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Concerted All-or-none Subunit Interactions Mediate Slow Deactivation of Human ether-à-go-go-related Gene K+ Channels
During the repolarization phase of a cardiac action potential, hERG1 K+ channels rapidly recover from an inactivated state then slowly deactivate to a closed state. The resulting resurgence of outward current terminates the plateau phase and is thus a key regulator of action potential duration of ca...
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Published in: | The Journal of biological chemistry 2014-08, Vol.289 (34), p.23428-23436 |
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creator | Thomson, Steven J. Hansen, Angela Sanguinetti, Michael C. |
description | During the repolarization phase of a cardiac action potential, hERG1 K+ channels rapidly recover from an inactivated state then slowly deactivate to a closed state. The resulting resurgence of outward current terminates the plateau phase and is thus a key regulator of action potential duration of cardiomyocytes. The intracellular N-terminal domain of the hERG1 subunit is required for slow deactivation of the channel as its removal accelerates deactivation 10-fold. Here we investigate the stoichiometry of hERG1 channel deactivation by characterizing the kinetic properties of concatenated tetramers containing a variable number of wild-type and mutant subunits. Three mutations known to accelerate deactivation were investigated, including R56Q and R4A/R5A in the N terminus and F656I in the S6 transmembrane segment. In all cases, a single mutant subunit induced the same rapid deactivation of a concatenated channel as that observed for homotetrameric mutant channels. We conclude that slow deactivation gating of hERG1 channels involves a concerted, fully cooperative interaction between all four wild-type channel subunits. |
doi_str_mv | 10.1074/jbc.M114.582437 |
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The resulting resurgence of outward current terminates the plateau phase and is thus a key regulator of action potential duration of cardiomyocytes. The intracellular N-terminal domain of the hERG1 subunit is required for slow deactivation of the channel as its removal accelerates deactivation 10-fold. Here we investigate the stoichiometry of hERG1 channel deactivation by characterizing the kinetic properties of concatenated tetramers containing a variable number of wild-type and mutant subunits. Three mutations known to accelerate deactivation were investigated, including R56Q and R4A/R5A in the N terminus and F656I in the S6 transmembrane segment. In all cases, a single mutant subunit induced the same rapid deactivation of a concatenated channel as that observed for homotetrameric mutant channels. 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The resulting resurgence of outward current terminates the plateau phase and is thus a key regulator of action potential duration of cardiomyocytes. The intracellular N-terminal domain of the hERG1 subunit is required for slow deactivation of the channel as its removal accelerates deactivation 10-fold. Here we investigate the stoichiometry of hERG1 channel deactivation by characterizing the kinetic properties of concatenated tetramers containing a variable number of wild-type and mutant subunits. Three mutations known to accelerate deactivation were investigated, including R56Q and R4A/R5A in the N terminus and F656I in the S6 transmembrane segment. In all cases, a single mutant subunit induced the same rapid deactivation of a concatenated channel as that observed for homotetrameric mutant channels. We conclude that slow deactivation gating of hERG1 channels involves a concerted, fully cooperative interaction between all four wild-type channel subunits.</description><subject>Animals</subject><subject>Ether-A-Go-Go Potassium Channels - chemistry</subject><subject>Ether-A-Go-Go Potassium Channels - genetics</subject><subject>Ether-A-Go-Go Potassium Channels - metabolism</subject><subject>Gene Silencing</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Molecular Biophysics</subject><subject>Mutation</subject><subject>Xenopus laevis</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kcFuVCEUhonR2LG6dmdYmhimwIW5w8akmWrb2MaFmrgjXDi3Q8NABe4Y38Z38cXkZmqjCwkJgfOfD8KH0EtGl4z24uR2sMtrxsRSrrno-kdowei6I51kXx-jBaWcEcXl-gg9K-WWtiEUe4qOuKQtxvkCTZsULeQKDp-GQFImMUXAn6Zhir7iy1ghG1t9igVfg_OmtmJI3_EZzMd7M5dwGvHFtDMRQ91CJr9-kps0zwzBzOhzaMwPb_Bma2KEUJ6jJ6MJBV7cr8foy_t3nzcX5Orj-eXm9IpYIbpKnHUdF8yBUGI0bnDgYHRGOSkMN6rtBJO853JgXKneUjM6Nwxi7ZxcjVJ1x-jtgXs3DTtwFmLNJui77Hcm_9DJeP1vJfqtvkl73bgr2q8a4PU9IKdvE5Sqd75YCMFESFPRTEq54r3q-xY9OURtTqVkGB-uYVTPsnSTpWdZ-iCrdbz6-3UP-T92WkAdAu3LYO8h62I9NF_OZ7BVu-T_C_8NMBmnUQ</recordid><startdate>20140822</startdate><enddate>20140822</enddate><creator>Thomson, Steven J.</creator><creator>Hansen, Angela</creator><creator>Sanguinetti, Michael C.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</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>20140822</creationdate><title>Concerted All-or-none Subunit Interactions Mediate Slow Deactivation of Human ether-à-go-go-related Gene K+ Channels</title><author>Thomson, Steven J. ; Hansen, Angela ; Sanguinetti, Michael C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-dcd3241de494fadbdedefda9d54a2a9ede4152725b12997c0afddbb48dd56f593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Ether-A-Go-Go Potassium Channels - chemistry</topic><topic>Ether-A-Go-Go Potassium Channels - genetics</topic><topic>Ether-A-Go-Go Potassium Channels - metabolism</topic><topic>Gene Silencing</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Molecular Biophysics</topic><topic>Mutation</topic><topic>Xenopus laevis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thomson, Steven J.</creatorcontrib><creatorcontrib>Hansen, Angela</creatorcontrib><creatorcontrib>Sanguinetti, Michael C.</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>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thomson, Steven J.</au><au>Hansen, Angela</au><au>Sanguinetti, Michael C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Concerted All-or-none Subunit Interactions Mediate Slow Deactivation of Human ether-à-go-go-related Gene K+ Channels</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2014-08-22</date><risdate>2014</risdate><volume>289</volume><issue>34</issue><spage>23428</spage><epage>23436</epage><pages>23428-23436</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>During the repolarization phase of a cardiac action potential, hERG1 K+ channels rapidly recover from an inactivated state then slowly deactivate to a closed state. 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subjects | Animals Ether-A-Go-Go Potassium Channels - chemistry Ether-A-Go-Go Potassium Channels - genetics Ether-A-Go-Go Potassium Channels - metabolism Gene Silencing Humans Kinetics Molecular Biophysics Mutation Xenopus laevis |
title | Concerted All-or-none Subunit Interactions Mediate Slow Deactivation of Human ether-à-go-go-related Gene K+ Channels |
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