There is increasing awareness of the importance of ion channel accessory proteins in regulating heart rhythm. MinK and the related MiRPs are K+ channel regulators encoded by the KCNE family of genes. They can interact with the two Long QT-associated delayed rectifiers (HERG and KvLQT1 ), pacemaker channels (HCNs) and a variety of voltage gated K+ channels. Their importance is underscored by linkage to hereditary Long QT syndrome and single nucleotide polymorphisms that may sensitize patients to drug-induced arrhythmias. KCNEs each encode small integral membrane proteins with a single transmembrane segment suggesting that they interact with K+ channels in homologous fashion. Their sequence homology however, is fairly divergent with only scattered areas of conservation. Mutations have shown us several of the important sites in KCNE1 & 2 required for function. Controversy remains regarding structure-function relations, stoichiometry and specific protein-protein interactions in vivo. By studying the precise mechanisms of KCNE-channel interaction, a deeper understanding of LQTS, drug-induced and acquired arrhythmias may be gained. To this end we propose to: 1) Determine the specific regions of KvLQT1 and HERG that physically and functionally interact with minK and/or MiRPs. 2) Determine the relative preferences in partners between minK/MiRPs and HERG or KvLQTI. 3) Determine channel complex stoichiometry using epitope-tagged KCNEs and chimeras in biochemical and electrophysiological studies. 4) Analyze the co-expression pattern of minK/MiRPs against that of HERG and KvLQT1 and their association in cardiac myocytes.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL075615-04
Application #
7159331
Study Section
Cardiovascular and Renal Study Section (CVB)
Program Officer
Lathrop, David A
Project Start
2003-12-15
Project End
2008-11-30
Budget Start
2006-12-01
Budget End
2008-11-30
Support Year
4
Fiscal Year
2007
Total Cost
$395,865
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
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Chen, Jerri; Zheng, Renjian; Melman, Yonathan F et al. (2009) Functional interactions between KCNE1 C-terminus and the KCNQ1 channel. PLoS One 4:e5143
Li, Yan; Um, Sung Yon; McDonald, Thomas V (2006) Voltage-gated potassium channels: regulation by accessory subunits. Neuroscientist 12:199-210
Melman, Yonathan F; Um, Sung Yon; Krumerman, Andrew et al. (2004) KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity. Neuron 42:927-37