Ion effects on gating of the Ca(2+)-activated K+ channel correlate with occupancy of the pore
We studied the effects of permeant ions on the gating of the large conductance Ca(2+)-activated K+ channel from rat skeletal muscle. Rb+ blockade of inward K+ current caused an increase in the open probability as though Rb+ occupancy of the pore interferes with channel closing. In support of this hy...
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Veröffentlicht in: | Biophysical journal 1992-03, Vol.61 (3), p.639-648 |
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description | We studied the effects of permeant ions on the gating of the large conductance Ca(2+)-activated K+ channel from rat skeletal muscle. Rb+ blockade of inward K+ current caused an increase in the open probability as though Rb+ occupancy of the pore interferes with channel closing. In support of this hypothesis, we directly measured the occupancy of the pore by the impermeant ion Cs+ and found that it strongly correlates with its effect on gating. This is consistent with the "foot-in-the-door" model of gating, which states that channels cannot close with an ion in the pore. However, because Rb+ and Cs+ not only slow the closing rate (as predicted by the model), but also speed the opening rate, our results are more consistent with a modified version of the model in which the channel can indeed close while occupied, but the occupancy destabilizes the closed state. Increasing the occupancy of the pore by the addition of other permeant (K+ and Tl+) and impermeant (tetraethylammonium) ions did not affect the open probability. To account for this disparity, we used a two-site permeation model in which only one of the sites influenced gating. Occupancy of this "gating site" interferes with channel closing and hastens opening. Ions that directly or indirectly increase the occupancy of this site will increase the open probability. |
doi_str_mv | 10.1016/S0006-3495(92)81869-6 |
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Rb+ blockade of inward K+ current caused an increase in the open probability as though Rb+ occupancy of the pore interferes with channel closing. In support of this hypothesis, we directly measured the occupancy of the pore by the impermeant ion Cs+ and found that it strongly correlates with its effect on gating. This is consistent with the "foot-in-the-door" model of gating, which states that channels cannot close with an ion in the pore. However, because Rb+ and Cs+ not only slow the closing rate (as predicted by the model), but also speed the opening rate, our results are more consistent with a modified version of the model in which the channel can indeed close while occupied, but the occupancy destabilizes the closed state. Increasing the occupancy of the pore by the addition of other permeant (K+ and Tl+) and impermeant (tetraethylammonium) ions did not affect the open probability. To account for this disparity, we used a two-site permeation model in which only one of the sites influenced gating. Occupancy of this "gating site" interferes with channel closing and hastens opening. Ions that directly or indirectly increase the occupancy of this site will increase the open probability.</description><identifier>ISSN: 0006-3495</identifier><identifier>EISSN: 1542-0086</identifier><identifier>DOI: 10.1016/S0006-3495(92)81869-6</identifier><identifier>PMID: 1504240</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Calcium - pharmacology ; Cell Membrane - physiology ; Cesium - pharmacology ; Electrophysiology - methods ; Ion Channel Gating - drug effects ; Membrane Potentials - drug effects ; Muscles - physiology ; Potassium - pharmacology ; Potassium Channels - drug effects ; Potassium Channels - physiology ; Probability ; Rats ; Rubidium - pharmacology ; Tetraethylammonium ; Tetraethylammonium Compounds - pharmacology ; Thallium - pharmacology</subject><ispartof>Biophysical journal, 1992-03, Vol.61 (3), p.639-648</ispartof><rights>1992 The Biophysical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3776-ac7bf1e677bad871f3b2e3c437ea6206ac83eb6daf38019b9dcf515a42303ad83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1260282/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006349592818696$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3537,27901,27902,53766,53768,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1504240$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Demo, S.D.</creatorcontrib><creatorcontrib>Yellen, G.</creatorcontrib><title>Ion effects on gating of the Ca(2+)-activated K+ channel correlate with occupancy of the pore</title><title>Biophysical journal</title><addtitle>Biophys J</addtitle><description>We studied the effects of permeant ions on the gating of the large conductance Ca(2+)-activated K+ channel from rat skeletal muscle. Rb+ blockade of inward K+ current caused an increase in the open probability as though Rb+ occupancy of the pore interferes with channel closing. In support of this hypothesis, we directly measured the occupancy of the pore by the impermeant ion Cs+ and found that it strongly correlates with its effect on gating. This is consistent with the "foot-in-the-door" model of gating, which states that channels cannot close with an ion in the pore. However, because Rb+ and Cs+ not only slow the closing rate (as predicted by the model), but also speed the opening rate, our results are more consistent with a modified version of the model in which the channel can indeed close while occupied, but the occupancy destabilizes the closed state. Increasing the occupancy of the pore by the addition of other permeant (K+ and Tl+) and impermeant (tetraethylammonium) ions did not affect the open probability. To account for this disparity, we used a two-site permeation model in which only one of the sites influenced gating. Occupancy of this "gating site" interferes with channel closing and hastens opening. Ions that directly or indirectly increase the occupancy of this site will increase the open probability.