Transfer of Rolf S3-S4 Linker to hERG Eliminates Activation Gating but Spares Inactivation

Transfer of Rolf S3-S4 Linker to hERG Eliminates Activation Gating but Spares Inactivation
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DOI:
10.1016/j.bpj.2009.05.060
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发表时间:
2009-09-02
影响因子:
3.4
通讯作者:
Loussouarn, Gildas
Loussouarn, Gildas
中科院分区:
生物学3区
文献类型:
--
作者:
Choveau, Frank S.;El Harchi, Aziza;Loussouarn, Gildas

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Studies in Shaker, a voltage-dependent potassium channel, suggest a coupling between activation and inactivation. This coupling is controversial in hERG, a fast-inactivating voltage-dependent potassium channel. To address this question, we transferred to hERG the S3-S4 linker of the voltage-independent channel, rolf, to selectively disrupt the activation process. This chimera shows an intact voltage-dependent inactivation process consistent with a weak coupling, if any, between both processes. Kinetic models suggest that the chimera presents only an open and an inactivated states, with identical transition rates as in hERG. The lower sensitivity of the chimera to BeKm-1, a hERG preferential closed-state inhibitor, also suggests that the chimera presents mainly open and inactivated conformations. This chimera allows determining the mechanism of action of hERG blockers, as exemplified by the test on ketoconazole.