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Cavβ-subunit displacement is a key step to induce the reluctant state of P/Q calcium channels by direct G protein regulation
P/Q Ca 2+ channel activity is inhibited by G protein-coupled receptor activation. Channel inhibition requires a direct Gβγ binding onto the pore-forming subunit, Ca v 2.1. It is characterized by biophysical changes, including current amplitude reduction, activation kinetic slowing, and an I-V curve...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2004-04, Vol.101 (16), p.6267-6272 |
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container_title | Proceedings of the National Academy of Sciences - PNAS |
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creator | Sandoz, Guillaume Lopez-Gonzalez, Ignacio Grunwald, Didier Bichet, Delphine Altafaj, Xavier Weiss, Norbert Ronjat, Michel Dupuis, Alain De Waard, Michel |
description | P/Q Ca 2+ channel activity is inhibited by G protein-coupled receptor activation. Channel inhibition requires a direct Gβγ binding onto the pore-forming subunit, Ca v 2.1. It is characterized by biophysical changes, including current amplitude reduction, activation kinetic slowing, and an I-V curve shift, which leads to a reluctant mode. Here, we have characterized the contribution of the auxiliary β 3 -subunit to channel regulation by G proteins. The shift in I-V to a P/Q reluctant mode is exclusively observed in the presence of β 3 . Along with the observation that Gβγ has no effect on the I-V curve of Ca v 2.1 alone, we propose that the reluctant mode promoted by Gβγ corresponds to a state in which the β 3 -subunit has been displaced from its channel-binding site. We validate this hypothesis with a β 3 -I-II 2.1 loop chimera construct. Gβγ binding onto the I-II 2.1 loop portion of the chimera releases the β 3 -binding domain and makes it available for binding onto the I-II loop of Ca v 1.2, a G protein-insensitive channel. This finding is extended to the full-length Ca v 2.1 channel by using fluorescence resonance energy transfer. Gβγ injection into Xenopus oocytes displaces a Cy3-labeled β 3 -subunit from a GFP-tagged Ca v 2.1 channel. We conclude that β-subunit dissociation from the channel complex constitutes a key step in P/Q calcium channel regulation by G proteins that underlies the reluctant state and is an important process for modulating neurotransmission through G protein-coupled receptors. |
doi_str_mv | 10.1073/pnas.0306804101 |
format | article |
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Channel inhibition requires a direct Gβγ binding onto the pore-forming subunit, Ca v 2.1. It is characterized by biophysical changes, including current amplitude reduction, activation kinetic slowing, and an I-V curve shift, which leads to a reluctant mode. Here, we have characterized the contribution of the auxiliary β 3 -subunit to channel regulation by G proteins. The shift in I-V to a P/Q reluctant mode is exclusively observed in the presence of β 3 . Along with the observation that Gβγ has no effect on the I-V curve of Ca v 2.1 alone, we propose that the reluctant mode promoted by Gβγ corresponds to a state in which the β 3 -subunit has been displaced from its channel-binding site. We validate this hypothesis with a β 3 -I-II 2.1 loop chimera construct. Gβγ binding onto the I-II 2.1 loop portion of the chimera releases the β 3 -binding domain and makes it available for binding onto the I-II loop of Ca v 1.2, a G protein-insensitive channel. This finding is extended to the full-length Ca v 2.1 channel by using fluorescence resonance energy transfer. Gβγ injection into Xenopus oocytes displaces a Cy3-labeled β 3 -subunit from a GFP-tagged Ca v 2.1 channel. We conclude that β-subunit dissociation from the channel complex constitutes a key step in P/Q calcium channel regulation by G proteins that underlies the reluctant state and is an important process for modulating neurotransmission through G protein-coupled receptors.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0306804101</identifier><identifier>PMID: 15071190</identifier><language>eng</language><publisher>National Acad Sciences</publisher><subject>Biological Sciences</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (16), p.6267-6272</ispartof><rights>Copyright © 2004, The National Academy of Sciences 2004</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/101/16.cover.gif</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC395958/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC395958/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Sandoz, Guillaume</creatorcontrib><creatorcontrib>Lopez-Gonzalez, Ignacio</creatorcontrib><creatorcontrib>Grunwald, Didier</creatorcontrib><creatorcontrib>Bichet, Delphine</creatorcontrib><creatorcontrib>Altafaj, Xavier</creatorcontrib><creatorcontrib>Weiss, Norbert</creatorcontrib><creatorcontrib>Ronjat, Michel</creatorcontrib><creatorcontrib>Dupuis, Alain</creatorcontrib><creatorcontrib>De Waard, Michel</creatorcontrib><title>Cavβ-subunit displacement is a key step to induce the reluctant state of P/Q calcium channels by direct G protein regulation</title><title>Proceedings of the National Academy of Sciences - PNAS</title><description>P/Q Ca 2+ channel activity is inhibited by G protein-coupled receptor activation. Channel inhibition requires a direct Gβγ binding onto the pore-forming subunit, Ca v 2.1. It is characterized by biophysical changes, including current amplitude reduction, activation kinetic slowing, and an I-V curve shift, which leads to a reluctant mode. Here, we have characterized the contribution of the auxiliary β 3 -subunit to channel regulation by G proteins. The