</description><subject>Animals</subject><subject>Calcium - pharmacology</subject><subject>Cell Membrane - physiology</subject><subject>Cesium - pharmacology</subject><subject>Electrophysiology - methods</subject><subject>Ion Channel Gating - drug effects</subject><subject>Membrane Potentials - drug effects</subject><subject>Muscles - physiology</subject><subject>Potassium - pharmacology</subject><subject>Potassium Channels - drug effects</subject><subject>Potassium Channels - physiology</subject><subject>Probability</subject><subject>Rats</subject><subject>Rubidium - pharmacology</subject><subject>Tetraethylammonium</subject><subject>Tetraethylammonium Compounds - pharmacology</subject><subject>Thallium - pharmacology</subject><issn>0006-3495</issn><issn>1542-0086</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9PFDEUxxuigQX5E0h6IhAy8tpOOzMXjdmgEkk4qEfTdDqvuyWz7drOruG_t7CIePLUpt8fr3kfQk4YvGXA1OVXAFCVqDt51vHzlrWqq9QemTFZ8wqgVa_I7NlyQA5zvgNgXALbJ_tMQs1rmJEf1zFQdA7tlGm5Lszkw4JGR6cl0rk54xfnlbGT35oJB_rlgtqlCQFHamNKOJZX-stPSxqt3axNsPd_suuY8A157cyY8fjpPCLfP159m3-ubm4_Xc8_3FRWNI0q_U3vGKqm6c3QNsyJnqOwtWjQKA7K2FZgrwbjRAus67vBOsmkqbkAURLiiLzb9a43_QoHi2FKZtTr5Fcm3etovP5XCX6pF3GrGVfAW14KTp8KUvy5wTzplc8Wx9EEjJusG8EEk7IuRrkz2hRzTuiehzDQD1z0Ixf9sHTdcf3IRauSO3n5w7-pHYiiv9_pWNa09Zh0th6DxcGnwkYP0f9nwm8T952N</recordid><startdate>19920301</startdate><enddate>19920301</enddate><creator>Demo, S.D.</creator><creator>Yellen, G.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19920301</creationdate><title>Ion effects on gating of the Ca(2+)-activated K+ channel correlate with occupancy of the pore</title><author>Demo, S.D. ; Yellen, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3776-ac7bf1e677bad871f3b2e3c437ea6206ac83eb6daf38019b9dcf515a42303ad83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Animals</topic><topic>Calcium - pharmacology</topic><topic>Cell Membrane - physiology</topic><topic>Cesium - pharmacology</topic><topic>Electrophysiology - methods</topic><topic>Ion Channel Gating - drug effects</topic><topic>Membrane Potentials - drug effects</topic><topic>Muscles - physiology</topic><topic>Potassium - pharmacology</topic><topic>Potassium Channels - drug effects</topic><topic>Potassium Channels - physiology</topic><topic>Probability</topic><topic>Rats</topic><topic>Rubidium - pharmacology</topic><topic>Tetraethylammonium</topic><topic>Tetraethylammonium Compounds - pharmacology</topic><topic>Thallium - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Demo, S.D.</creatorcontrib><creatorcontrib>Yellen, G.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biophysical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Demo, S.D.</au><au>Yellen, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ion effects on gating of the Ca(2+)-activated K+ channel correlate with occupancy of the pore</atitle><jtitle>Biophysical journal</jtitle><addtitle>Biophys J</addtitle><date>1992-03-01</date><risdate>1992</risdate><volume>61</volume><issue>3</issue><spage>639</spage><epage>648</epage><pages>639-648</pages><issn>0006-3495</issn><eissn>1542-0086</eissn><abstract>We studied the effects of permeant ions on the gating of the large conductance Ca(2+)-activated K+ channel from rat skeletal muscle. Rb+ blockade of inward K+ current caused an increase in the open probability as though Rb+ occupancy of the pore interferes with channel closing. In support of this hypothesis, we directly measured the occupancy of the pore by the impermeant ion Cs+ and found that it strongly correlates with its effect on gating. This is consistent with the "foot-in-the-door" model of gating, which states that channels cannot close with an ion in the pore. However, because Rb+ and Cs+ not only slow the closing rate (as predicted by the model), but also speed the opening rate, our results are more consistent with a modified version of the model in which the channel can indeed close while occupied, but the occupancy destabilizes the closed state. Increasing the occupancy of the pore by the addition of other permeant (K+ and Tl+) and impermeant (tetraethylammonium) ions did not affect the open probability. To account for this disparity, we used a two-site permeation model in which only one of the sites influenced gating. Occupancy of this "gating site" interferes with channel closing and hastens opening. Ions that directly or indirectly increase the occupancy of this site will increase the open probability.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>1504240</pmid><doi>10.1016/S0006-3495(92)81869-6</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Calcium - pharmacology Cell Membrane - physiology Cesium - pharmacology Electrophysiology - methods Ion Channel Gating - drug effects Membrane Potentials - drug effects Muscles - physiology Potassium - pharmacology Potassium Channels - drug effects Potassium Channels - physiology Probability Rats Rubidium - pharmacology Tetraethylammonium Tetraethylammonium Compounds - pharmacology Thallium - pharmacology |
title | Ion effects on gating of the Ca(2+)-activated K+ channel correlate with occupancy of the pore |
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