5va2 Citations

Cryo-EM Structure of the Open Human Ether-à-go-go-Related K+ Channel hERG.

Cell 169 422-430.e10 (2017)
Related entries: 5va1, 5va3

Cited: 270 times
EuropePMC logo PMID: 28431243

Abstract

The human ether-à-go-go-related potassium channel (hERG, Kv11.1) is a voltage-dependent channel known for its role in repolarizing the cardiac action potential. hERG alteration by mutation or pharmacological inhibition produces Long QT syndrome and the lethal cardiac arrhythmia torsade de pointes. We have determined the molecular structure of hERG to 3.8 Å using cryo-electron microscopy. In this structure, the voltage sensors adopt a depolarized conformation, and the pore is open. The central cavity has an atypically small central volume surrounded by four deep hydrophobic pockets, which may explain hERG's unusual sensitivity to many drugs. A subtle structural feature of the hERG selectivity filter might correlate with its fast inactivation rate, which is key to hERG's role in cardiac action potential repolarization.

Reviews - 5va2 mentioned but not cited (9)

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Articles - 5va2 mentioned but not cited (42)

  1. Cryo-EM Structure of the Open Human Ether-à-go-go-Related K+ Channel hERG. Wang W, MacKinnon R. Cell 169 422-430.e10 (2017)
  2. Gating mechanism of Kv11.1 (hERG) K+ channels without covalent connection between voltage sensor and pore domains. de la Peña P, Domínguez P, Barros F. Pflugers Arch 470 517-536 (2018)
  3. Determinants of Isoform-Specific Gating Kinetics of hERG1 Channel: Combined Experimental and Simulation Study. Perissinotti LL, De Biase PM, Guo J, Yang PC, Lee MC, Clancy CE, Duff HJ, Noskov SY. Front Physiol 9 207 (2018)
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  13. Allosteric Coupling Between Drug Binding and the Aromatic Cassette in the Pore Domain of the hERG1 Channel: Implications for a State-Dependent Blockade. Kudaibergenova M, Guo J, Khan HM, Zahid F, Lees-Miller J, Noskov SY, Duff HJ. Front Pharmacol 11 914 (2020)
  14. Revealing the efficacy-toxicity relationship of Fuzi in treating rheumatoid arthritis by systems pharmacology. Feng W, Liu J, Zhang D, Tan Y, Cheng H, Peng C. Sci Rep 11 23083 (2021)
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  16. Inhibition of the hERG potassium channel by phenanthrene: a polycyclic aromatic hydrocarbon pollutant. Al-Moubarak E, Shiels HA, Zhang Y, Du C, Hanington O, Harmer SC, Dempsey CE, Hancox JC. Cell Mol Life Sci 78 7899-7914 (2021)
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  39. research-article Harnessing AlphaFold to reveal state secrets: Prediction of hERG closed and inactivated states. Ngo K, Yarov-Yarovoy V, Clancy CE, Vorobyov I. bioRxiv 2024.01.27.577468 (2024)
  40. research-article Photo-crosslinking hERG channels causes a U.V.-driven, state-dependent disruption of kinetics and voltage dependence of activation. Codding SJ, Trudeau MC. bioRxiv 2024.01.09.574834 (2024)
  41. Structural modeling of hERG channel-drug interactions using Rosetta. Emigh Cortez AM, DeMarco KR, Furutani K, Bekker S, Sack JT, Wulff H, Clancy CE, Vorobyov I, Yarov-Yarovoy V. Front Pharmacol 14 1244166 (2023)
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