Boylan Center for Cellular and Molecular Physiology, Mount Desert Island Biological Laboratory, Salisbury Cove, Maine, USA.
Biophys J. 2012 Oct 17;103(8):1706-18. doi: 10.1016/j.bpj.2012.09.001. Epub 2012 Oct 16.
The signaling mechanisms that regulate CLC anion channels are poorly understood. Caenorhabditis elegans CLH-3b is a member of the CLC-1/2/Ka/Kb channel subfamily. CLH-3b is activated by meiotic cell-cycle progression and cell swelling. Inhibition is brought about by GCK-3 kinase-mediated phosphorylation of S742 and S747 located on a ∼176 amino acid disordered domain linking CBS1 and CBS2. Much of the inter-CBS linker is dispensable for channel regulation. However, deletion of a 14 amino acid activation domain encompassing S742 and S747 inhibits channel activity to the same extent as GCK-3. The crystal structure of CmCLC demonstrated that CBS2 interfaces extensively with an intracellular loop connecting membrane helices H and I, the C-terminus of helix D, and a short linker connecting helix R to CBS1. Point mutagenesis of this interface identified two highly conserved aromatic amino acid residues located in the H-I loop and the first α-helix (α1) of CBS2. Mutation of either residue to alanine rendered CLH-3b insensitive to GCK-3 inhibition. We suggest that the dephosphorylated activation domain normally interacts with CBS1 and/or CBS2, and that conformational information associated with this interaction is transduced through a conserved signal transduction module comprising the H-I loop and CBS2 α1.
调控 CLC 阴离子通道的信号机制还不太清楚。秀丽隐杆线虫 CLH-3b 是 CLC-1/2/Ka/Kb 通道亚家族的成员。CLH-3b 通过减数分裂细胞周期的进展和细胞肿胀而被激活。GCK-3 激酶介导的位于连接 CBS1 和 CBS2 的约 176 个氨基酸的无序域上的 S742 和 S747 的磷酸化导致其抑制。CBS1 和 CBS2 之间的大部分连接环对于通道调节是可有可无的。然而,缺失包含 S742 和 S747 的 14 个氨基酸激活域会使通道活性抑制到与 GCK-3 相同的程度。CmCLC 的晶体结构表明 CBS2 与连接膜螺旋 H 和 I、螺旋 D 的 C 末端以及连接螺旋 R 和 CBS1 的短链接的细胞内环广泛相互作用。该界面的点突变鉴定了位于 H-I 环和 CBS2 的第一个α螺旋(α1)中的两个高度保守的芳香族氨基酸残基。将任一残基突变为丙氨酸会使 CLH-3b 对 GCK-3 的抑制作用不敏感。我们认为,去磷酸化的激活域通常与 CBS1 和/或 CBS2 相互作用,并且与这种相互作用相关的构象信息通过包含 H-I 环和 CBS2 α1 的保守信号转导模块传递。