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-Structure paper
タイトル | Molecular insights into the gating mechanisms of voltage-gated calcium channel Ca2.3. |
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ジャーナル・号・ページ | Nat Commun, Vol. 14, Issue 1, Page 516, Year 2023 |
掲載日 | 2023年1月31日 |
著者 | Yiwei Gao / Shuai Xu / Xiaoli Cui / Hao Xu / Yunlong Qiu / Yiqing Wei / Yanli Dong / Boling Zhu / Chao Peng / Shiqi Liu / Xuejun Cai Zhang / Jianyuan Sun / Zhuo Huang / Yan Zhao / |
PubMed 要旨 | High-voltage-activated R-type Ca2.3 channel plays pivotal roles in many physiological activities and is implicated in epilepsy, convulsions, and other neurodevelopmental impairments. Here, we ...High-voltage-activated R-type Ca2.3 channel plays pivotal roles in many physiological activities and is implicated in epilepsy, convulsions, and other neurodevelopmental impairments. Here, we determine the high-resolution cryo-electron microscopy (cryo-EM) structure of human Ca2.3 in complex with the α2δ1 and β1 subunits. The VSD is stabilized in the resting state. Electrophysiological experiments elucidate that the VSD is not required for channel activation, whereas the other VSDs are essential for channel opening. The intracellular gate is blocked by the W-helix. A pre-W-helix adjacent to the W-helix can significantly regulate closed-state inactivation (CSI) by modulating the association and dissociation of the W-helix with the gate. Electrostatic interactions formed between the negatively charged domain on S6, which is exclusively conserved in the Ca2 family, and nearby regions at the alpha-interacting domain (AID) and S4-S5 helix are identified. Further functional analyses indicate that these interactions are critical for the open-state inactivation (OSI) of Ca2 channels. |
リンク | Nat Commun / PubMed:36720859 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 3.1 Å |
構造データ | EMDB-33285, PDB-7xlq: |
化合物 | ChemComp-Y01: ChemComp-R16: ChemComp-3PE: ChemComp-CA: ChemComp-NAG: |
由来 |
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キーワード | MEMBRANE PROTEIN (膜タンパク質) / Voltage-gated calcium channel (電位依存性カルシウムチャネル) / CaV2.3 / Complex |