Molecular interactions between two long-QT syndrome gene products, HERG and KCNE2, rationalized by in vitro and in silico analysis. Export

@article{Mazhari2001_HERG_model, abstract = {The cardiac delayed rectifier potassium current mediates repolarization of the action potential and underlies the QT interval of the ECG. Mutations in either of the two molecular components of the rapid delayed rectifier (I(K,r)), HERG and KCNE2, have been linked to heritable or acquired long-QT syndrome. Mechanisms whereby mutations of KCNE2 produce fatal cardiac arrhythmias characteristic of long-QT syndrome remain unclear. In this study, we characterize functional interactions between HERG and KCNE2 with a view to defining underlying mechanisms for action potential prolongation and long-QT syndrome. Whereas coexpression of hKCNE2 with HERG alters both kinetics and density of ionic current, incorporation of these effects into a quantitative model of the action potential predicts that only changes in current density significantly affect repolarization. Thus, the primary functional consequence of hKCNE2 on action potential morphology is through modulation of I(K,r) density, as predicted by the model. Mutations associated with long-QT syndrome that result only in modest changes of gating kinetics may be epiphenomena or may modulate action potential repolarization via interaction with alternative pore-forming potassium channel alpha subunits.}, address = {Department of Medicine, Institute of Molecular Cardiobiology, Johns Hopkins University, Baltimore, MD 21205, USA.}, author = {Mazhari, R. and Greenstein, J. L. and Winslow, R. L. and Marb\'{a}n, E. and Nuss, H. B.}, citeulike-article-id = {1102237}, citeulike-linkout-0 = {http://view.ncbi.nlm.nih.gov/pubmed/11440975}, citeulike-linkout-1 = {http://www.hubmed.org/display.cgi?uids=11440975}, day = {6}, issn = {1524-4571}, journal = {Circ Res}, keywords = {herg, model}, month = {July}, number = {1}, pages = {33--38}, posted-at = {2007-02-12 07:20:43}, priority = {0}, title = {Molecular interactions between two long-QT syndrome gene products, HERG and KCNE2, rationalized by in vitro and in silico analysis.}, url = {http://view.ncbi.nlm.nih.gov/pubmed/11440975}, volume = {89}, year = {2001} }

TY - JOUR ID - Mazhari2001_HERG_model L3 - citeulike-article-id:1102237 N2 - The cardiac delayed rectifier potassium current mediates repolarization of the action potential and underlies the QT interval of the ECG. Mutations in either of the two molecular components of the rapid delayed rectifier (I(K,r)), HERG and KCNE2, have been linked to heritable or acquired long-QT syndrome. Mechanisms whereby mutations of KCNE2 produce fatal cardiac arrhythmias characteristic of long-QT syndrome remain unclear. In this study, we characterize functional interactions between HERG and KCNE2 with a view to defining underlying mechanisms for action potential prolongation and long-QT syndrome. Whereas coexpression of hKCNE2 with HERG alters both kinetics and density of ionic current, incorporation of these effects into a quantitative model of the action potential predicts that only changes in current density significantly affect repolarization. Thus, the primary functional consequence of hKCNE2 on action potential morphology is through modulation of I(K,r) density, as predicted by the model. Mutations associated with long-QT syndrome that result only in modest changes of gating kinetics may be epiphenomena or may modulate action potential repolarization via interaction with alternative pore-forming potassium channel alpha subunits. IS - 1 JF - Circ Res SN - 1524-4571 AD - Department of Medicine, Institute of Molecular Cardiobiology, Johns Hopkins University, Baltimore, MD 21205, USA. EP - 38 TI - Molecular interactions between two long-QT syndrome gene products, HERG and KCNE2, rationalized by in vitro and in silico analysis. VL - 89 SP - 33 KW - herg KW - model AU - Mazhari, R AU - Greenstein, JL AU - Winslow, RL AU - Marbán, E AU - Nuss, HB PY - 2001/07/06/ UR - http://view.ncbi.nlm.nih.gov/pubmed/11440975 ER -