Key result
Intracellular polyamines and magnesium cause a voltage-dependent block of the inward-rectifier potassium channel pore, resulting in inward-rectification.
Provides a comprehensive overview of the molecular and biophysical mechanisms underlying the inward-rectification of Kir channels by polyamines.
Inward-rectifier potassium (Kir) channels comprise a superfamily of potassium (K+) channels with unique structural and functional properties. Expressed in virtually all types of cells they are responsible for setting the resting membrane potential, controlling the excitation threshold and secreting K+ ions. All Kir channels present an inwardly rectifying current-voltage relation, meaning that at any given driving force the inward flow of K+ ions exceeds the outward flow for the opposite driving force. This inward-rectification is due to a voltage-dependent block of the channel pore by intracellular polyamines and magnesium. The present molecular-biophysical understanding of inward-rectification and its physiological consequences is the topic of this review. In addition to polyamines, Kir channels are gated by intracellular protons, G-proteins, ATP and phospholipids depending on the respective Kir subfamily as detailed in the following review articles.
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Oliver et al. (2000) conducted a review in Inward-rectifier potassium (Kir) channel function. Polyamines was evaluated. Intracellular polyamines and magnesium cause a voltage-dependent block of the inward-rectifier potassium channel pore, resulting in inward-rectification.
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