ArticleThe Journal of physiology1998
Voltage change-induced gating transitions of the rabbit skeletal muscle Ca2+ release channel.
Article in The Journal of physiology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 11 citations in OpenAlex.
- BK in Double-Membrane Organelles: A Biophysical, Pharmacological, and Functional Survey.Frontiers in physiology · 2021Review
- Nuclear BK channels regulate gene expression via the control of nuclear calcium signaling.Nature neuroscience · 2014Article
- Nuclear KATP channels trigger nuclear Ca(2+) transients that modulate nuclear function.Proceedings of the National Academy of Sciences of the United States of America · 2002Article
- Questions about adaptation in ryanodine receptors.The Journal of general physiology · 2000Review
- Oxidation and reduction of pig skeletal muscle ryanodine receptors.Biophysical journal · 1999Article
Corrections and comments
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Authors and funding
2 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
1. We used the planar lipid bilayer method to study single ryanodine receptor Ca2+ release channels (RyRCs) from fast skeletal muscle of the rabbit. We found that changes in membrane voltage directly induced gating transitions of the RyRC: (i) in the steady state, even at activating Ca2+ concentrations (20 microM), at a constant membrane potential the channels resided in a low open probability (Po) state (inactivated-, I-mode), and (ii) upon abrupt changes of voltage, the apparent inactivation of the RyRCs was relieved, resulting in a rapid and transient increase in Po. 2. The magnitude of the Po increase was a function of both the duration and the amplitude of the applied prepulse, but was independent of the channel activity during the prepulse. 3. The voltage-induced Po increase probably involved major conformational changes of the channel, as it resulted in substantial alterations in the gating pattern of the channels: the voltage change-induced increase in Po was accompanied by the rapid appearance of two types of channel activity (high (H) and low (L) open probability modes). 4. The response of the RyRC to voltage changes raises the interesting possibility that the activation of RyRC in situ might involve electrical events, i.e. a possible dipole-dipole coupling between the release channel and the voltage sensor.
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