Single channel properties of the slow cardiac potassium current, IKs

The slow potassium current, IKs, abbreviates the cardiac action potential by repolarizing the membrane to a resting state. Mutations in the pore-forming IKs subunit, KCNQ1, cause long QT syndrome type 1 (LQT1), which increases risk of fatal arrhythmia. Despite the physiological and clinical importa...

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Main Author: Werry, Daniel
Language:English
Published: University of British Columbia 2011
Online Access:http://hdl.handle.net/2429/38968
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spelling ndltd-UBC-oai-circle.library.ubc.ca-2429-389682018-01-05T17:25:30Z Single channel properties of the slow cardiac potassium current, IKs Werry, Daniel The slow potassium current, IKs, abbreviates the cardiac action potential by repolarizing the membrane to a resting state. Mutations in the pore-forming IKs subunit, KCNQ1, cause long QT syndrome type 1 (LQT1), which increases risk of fatal arrhythmia. Despite the physiological and clinical importance of IKs, little is known about the elementary events that underlie the unique biophysical properties of the channel, and how these elementary events are altered in the face of disease. This thesis investigates single channel recordings of IKs with and without mutations that cause LQT1 using patch clamp electrophysiology. Single channel IKs is described by slow and fast gating processes. The channel is slow to open, but flickers rapidly between open and closed states in non-deactivating bursts. Long latency periods to opening underlie the slow activation of IKs at depolarized potentials. Channel activity is cyclic with periods of high activity followed by quiescence, leading to an overall low open probability. The mean single channel conductance was determined to be 3.2 pS and long-lived subconductance levels coupled to activation were observed. Single channel properties of IKs with LQT1 mutations in the S3 helix of the voltage sensing domain in KCNQ1 were investigated to uncover pathogenic mechanisms at the single molecule level. Open probability was reduced in loss-of-function mutations (D202H, I204F and V205M) and increased in a unique gain-of-function mutation (S209F) that may cause LQTS from a reduced number of functional channels at the cell surface. The mean duration of open events correlated well with deactivation rate in all mutants and first latency to opening determined activation rate. From these results, we attributed the pathogenic mechanisms of LQT1 mutations to alterations in the stability of specific channel states. Medicine, Faculty of Anesthesiology, Pharmacology and Therapeutics, Department of Graduate 2011-11-15T00:02:03Z 2011-11-15T00:02:03Z 2011 2012-05 Text Thesis/Dissertation http://hdl.handle.net/2429/38968 eng Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ University of British Columbia
collection NDLTD
language English
sources NDLTD
description The slow potassium current, IKs, abbreviates the cardiac action potential by repolarizing the membrane to a resting state. Mutations in the pore-forming IKs subunit, KCNQ1, cause long QT syndrome type 1 (LQT1), which increases risk of fatal arrhythmia. Despite the physiological and clinical importance of IKs, little is known about the elementary events that underlie the unique biophysical properties of the channel, and how these elementary events are altered in the face of disease. This thesis investigates single channel recordings of IKs with and without mutations that cause LQT1 using patch clamp electrophysiology. Single channel IKs is described by slow and fast gating processes. The channel is slow to open, but flickers rapidly between open and closed states in non-deactivating bursts. Long latency periods to opening underlie the slow activation of IKs at depolarized potentials. Channel activity is cyclic with periods of high activity followed by quiescence, leading to an overall low open probability. The mean single channel conductance was determined to be 3.2 pS and long-lived subconductance levels coupled to activation were observed. Single channel properties of IKs with LQT1 mutations in the S3 helix of the voltage sensing domain in KCNQ1 were investigated to uncover pathogenic mechanisms at the single molecule level. Open probability was reduced in loss-of-function mutations (D202H, I204F and V205M) and increased in a unique gain-of-function mutation (S209F) that may cause LQTS from a reduced number of functional channels at the cell surface. The mean duration of open events correlated well with deactivation rate in all mutants and first latency to opening determined activation rate. From these results, we attributed the pathogenic mechanisms of LQT1 mutations to alterations in the stability of specific channel states. === Medicine, Faculty of === Anesthesiology, Pharmacology and Therapeutics, Department of === Graduate
author Werry, Daniel
spellingShingle Werry, Daniel
Single channel properties of the slow cardiac potassium current, IKs
author_facet Werry, Daniel
author_sort Werry, Daniel
title Single channel properties of the slow cardiac potassium current, IKs
title_short Single channel properties of the slow cardiac potassium current, IKs
title_full Single channel properties of the slow cardiac potassium current, IKs
title_fullStr Single channel properties of the slow cardiac potassium current, IKs
title_full_unstemmed Single channel properties of the slow cardiac potassium current, IKs
title_sort single channel properties of the slow cardiac potassium current, iks
publisher University of British Columbia
publishDate 2011
url http://hdl.handle.net/2429/38968
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