Mechanism of allosteric modulation of rod cyclic nucleotide-gated channels
The cyclic nucleotide-gated (CNG) channel of retinal rod photoreceptor cells is an allosteric protein whose activation is coupled to a conformational change in the ligand-binding site. The bovine rod CNG channel can be activated by a number of different agonists, including cGMP, cIMP, and cAMP. Thes...
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Veröffentlicht in: | The Journal of general physiology 1999-05, Vol.113 (5), p.601-620 |
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description | The cyclic nucleotide-gated (CNG) channel of retinal rod photoreceptor cells is an allosteric protein whose activation is coupled to a conformational change in the ligand-binding site. The bovine rod CNG channel can be activated by a number of different agonists, including cGMP, cIMP, and cAMP. These agonists span three orders of magnitude in their equilibrium constants for the allosteric transition. We recorded single-channel currents at saturating cyclic nucleotide concentrations from the bovine rod CNG channel expressed in Xenopus oocytes as homomultimers of alpha subunits. The median open probability was 0.93 for cGMP, 0.47 for cIMP, and 0.01 for cAMP. The channels opened to a single conductance level of 26-30 pS at +80 mV. Using signal processing methods based on hidden Markov models, we determined that two closed and one open states are required to explain the gating at saturating ligand concentrations. We determined the maximum likelihood rate constants for two gating schemes containing two closed (denoted C) and one open (denoted O) states. For the C left and right arrow C left and right arrow O scheme, all rate constants were dependent on cyclic nucleotide. For the C left and right arrow O left and right arrow C scheme, the rate constants for only one of the transitions were cyclic nucleotide dependent. The opening rate constant was fastest for cGMP, intermediate for cIMP, and slowest for cAMP, while the closing rate constant was fastest for cAMP, intermediate for cIMP, and slowest for cGMP. We propose that interactions between the purine ring of the cyclic nucleotide and the binding domain are partially formed at the time of the transition state for the allosteric transition and serve to reduce the transition state energy and stabilize the activated conformation of the channel. When 1 microM Ni2+ was applied in addition to cyclic nucleotide, the open time increased markedly, and the closed time decreased slightly. The interactions between H420 and Ni2+ occur primarily after the transition state for the allosteric transition. |
doi_str_mv | 10.1085/jgp.113.5.601 |
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The bovine rod CNG channel can be activated by a number of different agonists, including cGMP, cIMP, and cAMP. These agonists span three orders of magnitude in their equilibrium constants for the allosteric transition. We recorded single-channel currents at saturating cyclic nucleotide concentrations from the bovine rod CNG channel expressed in Xenopus oocytes as homomultimers of alpha subunits. The median open probability was 0.93 for cGMP, 0.47 for cIMP, and 0.01 for cAMP. The channels opened to a single conductance level of 26-30 pS at +80 mV. Using signal processing methods based on hidden Markov models, we determined that two closed and one open states are required to explain the gating at saturating ligand concentrations. We determined the maximum likelihood rate constants for two gating schemes containing two closed (denoted C) and one open (denoted O) states. For the C left and right arrow C left and right arrow O scheme, all rate constants were dependent on cyclic nucleotide. For the C left and right arrow O left and right arrow C scheme, the rate constants for only one of the transitions were cyclic nucleotide dependent. The opening rate constant was fastest for cGMP, intermediate for cIMP, and slowest for cAMP, while the closing rate constant was fastest for cAMP, intermediate for cIMP, and slowest for cGMP. We propose that interactions between the purine ring of the cyclic nucleotide and the binding domain are partially formed at the time of the transition state for the allosteric transition and serve to reduce the transition state energy and stabilize the activated conformation of the channel. When 1 microM Ni2+ was applied in addition to cyclic nucleotide, the open time increased markedly, and the closed time decreased slightly. The interactions between H420 and Ni2+ occur primarily after the transition state for the allosteric transition.