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Identification of a proton sensor that regulates conductance and open time of single hERG channels

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Identification of a proton sensor that regulates conductance and open time of single hERG channels. / Wilson, Stacey L; Dempsey, Christopher E; Hancox, Jules C; Marrion, Neil V.

In: Scientific Reports, Vol. 9, 19825 (2019), 27.12.2019.

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@article{1a403783f8a74d7fa62bcc8b2f68c130,
title = "Identification of a proton sensor that regulates conductance and open time of single hERG channels",
abstract = "The hERG potassium channel influences ventricular action potential duration. Extracellular acidosis occurs in pathological states including cardiac ischaemia. It reduces the amplitude of hERG current and speeds up deactivation, which can alter cardiac excitability. This study aimed to identify the site of action by which extracellular protons regulate the amplitude of macroscopic hERG current. Recordings of macroscopic and single hERG1a and 1b channel activity, mutagenesis, and the recent cryoEM structure for hERG were employed. Single hERG1a and 1b channels displayed open times that decreased with membrane depolarization, suggestive of a blocking mechanism that senses approximately 20{\%} of the membrane electric field. This mechanism was sensitive to pH; extracellular acidosis reduced both hERG1a and1b channel open time and conductance. The effects of acidosis on macroscopic current amplitude and deactivation displayed different sensitivities to protons. Point mutation of a pair of residues (E575/H578) in the pore turret abolished the acidosis-induced decrease of current amplitude, without affecting the change in current deactivation. In single hERG1a channel recordings, the conductance of the double-mutant channel was unaffected by extracellular acidosis. These findings identify residues in the outer turret of the hERG channel that act as a proton sensor to regulate open time and channel conductance.",
keywords = "acidosis, hERG, ischaemia, pH, protons, proton sensor",
author = "Wilson, {Stacey L} and Dempsey, {Christopher E} and Hancox, {Jules C} and Marrion, {Neil V}",
year = "2019",
month = "12",
day = "27",
doi = "10.1038/s41598-019-56081-y",
language = "English",
volume = "9",
journal = "Scientific Reports",
issn = "2045-2322",
publisher = "Springer Nature",

}

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TY - JOUR

T1 - Identification of a proton sensor that regulates conductance and open time of single hERG channels

AU - Wilson, Stacey L

AU - Dempsey, Christopher E

AU - Hancox, Jules C

AU - Marrion, Neil V

PY - 2019/12/27

Y1 - 2019/12/27

N2 - The hERG potassium channel influences ventricular action potential duration. Extracellular acidosis occurs in pathological states including cardiac ischaemia. It reduces the amplitude of hERG current and speeds up deactivation, which can alter cardiac excitability. This study aimed to identify the site of action by which extracellular protons regulate the amplitude of macroscopic hERG current. Recordings of macroscopic and single hERG1a and 1b channel activity, mutagenesis, and the recent cryoEM structure for hERG were employed. Single hERG1a and 1b channels displayed open times that decreased with membrane depolarization, suggestive of a blocking mechanism that senses approximately 20% of the membrane electric field. This mechanism was sensitive to pH; extracellular acidosis reduced both hERG1a and1b channel open time and conductance. The effects of acidosis on macroscopic current amplitude and deactivation displayed different sensitivities to protons. Point mutation of a pair of residues (E575/H578) in the pore turret abolished the acidosis-induced decrease of current amplitude, without affecting the change in current deactivation. In single hERG1a channel recordings, the conductance of the double-mutant channel was unaffected by extracellular acidosis. These findings identify residues in the outer turret of the hERG channel that act as a proton sensor to regulate open time and channel conductance.

AB - The hERG potassium channel influences ventricular action potential duration. Extracellular acidosis occurs in pathological states including cardiac ischaemia. It reduces the amplitude of hERG current and speeds up deactivation, which can alter cardiac excitability. This study aimed to identify the site of action by which extracellular protons regulate the amplitude of macroscopic hERG current. Recordings of macroscopic and single hERG1a and 1b channel activity, mutagenesis, and the recent cryoEM structure for hERG were employed. Single hERG1a and 1b channels displayed open times that decreased with membrane depolarization, suggestive of a blocking mechanism that senses approximately 20% of the membrane electric field. This mechanism was sensitive to pH; extracellular acidosis reduced both hERG1a and1b channel open time and conductance. The effects of acidosis on macroscopic current amplitude and deactivation displayed different sensitivities to protons. Point mutation of a pair of residues (E575/H578) in the pore turret abolished the acidosis-induced decrease of current amplitude, without affecting the change in current deactivation. In single hERG1a channel recordings, the conductance of the double-mutant channel was unaffected by extracellular acidosis. These findings identify residues in the outer turret of the hERG channel that act as a proton sensor to regulate open time and channel conductance.

KW - acidosis

KW - hERG

KW - ischaemia

KW - pH

KW - protons

KW - proton sensor

UR - http://www.scopus.com/inward/record.url?scp=85077331835&partnerID=8YFLogxK

U2 - 10.1038/s41598-019-56081-y

DO - 10.1038/s41598-019-56081-y

M3 - Article

C2 - 31882846

AN - SCOPUS:85077331835

VL - 9

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 19825 (2019)

ER -