8IO0

Cryo-EM structure of human HCN3 channel with cAMP

8IO0 の概要

• エントリーDOI: 10.2210/pdb8io0/pdb
• EMDBエントリー: 35603
• 分子名称: Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3, ADENOSINE-3',5'-CYCLIC-MONOPHOSPHATE (2 entities in total)
• 機能のキーワード: human hcn3 channel, membrane protein
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 345888.51

構造登録者

Yu, B.,Lu, Q.Y.,Li, J.,Zhang, J. (登録日: 2023-03-10, 公開日: 2024-11-13, 最終更新日: 2025-06-25)

主引用文献

Yu, B.,Lu, Q.,Li, J.,Cheng, X.,Hu, H.,Li, Y.,Che, T.,Hua, Y.,Jiang, H.,Zhang, Y.,Xian, C.,Yang, T.,Fu, Y.,Chen, Y.,Nan, W.,McCormick, P.J.,Xiong, B.,Duan, J.,Zeng, B.,Li, Y.,Fu, Y.,Zhang, J.
Cryo-EM structure of human HCN3 channel and its regulation by cAMP.
J.Biol.Chem., 300:107288-107288, 2024

PubMed Abstract: HCN channels are important for regulating heart rhythm and nerve activity and have been studied as potential drug targets for treating depression, arrhythmia, nerve pain, and epilepsy. Despite possessing unique pharmacological properties, HCN channels share common characteristics in that they are activated by hyperpolarization and modulated by cAMP and other membrane lipids. However, the mechanisms of how these ligands bind and modulate HCN channels are unclear. In this study, we solved structures of full-length human HCN3 using cryo-EM and captured two different states, including a state without any ligand bound and a state with cAMP bound. Our structures reveal the novel binding sites for cholesteryl hemisuccinate in apo state and show how cholesteryl hemisuccinate and cAMP binding cause conformational changes in different states. These findings explain how these small modulators are sensed in mammals at the molecular level. The results of our study could help to design more potent and specific compounds to influence HCN channel activity and offer new therapeutic possibilities for diseases that lack effective treatment.

PubMed: 38636662
DOI: 10.1016/j.jbc.2024.107288

実験手法

ELECTRON MICROSCOPY (3.19 Å)