Erratum to "Actions of ATX-II and other gating-modifiers on Na+ currents in HEK-293 cells expressing WT and ΔKPQ hNaV 1.5 Na+ channels" [Toxicon 53 (2009) 78-89] (DOI:10.1016/j.toxicon.2008.10.015);Actions of ATX-II and other gating-modifiers on Na+ currents in HEK-293 cells expressing WT and ΔKPQ hNaV 1.5 Na+ channels

Toxicon

Volumn 53, Issue 1, 2009, Pages 78-89

  Spencer, C Ian ^a  

^a CV THERAPEUTICS INC   (United States)

Author keywords

Channelopathy; Gating modifiers; SCN5A sodium channel; Sea anemone toxins; Steady state inactivation

Indexed keywords

PYRETHROID; SEA ANEMONE TOXIN; VOLTAGE GATED SODIUM CHANNEL;

ARTICLE; CELL STRAIN HEK293; CONTROLLED STUDY; DEPOLARIZATION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEA ANEMONE;

ACTINIARIA;

EID: 57749098574     PISSN: 00410101     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.toxicon.2009.01.008     Document Type: Erratum

References (39)

1. Armstrong C.M., and Gilly W.F. Access resistance and space clamp problems associated with whole-cell patch clamping. Methods Enzymol 207 (1992) 100-122
2. Campos F.V., Chanda B., Beirao P.S., and Bezanilla F. Alpha-scorpion toxin impairs a conformational change that leads to fast inactivation of muscle sodium channels. J. Gen. Physiol 132 (2008) 251-263
3. Carboni M., Zhang Z.S., Neplioueva V., Starmer C.F., and Grant A.O. Slow sodium channel inactivation and use-dependent block modulated by the same domain IV S6 residue. J. Membr. Biol. 207 (2005) 107-117
4. Catterall W.A., Cestele S., Yarov-Yarovoy V., Yu F.H., Konoki K., and Scheuer T. Voltage-gated ion channels and gating modifier toxins. Toxicon 49 (2007) 124-141
5. + channel hNav1.5 is reversed by lysine or glutamine substitution at V930 in D2-S6. Am. J. Physiol. Cell Physiol 293 (2007) C1895-C1905
6. Chandra R., Starmer C.F., and Grant A.O. Multiple effects of KPQ deletion mutation on gating of human cardiac Na+ channels expressed in mammalian cells. Am. J. Physiol 274 (1998) H1643-H1654
7. Chen H., and Heinemann S.H. Interaction of scorpion alpha-toxins with cardiac sodium channels: binding properties and enhancement of slow inactivation. J. Gen. Physiol 117 (2001) 505-518
8. Chen T., and Sheets M.F. Enhancement of closed-state inactivation in long QT syndrome sodium channel mutation DeltaKPQ. Am. J. Physiol. Heart Circ. Physiol 283 (2002) H966-H975
9. Clancy C.E., and Rudy Y. Linking a genetic defect to its cellular phenotype in a cardiac arrhythmia. Nature 400 (1999) 566-569
10. Eaholtz G., Scheuer T., and Catterall W.A. Restoration of inactivation and block of open sodium channels by an inactivation gate peptide. Neuron 12 (1994) 1041-1048
11. Gonoi T., and Hille B. Gating of Na channels. Inactivation modifiers discriminate among models. J. Gen. Physiol 89 (1987) 253-274
12. Hanck D.A., and Sheets M.F. Modification of inactivation in cardiac sodium channels: ionic current studies with Anthopleurin-A toxin. J. Gen. Physiol 106 (1995) 601-616
13. + channel inactivation gating. Circ. Res. 75 (1994) 114-122
14. + channels by DPI 201-106: different voltage-dependencies of the drug actions. Naunyn Schmiedebergs Arch. Pharmacol 335 (1987) 183-188
15. Leibowitz M.D., Sutro J.B., and Hille B. Voltage-dependent gating of veratridine-modified Na channels. J. Gen. Physiol 87 (1986) 25-46
16. Marban E., Yamagishi T., and Tomaselli G.F. Structure and function of voltage-gated sodium channels. J. Physiol 508 Pt 3 (1998) 647-657
17. McPhee J.C., Ragsdale D.S., Scheuer T., and Catterall W.A. A critical role for the S4-S5 intracellular loop in domain IV of the sodium channel alpha-subunit in fast inactivation. J. Biol. Chem. 273 (1998) 1121-1129
