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Internal structure and visualization of transmembrane domains of the RyR1 calcium release channel by cryo‐EM

机译:RyR1钙释放通道跨膜结构域的内部结构和可视化

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摘要

RyR1 is an intracellular calcium channel with a central role in muscle contraction. We obtained a three‐dimensional reconstruction of the RyR1 in the closed state at a nominal resolution of ∼10 Å using cryo‐EM. The cytoplasmic assembly consists of a series of interconnected tubular structures that merge into four columns that extend into the transmembrane assembly. The transmembrane assembly, which has at least six transmembrane α‐helices per monomer, has four tilted rods that can be fitted with the inner helices of a closed K+ channel atomic structure. The rods splay out at the lumenal side and converge into a dense ring at the cytoplasmic side. Another set of four rods emerges from this ring and shapes the inner part of the four columns. The resulting constricted axial structure provides direct continuity between cytoplasmic and transmembrane assemblies, and a possible mechanism for control of channel gating through conformational changes in the cytoplasmic assembly.
机译:RyR1是细胞内钙通道,在肌肉收缩中起重要作用。我们使用cryo-EM获得了在闭合状态下RyR1的三维重构,标称分辨率约为10Å。胞质组件由一系列相互连接的管状结构组成,这些管状结构融合成四列,并延伸到跨膜组件中。跨膜组件,每个单体至少具有六个跨膜α螺旋,具有四个倾斜杆,可与封闭的K + 通道原子结构的内部螺旋配合。杆在管腔侧张开,并在细胞质侧汇聚成密集的环。另一组四根杆从该环中露出,并形成了四根圆柱的内部形状。产生的受约束的轴向结构提供了细胞质和跨膜组件之间的直接连续性,以及通过细胞质组件中构象变化控制通道门控的可能机制。

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