The quality of maximum likelihood estimates of ion channel rate constants
Properties of maximum likelihood estimators of rate constants for channel mechanisms are investigated, to see what can and cannot be inferred from experimental results. The implementation of the HJCFIT method is described; it maximises the likelihood of an entire sequence of apparent open and shut t...
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creator | Colquhoun, D Hatton, C J Hawkes, A G |
description | Properties of maximum likelihood estimators of rate constants for channel mechanisms are investigated, to see what can and
cannot be inferred from experimental results. The implementation of the HJCFIT method is described; it maximises the likelihood
of an entire sequence of apparent open and shut times, with the rate constants in a specified reaction mechanism as free parameters.
The exact method for missed brief events is used. Several methods for testing the quality of the fit are described. The distributions
of rate constants, and correlations between them, are investigated by doing sets of 1000 fits to simulated experiments. In
a standard nicotinic receptor mechanism, all nine free rate constants can be estimated even from one single channel recording,
as long as the two binding sites are independent, even when the number of channels in the patch is not known. The estimates
of rate constants that apply to diliganded channels are robust; good estimates can be obtained even with erroneous assumptions
(e.g. about the value of a fixed rate constant or the independence of sites). Rate constants that require distinction between
the two sites are less robust, and require that an EC 50 be specified, or that records at two concentrations be fitted simultaneously. Despite the complexity of the problem, it appears
that there exist two solutions with very similar likelihoods, as in the simplest case. The hazards that result from this,
and from the strong positive correlation between estimates of opening and shutting rates, are discussed. |
doi_str_mv | 10.1113/jphysiol.2002.034165 |
format | Article |
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cannot be inferred from experimental results. The implementation of the HJCFIT method is described; it maximises the likelihood
of an entire sequence of apparent open and shut times, with the rate constants in a specified reaction mechanism as free parameters.
The exact method for missed brief events is used. Several methods for testing the quality of the fit are described. The distributions
of rate constants, and correlations between them, are investigated by doing sets of 1000 fits to simulated experiments. In
a standard nicotinic receptor mechanism, all nine free rate constants can be estimated even from one single channel recording,
as long as the two binding sites are independent, even when the number of channels in the patch is not known. The estimates
of rate constants that apply to diliganded channels are robust; good estimates can be obtained even with erroneous assumptions
(e.g. about the value of a fixed rate constant or the independence of sites). Rate constants that require distinction between
the two sites are less robust, and require that an EC 50 be specified, or that records at two concentrations be fitted simultaneously. Despite the complexity of the problem, it appears
that there exist two solutions with very similar likelihoods, as in the simplest case. The hazards that result from this,
and from the strong positive correlation between estimates of opening and shutting rates, are discussed.</description><identifier>ISSN: 0022-3751</identifier><identifier>EISSN: 1469-7793</identifier><identifier>DOI: 10.1113/jphysiol.2002.034165</identifier><identifier>PMID: 12562901</identifier><language>eng</language><publisher>England: The Physiological Society</publisher><subject>Binding Sites - physiology ; Computer Simulation ; Ion Channel Gating - physiology ; Ligands ; Models, Biological ; Receptors, Cholinergic - physiology ; Research Papers ; Software</subject><ispartof>The Journal of physiology, 2003-03, Vol.547 (3), p.699-728</ispartof><rights>The Physiological Society 2003 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-3c7677fcb102b2af0ef2bcc7f2b0b8c8d183d98ed8dff90d491a694781cf6bdb3</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/PMC2342730/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2342730/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12562901$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Colquhoun, D</creatorcontrib><creatorcontrib>Hatton, C J</creatorcontrib><creatorcontrib>Hawkes, A G</creatorcontrib><title>The quality of maximum likelihood estimates of ion channel rate constants</title><title>The Journal of physiology</title><addtitle>J Physiol</addtitle><description>Properties of maximum likelihood estimators of rate constants for channel mechanisms are investigated, to see what can and
cannot be inferred from experimental results. The implementation of the HJCFIT method is described; it maximises the likelihood
of an entire sequence of apparent open and shut times, with the rate constants in a specified reaction mechanism as free parameters.
