM1 结合域突变 L273D 强力阻断 STIM1 诱导的通道激活。Orai1-L273D/WT 异二聚体 STIM1 诱导的通道门控严重受损,但出人意料的是,仍保留了完整的 STIM1 结合。这表明 Leu-273 在将 STIM1 结合信号转导为启动通道门控的变构构象变化中起着关键作用。总体而言,我们的研究结果为介导 STIM1 诱导的 Orai1 通道门控的关键功能结构域的作用提供了重要的新见解。