Abstract
The alpha 1 subunit of cardiac Ca2+ channel, expressed alone or coexpressed with the corresponding beta subunit in Xenopus laevis oocytes, elicits rapidly inactivating Ca2+ currents. The inactivation has the following properties: 1) It is practically absent in external Ba2+; 2) it increases with Ca2+ current amplitudes; 3) it is faster at more negative potentials for comparable Ca2+ current amplitudes; 4) it is independent of channel density; and 5) it does not require the beta subunit. These findings indicate that the Ca2+ binding site responsible for inactivation is encoded in the alpha 1 subunit and suggest that it is located near the inner channel mouth but outside the membrane electric field.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Alternative Splicing
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Animals
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Barium / pharmacology
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Calcium / pharmacology*
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Calcium Channel Blockers / pharmacology*
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Calcium Channels / biosynthesis
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Calcium Channels / physiology*
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Cloning, Molecular
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Egtazic Acid / analogs & derivatives
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Egtazic Acid / pharmacology
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Electric Conductivity / drug effects
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Female
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In Vitro Techniques
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Macromolecular Substances
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Membrane Potentials / drug effects
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Membrane Potentials / physiology
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Myocardium / metabolism*
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Oocytes / drug effects
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Oocytes / physiology*
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Recombinant Proteins / biosynthesis
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Recombinant Proteins / metabolism
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Xenopus laevis
Substances
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Calcium Channel Blockers
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Calcium Channels
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Macromolecular Substances
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Recombinant Proteins
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Barium
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Egtazic Acid
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1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid
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Calcium