Key result
Analysis of a novel G protein-activated chimeric inward rectifier channel revealed that single channel activation is explained by a G protein-dependent shift favoring a bursting state.
G protein-dependent activation of inward rectifier potassium channels shifts the equilibrium towards a bursting state, elucidating the mechanism of negative regulation of heartbeat rate.
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Offers single-channel mechanism for G protein heart rate control; leaves open human therapeutic translation.
Negative regulation of the heartbeat rate involves the activation of an inwardly rectifying potassium current (I(KACh)) by G protein-coupled receptors such as the m2 muscarinic acetylcholine receptor. Recent studies have shown that this process involves the direct binding of G(betagamma) subunits to the NH(2)- and COOH-terminal cytoplasmic domains of the proteins termed GIRK1 and GIRK4 (Kir3.1 and Kir3.4/CIR), which mediate I(KACh). Because of the very low basal activity of native I(KACh), it has been difficult to determine the single channel effect of G(betagamma) subunit binding on I(KACh) activity. Through analysis of a novel G protein-activated chimeric inward rectifier channel that displays increased basal activity relative to I(KACh), we find that single channel activation can be explained by a G protein-dependent shift in the equilibrium of open channel transitions in favor of a bursting state of channel activity over a long-lived closed state.
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Bard et al. (2000) studied this question. Analysis of a novel G protein-activated chimeric inward rectifier channel revealed that single channel activation is explained by a G protein-dependent shift favoring a bursting state.
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