18. Medeiros-Domingo A., Kaku T., Tester D.J., Iturralde-Torres P., Itty A., Ye B., Valdivia C., Ueda K., Canizales-Quinteros S., Tusie-Luna M.T., Makielski J.C., and Ackerman M.J. SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome. Circulation 116 (2007) 134-142
19. Mitrovic N., George Jr. A.L., and Horn R. Role of domain 4 in sodium channel slow inactivation. J. Gen. Physiol 115 (2000) 707-718
20. Moran O., Nizzari M., and Conti F. Endogenous expression of the beta1A sodium channel subunit in HEK-293 cells. FEBS Lett. 473 (2000) 132-134
21. Moss, A.J., Zareba, W., Schwarz, K.Q., Rosero, S., McNitt, S., Robinson, J.L., Ranolazine Shortens Repolarization in Patients with Sustained Inward Sodium Current Due to Type-3 Long-QT Syndrome SO: Journal of Cardiovascular Electrophysiology. 2008;9999 (9999): 1045-3873; 1540-8167.
22. + channels. Am. J. Physiol 275 (1998) H2016-H2024
23. Ogata N., and Yoshida S. New perspectives on the structure and function of the Na channel multigene family. Curr. Med. Chem. Central Nervous System Agents 2 (2002) 59-81
24. Oliveira J.S., Redaelli E., Zaharenko A.J., Cassulini R.R., Konno K., Pimenta D.C., Freitas J.C., Clare J.J., and Wanke E. Binding specificity of sea anemone toxins to Nav 1.1-1.6 sodium channels: unexpected contributions from differences in the IV/S3-S4 outer loop. J. Biol. Chem. 279 (2004) 33323-33335
25. + channel alpha subunit. J. Biol. Chem. 271 (1996) 15950-15962
26. + channels as sites of action of the cardioactive agent DPI 201-106 with agonist and antagonist enantiomers. Proc. Natl. Acad. Sci. USA 84 (1987) 896-900
27. Scholtysik G., Quast U., and Schaad A. Evidence for different receptor sites for the novel cardiotonic S-DPI 201-106, ATX II and veratridine on the cardiac sodium channel. Eur. J. Pharmacol 125 (1986) 111-118
28. Sheets M.F., and Hanck D.A. Gating of skeletal and cardiac muscle sodium channels in mammalian cells. J. Physiol 514 Pt 2 (1999) 425-436
29. Sheets M.F., and Hanck D.A. Molecular action of lidocaine on the voltage sensors of sodium channels. J. Gen. Physiol 121 (2003) 163-175
30. Sheets M.F., and Hanck D.A. Charge immobilization of the voltage sensor in domain IV is independent of sodium current inactivation. J. Physiol 563 (2005) 83-93
31. Spencer C.I., and Sham J.S. Mechanisms underlying the effects of the pyrethroid tefluthrin on action potential duration in isolated rat ventricular myocytes. J. Pharmacol. Exp. Ther 315 (2005) 16-23
32. + channels in guinea pig ventricular myocytes. Am. J. Physiol 264 (1993) H454-H463
33. Tan B.H., Iturralde-Torres P., Medeiros-Domingo A., Nava S., Tester D.J., Valdivia C.R., Tusie-Luna T., Ackerman M.J., and Makielski J.C. A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia. Cardiovasc. Res. 76 (2007) 409-417
34. Vais H., Atkinson S., Pluteanu F., Goodson S.J., Devonshire A.L., Williamson M.S., and Usherwood P.N. Mutations of the para sodium channel of Drosophila melanogaster identify putative binding sites for pyrethroids. Mol. Pharmacol 64 (2003) 914-922
35. + channel mutations in the congenital long QT syndrome. Proc. Natl. Acad. Sci. USA 93 (1996) 13200-13205
36. Wang G., Dugas M., Ben Armah I., and Honerjager P. Interaction between DPI 201-106 enantiomers at the cardiac sodium channel. Mol. Pharmacol 37 (1990) 17-24
37. Wang G.K., and Wang S.Y. Veratridine block of rat skeletal muscle Nav1.4 sodium channels in the inner vestibule. J. Physiol 548 (2003) 667-675
38. Wang S.Y., and Wang G.K. Voltage-gated sodium channels as primary targets of diverse lipid-soluble neurotoxins. Cell. Signal 15 (2003) 151-159
39. Yu F.H., and Catterall W.A. Overview of the voltage-gated sodium channel family. Genome Biol. 4 (2003) 207