ArticleThe Journal of general physiology2014
K⁺ channel gating: C-type inactivation is enhanced by calcium or lanthanum outside.
Article in The Journal of general physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed.
- Honeybee CaV4 has distinct permeation, inactivation, and pharmacology from homologous NaV channels.The Journal of general physiology · 2024Article
- Eukaryotic Kv channel Shaker inactivates through selectivity filter dilation rather than collapse.Science advances · 2023Article
- Mechanism of external K+ sensitivity of KCNQ1 channels.The Journal of general physiology · 2023Article
- Structure of the Shaker Kv channel and mechanism of slow C-type inactivation.Science advances · 2022Article
- A unique mechanism of inactivation gating of the Kv channel family member Kv7.1 and its modulation by PIP2 and calmodulin.Science advances · 2020Article
- Synaptic cleft microenvironment influences potassium permeation and synaptic transmission in hair cells surrounded by calyx afferents in the turtle.The Journal of physiology · 2020Article
- Conduction through a narrow inward-rectifier KThe Journal of general physiology · 2019Article
- Single-particle cryo-EM structure of a voltage-activated potassium channel in lipid nanodiscs.eLife · 2018Article
- Crystal structure of an inactivated mutant mammalian voltage-gated KNature structural & molecular biology · 2017Article
- Unambiguous observation of blocked states reveals altered, blocker-induced, cardiac ryanodine receptor gating.Scientific reports · 2016Article
- Reciprocal voltage sensor-to-pore coupling leads to potassium channel C-type inactivation.Scientific reports · 2016Article
- Individual Ion Binding Sites in the K(+) Channel Play Distinct Roles in C-type Inactivation and in Recovery from Inactivation.Structure (London, England : 1993) · 2016Article
- Voltage-Gated Potassium Channels: A Structural Examination of Selectivity and Gating.Cold Spring Harbor perspectives in biology · 2016Review
- Packaging life: the origin of ion-selective channels.Biophysical journal · 2015Review
- Proton transfer unlocks inactivation in cyclic nucleotide-gated A1 channels.The Journal of physiology · 2015Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
Many voltage-gated K(+) channels exhibit C-type inactivation. This typically slow process has been hypothesized to result from dilation of the outer-most ring of the carbonyls in the selectivity filter, destroying this ring's ability to bind K(+) with high affinity. We report here strong enhancement of C-type inactivation upon extracellular addition of 10-40 mM Ca(2+) or 5-50 µM La(3+). These multivalent cations mildly increase the rate of C-type inactivation during depolarization and markedly promote inactivation and/or suppress recovery when membrane voltage (V(m)) is at resting levels (-80 to -100 mV). At -80 mV with 40 mM Ca(2+) and 0 mM K(+) externally, ShBΔN channels with the mutation T449A inactivate almost completely within 2 min or less with no pulsing. This behavior is observed only in those mutants that show C-type inactivation on depolarization and is distinct from the effects of Ca(2+) and La(3+) on activation (opening and closing of the V(m)-controlled gate), i.e., slower activation of K(+) channels and a positive shift of the mid-voltage of activation. The Ca(2+)/La(3+) effects on C-type inactivation are antagonized by extracellular K(+) in the low millimolar range. This, together with the known ability of Ca(2+) and La(3+) to block inward current through K(+) channels at negative voltage, strongly suggests that Ca(2+)/La(3+) acts at the outer mouth of the selectivity filter. We propose that at -80 mV, Ca(2+) or La(3+) ions compete effectively with K(+) at the channel's outer mouth and prevent K(+) from stabilizing the filter's outer carbonyl ring.
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