</description><identifier>ISSN: 0022-1295</identifier><identifier>EISSN: 1540-7748</identifier><identifier>DOI: 10.1085/jgp.113.5.601</identifier><identifier>PMID: 10228178</identifier><identifier>CODEN: JGPLAD</identifier><language>eng</language><publisher>United States: Rockefeller University Press</publisher><subject>Algorithms ; Anatomy & physiology ; Animals ; Binding Sites ; Cattle ; Cyclic AMP - physiology ; Cyclic GMP - physiology ; Cyclic IMP - physiology ; Cyclic Nucleotide-Gated Cation Channels ; Electric Stimulation ; Ion Channel Gating - physiology ; Ion Channels - physiology ; Ions ; Kinetics ; Ligands ; Markov Chains ; Models, Biological ; Nickel - pharmacology ; Patch-Clamp Techniques ; Protein Conformation ; Proteins ; Retinal Rod Photoreceptor Cells - physiology ; Xenopus laevis</subject><ispartof>The Journal of general physiology, 1999-05, Vol.113 (5), p.601-620</ispartof><rights>Copyright Rockefeller University Press May 1999</rights><rights>1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-9271acef878b52b57b714aab321bf2f1c46a01760a74dcd9ade506bde3782bc83</citedby><cites>FETCH-LOGICAL-c410t-9271acef878b52b57b714aab321bf2f1c46a01760a74dcd9ade506bde3782bc83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10228178$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sunderman, E R</creatorcontrib><creatorcontrib>Zagotta, W N</creatorcontrib><title>Mechanism of allosteric modulation of rod cyclic nucleotide-gated channels</title><title>The Journal of general physiology</title><addtitle>J Gen Physiol</addtitle><description>The cyclic nucleotide-gated (CNG) channel of retinal rod photoreceptor cells is an allosteric protein whose activation is coupled to a conformational change in the ligand-binding site. The bovine rod CNG channel can be activated by a number of different agonists, including cGMP, cIMP, and cAMP. These agonists span three orders of magnitude in their equilibrium constants for the allosteric transition. We recorded single-channel currents at saturating cyclic nucleotide concentrations from the bovine rod CNG channel expressed in Xenopus oocytes as homomultimers of alpha subunits. The median open probability was 0.93 for cGMP, 0.47 for cIMP, and 0.01 for cAMP. The channels opened to a single conductance level of 26-30 pS at +80 mV. Using signal processing methods based on hidden Markov models, we determined that two closed and one open states are required to explain the gating at saturating ligand concentrations. We determined the maximum likelihood rate constants for two gating schemes containing two closed (denoted C) and one open (denoted O) states. For the C left and right arrow C left and right arrow O scheme, all rate constants were dependent on cyclic nucleotide. For the C left and right arrow O left and right arrow C scheme, the rate constants for only one of the transitions were cyclic nucleotide dependent. The opening rate constant was fastest for cGMP, intermediate for cIMP, and slowest for cAMP, while the closing rate constant was fastest for cAMP, intermediate for cIMP, and slowest for cGMP. We propose that interactions between the purine ring of the cyclic nucleotide and the binding domain are partially formed at the time of the transition state for the allosteric transition and serve to reduce the transition state energy and stabilize the activated conformation of the channel. When 1 microM Ni2+ was applied in addition to cyclic nucleotide, the open time increased markedly, and the closed time decreased slightly. The interactions between H420 and Ni2+ occur primarily after the transition state for the allosteric transition.</description><subject>Algorithms</subject><subject>Anatomy & physiology</subject><subject>Animals</subject><subject>Binding Sites</subject><subject>Cattle</subject><subject>Cyclic AMP - physiology</subject><subject>Cyclic GMP - physiology</subject><subject>Cyclic IMP - physiology</subject><subject>Cyclic Nucleotide-Gated Cation Channels</subject><subject>Electric Stimulation</subject><subject>Ion Channel Gating - physiology</subject><subject>Ion Channels - physiology</subject><subject>Ions</subject><subject>Kinetics</subject><subject>Ligands</subject><subject>Markov Chains</subject><subject>Models, Biological</subject><subject>Nickel - pharmacology</subject><subject>Patch-Clamp Techniques</subject><subject>Protein Conformation</subject><subject>Proteins</subject><subject>Retinal Rod Photoreceptor Cells - physiology</subject><subject>Xenopus laevis</subject><issn>0022-1295</issn><issn>1540-7748</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkb1PwzAQxS0EouVjZEURA1uKz4ljZ0FCFZ8qYoHZcmynTeXExU6Q-t_j0goVbjnJ7-enu3sIXQCeAOb0ZjlfTQCyCZ0UGA7QGGiOU8ZyfojGGBOSAinpCJ2EsMSxKMHHaARR4MD4GL28GrWQXRPaxNWJtNaF3vhGJa3Tg5V947qN4J1O1FrZKHSDssb1jTbpXPYmvsf_nbHhDB3V0gZzvuun6OPh_n36lM7eHp-nd7NU5YD7tCQMpDI1Z7yipKKsYpBLWWUEqprUoPJCYmAFlizXSpdSG4qLSpuMcVIpnp2i263vaqhao5Xpei-tWPmmlX4tnGzEX6VrFmLuvgSJVQKJBtc7A-8-BxN60TZBGWtlZ9wQRFGyDPIf8OofuHSD7-JygmAK8ZY4i1C6hZR3IXhT_04CWGwiEjEiESMSVMSIIn-5P_4evc0k-wYrh44S</recordid><startdate>199905</startdate><enddate>199905</enddate><creator>Sunderman, E