期刊
CARDIOVASCULAR RESEARCH
卷 54, 期 1, 页码 67-76出版社
OXFORD UNIV PRESS
DOI: 10.1016/S0008-6363(02)00240-7
关键词
arrhythmia (mechanisms); K-channel; long QT syndrome
Objective: In a 32-year-old woman with marked QT prolongation (QTc=0.61 s) and repeated episodes of syncope, we identified a single pertinent base substitution (G to A at 1909) in HERG by genetic analysis. This novel missense mutation is predicted to cause an amino acid substitution of lysine for glutamic acid at position 637 (E637K) in the pore-S6 loop. Therefore, we investigated the role of a glutamic acid at the vicinity of the pore in HERG channels by mutating it to a lysine. Methods: We characterized the electrophysiological properties of the E637K mutation using a Xenopus oocyte heterologous expression system. Results: Injection of the E637K mutant cRNA alone into Xenopus oocytes did not result in any expression of detectable currents. Coexpression of wild-type (WT) and E637K (E637K/WT) elicited only about 30% of the control peak tail current that was expected from expression of WT alone. Kinetic analyses revealed that E637K/WT decelerated the rate of channel activation and enhanced steady-state inactivation. Furthermore, the reversal potentials at low concentrations of K. showed a positive shift in oocytes injected with E637K/WT compared with WT alone. Conclusions: These results indicated that the E637K mutation causes apparent dominant negative suppression of WT HERG channel function and suggest that E637 at the Pore-S6 is a crucial component of the activation and inactivation gate of HERG channels. (C) 2002 Elsevier Science B.V. All rights reserved.
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