The voltage-gated Na+ channel is the central determinant of muscle excitability. There are seven human disorders associated with gene defects in the Na+ channel or its subunits including the Long QT Syndrome and idiopathic ventricular fibrillation. Drugs that act upon Na+ channels including anticonvulsants, local anesthetics, and antiarrhythmic agents.
The aim of the proposed project is to test, refine, and expand a molecular model of the outer vestibule and selectivity filter of the Na+ channel as part of larger effort to understand the structural biology of this channel. Detailed structural information will be necessary to fully understand the function of the channel, to engage in rational drug design, and to consider the possibility of protein engineering in conjunction with gene therapy to ameliorate genetic diseases linked to the Na+ channel. The hypothesis being tested is that a detailed molecular model of a complementary binding surface can be constructed by determining sufficient ligand/substrate interaction points using several ligands of known structure. The experiments will evaluate, refine, and expand a previously described Na+ channel outer vestibule model by testing predictions about the points of interaction with high affinity ligands that bind in this area. The approach is general for ligand/receptor interactions, and an analogy for this approach would be a lock and key where the ligands are the keys and the Na+ channel is the lock. The structure of the lock is determined by looking at the shape of the keys. Specifically, points of interaction between channel amino acids and the ligands will be determined using mutant cycle analysis. The shape of the ligands and the points of interaction are used as constraints when refining computer-generated models of the binding surface. Multiple toxins will used to probe as much of the outer vestibule as possible, to serve as validation of results obtain with other ligands, and to develop sufficient interaction points to constrain adequately the model.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL064828-05
Application #
6746953
Study Section
Cardiovascular and Renal Study Section (CVB)
Program Officer
Wang, Lan-Hsiang
Project Start
2000-06-10
Project End
2005-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
5
Fiscal Year
2004
Total Cost
$155,800
Indirect Cost
Name
Emory University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Shang, Lijuan L; Gao, Ge; Dudley Jr, Samuel C (2008) The tail of the cardiac sodium channel. Channels (Austin) 2:161-2
Shang, Lijuan L; Sanyal, Shamarendra; Pfahnl, Arnold E et al. (2008) NF-kappaB-dependent transcriptional regulation of the cardiac scn5a sodium channel by angiotensin II. Am J Physiol Cell Physiol 294:C372-9
Choudhary, Gaurav; Aliste, Marcela P; Tieleman, D Peter et al. (2007) Docking of mu-conotoxin GIIIA in the sodium channel outer vestibule. Channels (Austin) 1:344-52
Pfahnl, Arnold E; Viswanathan, Prakash C; Weiss, Raul et al. (2007) A sodium channel pore mutation causing Brugada syndrome. Heart Rhythm 4:46-53
Shang, Lijuan L; Pfahnl, Arnold E; Sanyal, Shamarendra et al. (2007) Human heart failure is associated with abnormal C-terminal splicing variants in the cardiac sodium channel. Circ Res 101:1146-54
Kasi, Vijaykumar S; Xiao, Hong D; Shang, Lijuan L et al. (2007) Cardiac-restricted angiotensin-converting enzyme overexpression causes conduction defects and connexin dysregulation. Am J Physiol Heart Circ Physiol 293:H182-92
Shang, Lijuan L; Dudley Jr, Samuel C; Pfahnl, Arnold E (2006) Analysis of arrhythmic potential of embryonic stem cell-derived cardiomyocytes. Methods Mol Biol 330:221-31
Boulden, Beth M; Widder, Julian D; Allen, Jon C et al. (2006) Early determinants of H2O2-induced endothelial dysfunction. Free Radic Biol Med 41:810-7
Dudley Jr, Samuel C (2005) Beware of cells bearing gifts: cell replacement therapy and arrhythmic risk. Circ Res 97:99-101
Shang, Lijuan L; Dudley Jr, Samuel C (2005) Tandem promoters and developmentally regulated 5'- and 3'-mRNA untranslated regions of the mouse Scn5a cardiac sodium channel. J Biol Chem 280:933-40

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