R</creator><creator>Zagotta, W N</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</general><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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>199905</creationdate><title>Mechanism of allosteric modulation of rod cyclic nucleotide-gated channels</title><author>Sunderman, E R ; Zagotta, W N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-9271acef878b52b57b714aab321bf2f1c46a01760a74dcd9ade506bde3782bc83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Algorithms</topic><topic>Anatomy & physiology</topic><topic>Animals</topic><topic>Binding Sites</topic><topic>Cattle</topic><topic>Cyclic AMP - physiology</topic><topic>Cyclic GMP - physiology</topic><topic>Cyclic IMP - physiology</topic><topic>Cyclic Nucleotide-Gated Cation Channels</topic><topic>Electric Stimulation</topic><topic>Ion Channel Gating - physiology</topic><topic>Ion Channels - physiology</topic><topic>Ions</topic><topic>Kinetics</topic><topic>Ligands</topic><topic>Markov Chains</topic><topic>Models, Biological</topic><topic>Nickel - pharmacology</topic><topic>Patch-Clamp Techniques</topic><topic>Protein Conformation</topic><topic>Proteins</topic><topic>Retinal Rod Photoreceptor Cells - physiology</topic><topic>Xenopus laevis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sunderman, E R</creatorcontrib><creatorcontrib>Zagotta, W N</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of general physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sunderman, E R</au><au>Zagotta, W N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mechanism of allosteric modulation of rod cyclic nucleotide-gated channels</atitle><jtitle>The Journal of general physiology</jtitle><addtitle>J Gen Physiol</addtitle><date>1999-05</date><risdate>1999</risdate><volume>113</volume><issue>5</issue><spage>601</spage><epage>620</epage><pages>601-620</pages><issn>0022-1295</issn><eissn>1540-7748</eissn><coden>JGPLAD</coden><abstract>The cyclic nucleotide-gated (CNG) channel of retinal rod photoreceptor cells is an allosteric protein whose activation is coupled to a conformational change in the ligand-binding site. The bovine rod CNG channel can be activated by a number of different agonists, including cGMP, cIMP, and cAMP. These agonists span three orders of magnitude in their equilibrium constants for the allosteric transition. We recorded single-channel currents at saturating cyclic nucleotide concentrations from the bovine rod CNG channel expressed in Xenopus oocytes as homomultimers of alpha subunits. The median open probability was 0.93 for cGMP, 0.47 for cIMP, and 0.01 for cAMP. The channels opened to a single conductance level of 26-30 pS at +80 mV. Using signal processing methods based on hidden Markov models, we determined that two closed and one open states are required to explain the gating at saturating ligand concentrations. We determined the maximum likelihood rate constants for two gating schemes containing two closed (denoted C) and one open (denoted O) states. For the C left and right arrow C left and right arrow O scheme, all rate constants were dependent on cyclic nucleotide. For the C left and right arrow O left and right arrow C scheme, the rate constants for only one of the transitions were cyclic nucleotide dependent. The opening rate constant was fastest for cGMP, intermediate for cIMP, and slowest for cAMP, while the closing rate constant was fastest for cAMP, intermediate for cIMP, and slowest for cGMP. We propose that interactions between the purine ring of the cyclic nucleotide and the binding domain are partially formed at the time of the transition state for the allosteric transition and serve to reduce the transition state energy and stabilize the activated conformation of the channel. When 1 microM Ni2+ was applied in addition to cyclic nucleotide, the open time increased markedly, and the closed time decreased slightly. 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subjects | Algorithms Anatomy & physiology Animals Binding Sites Cattle Cyclic AMP - physiology Cyclic GMP - physiology Cyclic IMP - physiology Cyclic Nucleotide-Gated Cation Channels Electric Stimulation Ion Channel Gating - physiology Ion Channels - physiology Ions Kinetics Ligands Markov Chains Models, Biological Nickel - pharmacology Patch-Clamp Techniques Protein Conformation Proteins Retinal Rod Photoreceptor Cells - physiology Xenopus laevis |
title | Mechanism of allosteric modulation of rod cyclic nucleotide-gated channels |
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