- PDB-7usy: Structure of C. elegans TMC-1 complex with ARRD-6 -
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基本情報
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データベース: PDB / ID: 7usy
タイトル
Structure of C. elegans TMC-1 complex with ARRD-6
要素
(Transmembrane ...) x 2
ARRestin Domain protein
CALMyrin (Calcium and Integrin Binding protein) homolog
キーワード
MEMBRANE PROTEIN / Complex
機能・相同性
機能・相同性情報
detection of stimulus involved in sensory perception / striated muscle dense body / sensory perception of chemical stimulus / mechanosensitive monoatomic ion channel activity / non-motile cilium / sodium channel activity / monoatomic ion channel activity / calcium ion homeostasis / protein transport / monoatomic ion transmembrane transport ...detection of stimulus involved in sensory perception / striated muscle dense body / sensory perception of chemical stimulus / mechanosensitive monoatomic ion channel activity / non-motile cilium / sodium channel activity / monoatomic ion channel activity / calcium ion homeostasis / protein transport / monoatomic ion transmembrane transport / neuronal cell body / calcium ion binding / magnesium ion binding / membrane / plasma membrane / cytoplasm 類似検索 - 分子機能
ジャーナル: Nature / 年: 2022 タイトル: Structures of the TMC-1 complex illuminate mechanosensory transduction. 著者: Hanbin Jeong / Sarah Clark / April Goehring / Sepehr Dehghani-Ghahnaviyeh / Ali Rasouli / Emad Tajkhorshid / Eric Gouaux / 要旨: The initial step in the sensory transduction pathway underpinning hearing and balance in mammals involves the conversion of force into the gating of a mechanosensory transduction channel. Despite the ...The initial step in the sensory transduction pathway underpinning hearing and balance in mammals involves the conversion of force into the gating of a mechanosensory transduction channel. Despite the profound socioeconomic impacts of hearing disorders and the fundamental biological significance of understanding mechanosensory transduction, the composition, structure and mechanism of the mechanosensory transduction complex have remained poorly characterized. Here we report the single-particle cryo-electron microscopy structure of the native transmembrane channel-like protein 1 (TMC-1) mechanosensory transduction complex isolated from Caenorhabditis elegans. The two-fold symmetric complex is composed of two copies each of the pore-forming TMC-1 subunit, the calcium-binding protein CALM-1 and the transmembrane inner ear protein TMIE. CALM-1 makes extensive contacts with the cytoplasmic face of the TMC-1 subunits, whereas the single-pass TMIE subunits reside on the periphery of the complex, poised like the handles of an accordion. A subset of complexes additionally includes a single arrestin-like protein, arrestin domain protein (ARRD-6), bound to a CALM-1 subunit. Single-particle reconstructions and molecular dynamics simulations show how the mechanosensory transduction complex deforms the membrane bilayer and suggest crucial roles for lipid-protein interactions in the mechanism by which mechanical force is transduced to ion channel gating.
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