The exact method for missed brief events is used. Several methods for testing the quality of the fit are described. The distributions
of rate constants, and correlations between them, are investigated by doing sets of 1000 fits to simulated experiments. In
a standard nicotinic receptor mechanism, all nine free rate constants can be estimated even from one single channel recording,
as long as the two binding sites are independent, even when the number of channels in the patch is not known. The estimates
of rate constants that apply to diliganded channels are robust; good estimates can be obtained even with erroneous assumptions
(e.g. about the value of a fixed rate constant or the independence of sites). Rate constants that require distinction between
the two sites are less robust, and require that an EC 50 be specified, or that records at two concentrations be fitted simultaneously. Despite the complexity of the problem, it appears
that there exist two solutions with very similar likelihoods, as in the simplest case. The hazards that result from this,
and from the strong positive correlation between estimates of opening and shutting rates, are discussed.</description><subject>Binding Sites - physiology</subject><subject>Computer Simulation</subject><subject>Ion Channel Gating - physiology</subject><subject>Ligands</subject><subject>Models, Biological</subject><subject>Receptors, Cholinergic - physiology</subject><subject>Research Papers</subject><subject>Software</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUclOwzAQtRAIyvIHCOUEpxSPncbxBQlVLJWQuMDZchy7MThxiROgf4-rlO0yI81782Z5CJ0CngIAvXxZ1etgvZsSjMkU0wzy2Q6aQJbzlDFOd9EkAiSlbAYH6DCEF4yBYs730QGQWU44hglaPNU6eRuks_068SZp5KdthiZx9lU7W3tfJTr0tpG9Dhvc-jZRtWxb7ZIuFhPl29DLtg_HaM9IF_TJNh-h59ubp_l9-vB4t5hfP6Qqo3mfUsVyxowqAZOSSIO1IaVSLEZcFqqooKAVL3RVVMZwXGUcZM4zVoAyeVmV9AhdjbqroWx0pXTbd9KJVReX7NbCSyv-I62txdK_C0IzwiiOAudbgc6_DfE60digtHOy1X4IglEAFr8WidlIVJ0PodPmZwhgsfFAfHsgNh6I0YPYdvZ3wd-m7dMj4WIk1HZZf9hOi1EmeGV1vxazjAkqcs7pFy1rle8</recordid><startdate>20030315</startdate><enddate>20030315</enddate><creator>Colquhoun, D</creator><creator>Hatton, C J</creator><creator>Hawkes, A G</creator><general>The Physiological Society</general><general>Blackwell Science Inc</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030315</creationdate><title>The quality of maximum likelihood estimates of ion channel rate constants</title><author>Colquhoun, D ; Hatton, C J ; Hawkes, A G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-3c7677fcb102b2af0ef2bcc7f2b0b8c8d183d98ed8dff90d491a694781cf6bdb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Binding Sites - physiology</topic><topic>Computer Simulation</topic><topic>Ion Channel Gating - physiology</topic><topic>Ligands</topic><topic>Models, Biological</topic><topic>Receptors, Cholinergic - physiology</topic><topic>Research Papers</topic><topic>Software</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Colquhoun, D</creatorcontrib><creatorcontrib>Hatton, C J</creatorcontrib><creatorcontrib>Hawkes, A G</creatorcontrib><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 physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Colquhoun, D</au><au>Hatton, C J</au><au>Hawkes, A G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The quality of maximum likelihood estimates of ion channel rate constants</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2003-03-15</date><risdate>2003</risdate><volume>547</volume><issue>3</issue><spage>699</spage><epage>728</epage><pages>699-728</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>Properties of maximum likelihood estimators of rate constants for channel mechanisms are investigated, to see what can and
cannot be inferred from experimental results. The implementation of the HJCFIT method is described; it maximises the likelihood
of an entire sequence of apparent open and shut times, with the rate constants in a specified reaction mechanism as free parameters.
The exact method for missed brief events is used. Several methods for testing the quality of the fit are described. The distributions
of rate constants, and correlations between them, are investigated by doing sets of 1000 fits to simulated experiments. In
a standard nicotinic receptor mechanism, all nine free rate constants can be estimated even from one single channel recording,
as long as the two binding sites are independent, even when the number of channels in the patch is not known. The estimates
of rate constants that apply to diliganded channels are robust; good estimates can be obtained even with erroneous assumptions
(e.g. about the value of a fixed rate constant or the independence of sites). Rate constants that require distinction between
the two sites are less robust, and require that an EC 50 be specified, or that records at two concentrations be fitted simultaneously. Despite the complexity of the problem, it appears
that there exist two solutions with very similar likelihoods, as in the simplest case. The hazards that result from this,
and from the strong positive correlation between estimates of opening and shutting rates, are discussed.</abstract><cop>England</cop><pub>The Physiological Society</pub><pmid>12562901</pmid><doi>10.1113/jphysiol.2002.034165</doi><tpages>30</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Binding Sites - physiology Computer Simulation Ion Channel Gating - physiology Ligands Models, Biological Receptors, Cholinergic - physiology Research Papers Software |
title | The quality of maximum likelihood estimates of ion channel rate constants |
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