Structural changes during C-type inactivation of Shaker K+ channels create high energy barriers that trap Ba2+ within the pore.
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Does not contain clinical trial data; leaves open any cardiac relevance of Ba2+ trapping in K+ channels.
Shaker K+ channels inactivate through two distinct molecular mechanisms: N-type, which involves the N-terminal domain and C-type that appears to involve structural modifications at the external mouth of the channel. We have tested pore accessibility of the Shaker K+ channel during C-type inactivation using Ba2+ as a probe. We determined that external Ba2+ binds to C-type inactivated channels forming an extremely stable complex; i.e. there is Ba2+ trapping by C-type inactivated channels. The structural changes Shaker channels undergo during C-type inactivation create high energy barriers that hinder Ba2+ exit to either the extracellular solution or to the intracellular solution.
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Basso et al. (1998) studied this question.
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