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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
1991-7-2
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pubmed:abstractText |
Na+ permeation through normal and batrachotoxin (BTX)-modified squid axon Na+ channels was characterized. Unmodified and toxin-modified Na+ channels were studied simultaneously in outside-out membrane patches using the cut-open axon technique. Current-voltage relations for both normal and BTX-modified channels were measured over a wide range of Na+ concentrations and voltages. Channel conductance as a function of Na+ concentration curves showed that within the range 0.015-1 M Na+ the normal channel conductance is 1.7-2.5-fold larger than the BTX-modified conductance. These relations cannot be fitted by a simple Langmuir isotherm. Channel conductance at low concentrations was larger than expected from a Michaelis-Menten behavior. The deviations from the simple case were accounted for by fixed negative charges located in the vicinity of the channel entrances. Fixed negative charges near the pore mouths would have the effect of increasing the local Na+ concentration. The results are discussed in terms of energy profiles with three barriers and two sites, taking into consideration the effect of the fixed negative charges. Either single- or multi-ion pore models can account for all the permeation data obtained in both symmetric and asymmetric conditions. In a temperature range of 5-15 degrees C, the estimated Q10 for the conductance of the BTX-modified Na+ channel was 1.53. BTX appears not to change the Na+ channel ion selectively (for the conditions used) or the surface charge located near the channel entrances.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/1645396-1168643,
http://linkedlifedata.com/resource/pubmed/commentcorrection/1645396-1194886,
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http://linkedlifedata.com/resource/pubmed/commentcorrection/1645396-6965422
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1295
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
97
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
605-25
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:1645396-Animals,
pubmed-meshheading:1645396-Axons,
pubmed-meshheading:1645396-Batrachotoxins,
pubmed-meshheading:1645396-Biological Transport, Active,
pubmed-meshheading:1645396-Decapodiformes,
pubmed-meshheading:1645396-Electrophysiology,
pubmed-meshheading:1645396-Models, Biological,
pubmed-meshheading:1645396-Sodium,
pubmed-meshheading:1645396-Sodium Channels,
pubmed-meshheading:1645396-Temperature
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pubmed:year |
1991
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pubmed:articleTitle |
Ion permeation in normal and batrachotoxin-modified Na+ channels in the squid giant axon.
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pubmed:affiliation |
Department of Physiology, Ahmanson Laboratory of Neurobiology, University of California, Los Angeles 90024.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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