Department of Pharmacology, Northwestern University, Feinberg School of Medicine, Chicago, IL.
Molecular Medicine, Hospital for Sick Children, Toronto, Canada.
J Gen Physiol. 2020 Jan 6;152(1). doi: 10.1085/jgp.201912397.
Store-operated Orai1 channels regulate a wide range of cellular functions from gene expression to cell proliferation. Previous studies have shown that gating of Orai1 channels is regulated by the outer pore residues V102 and F99, which together function as a hydrophobic gate to block ion conduction in resting channels. Opening of this gate occurs through a conformational change that moves F99 away from the permeation pathway, leading to pore hydration and ion conduction. In addition to this outer hydrophobic gate, several studies have postulated the presence of an inner gate formed by the basic residues R91, K87, and R83 in the inner pore. These positively charged residues were suggested to block ion conduction in closed channels via mechanisms involving either electrostatic repulsion or steric occlusion by a bound anion plug. However, in contrast to this model, here we find that neutralization of the basic residues dose-dependently abolishes both STIM1-mediated and STIM1-independent activation of Orai1 channels. Molecular dynamics simulations show that loss of the basic residues dehydrates the pore around the hydrophobic gate and stabilizes the pore in a closed configuration. Likewise, the severe combined immunodeficiency mutation, Orai1 R91W, closes the channel by dewetting the hydrophobic stretch of the pore and stabilizing F99 in a pore-facing configuration. Loss of STIM1-gating in R91W and in the other basic residue mutants is rescued by a V102A mutation, which restores pore hydration at the hydrophobic gate to repermit ion conduction. These results indicate that the inner pore basic residues facilitate opening of the principal outer hydrophobic gate through a long-range effect involving hydration of the outer pore.
储存操纵的 Orai1 通道调节从基因表达到细胞增殖等广泛的细胞功能。先前的研究表明,Orai1 通道的门控由外孔残基 V102 和 F99 调节,它们共同作为一个疏水性门,在静止通道中阻止离子传导。该门的打开通过构象变化发生,该变化使 F99 远离渗透途径,导致孔水合和离子传导。除了这个外疏水性门之外,几项研究还假设存在由内孔中的碱性残基 R91、K87 和 R83 形成的内门。这些带正电荷的残基通过涉及静电排斥或通过结合的阴离子塞的空间阻碍的机制被建议在封闭通道中阻止离子传导。然而,与该模型相反,我们在这里发现,碱性残基的中和剂量依赖性地消除了 STIM1 介导的和 STIM1 非依赖性的 Orai1 通道的激活。分子动力学模拟表明,碱性残基的丢失使疏水门周围的孔脱水,并使孔稳定在关闭构象。同样,严重联合免疫缺陷突变体 Orai1 R91W 通过使疏水孔段脱水并使 F99 稳定在面向孔的构象来关闭通道。在 R91W 和其他碱性残基突变体中失去 STIM1 门控通过 V102A 突变得到挽救,该突变使疏水门处的孔水合恢复,从而重新允许离子传导。这些结果表明,内孔碱性残基通过涉及外孔水合的远程效应促进主要外疏水性门的打开。