shift in I-V to a P/Q reluctant mode is exclusively observed in the presence of β 3 . Along with the observation that Gβγ has no effect on the I-V curve of Ca v 2.1 alone, we propose that the reluctant mode promoted by Gβγ corresponds to a state in which the β 3 -subunit has been displaced from its channel-binding site. We validate this hypothesis with a β 3 -I-II 2.1 loop chimera construct. Gβγ binding onto the I-II 2.1 loop portion of the chimera releases the β 3 -binding domain and makes it available for binding onto the I-II loop of Ca v 1.2, a G protein-insensitive channel. This finding is extended to the full-length Ca v 2.1 channel by using fluorescence resonance energy transfer. Gβγ injection into Xenopus oocytes displaces a Cy3-labeled β 3 -subunit from a GFP-tagged Ca v 2.1 channel. We conclude that β-subunit dissociation from the channel complex constitutes a key step in P/Q calcium channel regulation by G proteins that underlies the reluctant state and is an important process for modulating neurotransmission through G protein-coupled receptors.</description><subject>Biological Sciences</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KxDAUhYMoOv6sXZqlm-pN07TNwoUM_oGggq5Lkt460UxamnRwFr6UD-IzGVAEN67u4n7fgXMIOWRwwqDip4NX4QQ4lDUUDNgGmTGQLCsLCZtkBpBXWV3kxQ7ZDeEFAKSoYZvsMAEVYxJm5H2uVp8fWZj05G2krQ2DUwaX6CO1gSr6imsaIg409tT6djJI4wLpiG4yUSUqRBWR9h29P32gRjljpyU1C-U9ukD1OmWOaCK9osPYR7Q-uc-TU9H2fp9sdcoFPPi5e-Tp8uJxfp3d3l3dzM9vs4FVMma8BFQaSuhYrqHNa5Q11FJw3olc1rrg2KXKTPCi7VqhhZS5RlGg0B0YofgeOfvOHSa9xNakdqNyzTDapRrXTa9s8_fj7aJ57lcNlyJNlvyjHz_t_aulwRtWNmVeVok4_p9ousm5iG-RfwG6w4cT</recordid><startdate>20040420</startdate><enddate>20040420</enddate><creator>Sandoz, Guillaume</creator><creator>Lopez-Gonzalez, Ignacio</creator><creator>Grunwald, Didier</creator><creator>Bichet, Delphine</creator><creator>Altafaj, Xavier</creator><creator>Weiss, Norbert</creator><creator>Ronjat, Michel</creator><creator>Dupuis, Alain</creator><creator>De Waard, Michel</creator><general>National Acad Sciences</general><general>National Academy of Sciences</general><scope>5PM</scope></search><sort><creationdate>20040420</creationdate><title>Cavβ-subunit displacement is a key step to induce the reluctant state of P/Q calcium channels by direct G protein regulation</title><author>Sandoz, Guillaume ; Lopez-Gonzalez, Ignacio ; Grunwald, Didier ; Bichet, Delphine ; Altafaj, Xavier ; Weiss, Norbert ; Ronjat, Michel ; Dupuis, Alain ; De Waard, Michel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p179t-360eab060f12b0d28e98089533f5298b43ef6491534dfd5b5992be54e5bf0c5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Biological Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sandoz, Guillaume</creatorcontrib><creatorcontrib>Lopez-Gonzalez, Ignacio</creatorcontrib><creatorcontrib>Grunwald, Didier</creatorcontrib><creatorcontrib>Bichet, Delphine</creatorcontrib><creatorcontrib>Altafaj, Xavier</creatorcontrib><creatorcontrib>Weiss, Norbert</creatorcontrib><creatorcontrib>Ronjat, Michel</creatorcontrib><creatorcontrib>Dupuis, Alain</creatorcontrib><creatorcontrib>De Waard, Michel</creatorcontrib><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sandoz, Guillaume</au><au>Lopez-Gonzalez, Ignacio</au><au>Grunwald, Didier</au><au>Bichet, Delphine</au><au>Altafaj, Xavier</au><au>Weiss, Norbert</au><au>Ronjat, Michel</au><au>Dupuis, Alain</au><au>De Waard, Michel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cavβ-subunit displacement is a key step to induce the reluctant state of P/Q calcium channels by direct G protein regulation</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><date>2004-04-20</date><risdate>2004</risdate><volume>101</volume><issue>16</issue><spage>6267</spage><epage>6272</epage><pages>6267-6272</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>P/Q Ca 2+ channel activity is inhibited by G protein-coupled receptor activation. Channel inhibition requires a direct Gβγ binding onto the pore-forming subunit, Ca v 2.1. It is characterized by biophysical changes, including current amplitude reduction, activation kinetic slowing, and an I-V curve shift, which leads to a reluctant mode. Here, we have characterized the contribution of the auxiliary β 3 -subunit to channel regulation by G proteins. The shift in I-V to a P/Q reluctant mode is exclusively observed in the presence of β 3 . Along with the observation that Gβγ has no effect on the I-V curve of Ca v 2.1 alone, we propose that the reluctant mode promoted by Gβγ corresponds to a state in which the β 3 -subunit has been displaced from its channel-binding site. We validate this hypothesis with a β 3 -I-II 2.1 loop chimera construct. Gβγ binding onto the I-II 2.1 loop portion of the chimera releases the β 3 -binding domain and makes it available for binding onto the I-II loop of Ca v 1.2, a G protein-insensitive channel. This finding is extended to the full-length Ca v 2.1 channel by using fluorescence resonance energy transfer. Gβγ injection into Xenopus oocytes displaces a Cy3-labeled β 3 -subunit from a GFP-tagged Ca v 2.1 channel. We conclude that β-subunit dissociation from the channel complex constitutes a key step in P/Q calcium channel regulation by G proteins that underlies the reluctant state and is an important process for modulating neurotransmission through G protein-coupled receptors.</abstract><pub>National Acad Sciences</pub><pmid>15071190</pmid><doi>10.1073/pnas.0306804101</doi><tpages>6</tpages></addata></record> |
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title | Cavβ-subunit displacement is a key step to induce the reluctant state of P/Q calcium channels by direct G protein regulation |
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