+検索条件
-Structure paper
タイトル | Cryo-EM reveals two distinct serotonin-bound conformations of full-length 5-HT receptor. |
---|---|
ジャーナル・号・ページ | Nature, Vol. 563, Issue 7730, Page 270-274, Year 2018 |
掲載日 | 2018年10月31日 |
著者 | Sandip Basak / Yvonne Gicheru / Shanlin Rao / Mark S P Sansom / Sudha Chakrapani / |
PubMed 要旨 | The 5-HT serotonin receptor, a cationic pentameric ligand-gated ion channel (pLGIC), is the clinical target for management of nausea and vomiting associated with radiation and chemotherapies. Upon ...The 5-HT serotonin receptor, a cationic pentameric ligand-gated ion channel (pLGIC), is the clinical target for management of nausea and vomiting associated with radiation and chemotherapies. Upon binding, serotonin induces a global conformational change that encompasses the ligand-binding extracellular domain (ECD), the transmembrane domain (TMD) and the intracellular domain (ICD), the molecular details of which are unclear. Here we present two serotonin-bound structures of the full-length 5-HT receptor in distinct conformations at 3.32 Å and 3.89 Å resolution that reveal the mechanism underlying channel activation. In comparison to the apo 5-HT receptor, serotonin-bound states underwent a large twisting motion in the ECD and TMD, leading to the opening of a 165 Å permeation pathway. Notably, this motion results in the creation of lateral portals for ion permeation at the interface of the TMD and ICD. Combined with molecular dynamics simulations, these structures provide novel insights into conformational coupling across domains and functional modulation. |
リンク | Nature / PubMed:30401837 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 3.32 - 3.89 Å |
構造データ | |
化合物 | ChemComp-SRO: ChemComp-HOH: |
由来 |
|
キーワード | MEMBRANE PROTEIN |