Ion permeation through the gramicidin channel: Atomically detailed modeling by the stochastic difference equation

Atomically detailed descriptions of ionic solution, membrane, and the gramicidin channel are used to compute molecular dynamics trajectories of ion permeation. The microsecond trajectories are calculated with the Stochastic Difference Equation (SDE), which provides approximate solutions to the equat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Proteins, structure, function, and bioinformatics structure, function, and bioinformatics, 2003-01, Vol.50 (1), p.63-80
Hauptverfasser: Siva, Koneshan, Elber, Ron
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 80
container_issue 1
container_start_page 63
container_title Proteins, structure, function, and bioinformatics
container_volume 50
creator Siva, Koneshan
Elber, Ron
description Atomically detailed descriptions of ionic solution, membrane, and the gramicidin channel are used to compute molecular dynamics trajectories of ion permeation. The microsecond trajectories are calculated with the Stochastic Difference Equation (SDE), which provides approximate solutions to the equations of motions (with filtered high‐frequency modes) of extended timescales. The relative permeations of lithium, sodium, and potassium are estimated by using a novel, kinetic cycle protocol and are compared with experiment. The transport through native gramicidin and one fluoro‐valine variant is considered as well. Qualitative agreement between theory and experiment is obtained. The faster permeation rate of sodium compared to lithium is reproduced in the calculations. The calculations also reproduce the slower diffusion through a gramicidin with fluorinated valine compared to native gramicidin. The calculations are inconclusive about the relative rates of potassium and sodium. The experiment suggests that potassium permeates more quickly. We directly probe the kinetics of a biophysical process at a relevant time window without reducing the atomically detailed description of the system. The calculations were able to capture subtle balances between binding and diffusion that determine permeation rates. The same model gave the correct ordering of diffusion rates for cases in which electrostatic binding has opposite effects and must be supplemented by dynamic factors. Diffusion rates are faster when favorable electrostatic interactions of ions in the channel (compared to the solvent) are observed. Studies of a gramicidin variant suggest an opposite effect, in which permeation is faster for the less polar channel, indicating dynamic effects. Although both trends can be explained qualitatively, it is not possible to predict (before doing the SDE calculations) which factor is more important. Proteins 2003;50:63–80. © 2002 Wiley‐Liss, Inc.
doi_str_mv 10.1002/prot.10256
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_72885037</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>72885037</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3636-d6ca1a9982686353e31653b162539cf0fee876e6a2f6012b00c7686128c136f53</originalsourceid><addsrcrecordid>eNp9kE1vEzEQhi0Eomnhwg9APnFAWhjb9cdyqypaiqIWQRHcLMc7mxj2I7G9Kvn3uEmgt55mNHred6SHkFcM3jEA_n4dx1w2LtUTMmNQ6wqYOH1KZmCMroQ08ogcp_QLAFQt1HNyxPipZgpgRjZX40DXGHt0OZQ1r-I4LVdlIl1G1wcfmjBQv3LDgN0HepbHcnNdt6UNZhc6bGg_NtiFYUkX210u5bHwKQdPm9C2GHHwSHEz7V68IM9a1yV8eZgn5PvFx9vzT9X85vLq_GxeeaGEqhrlHXN1bbgySkiBgikpFkxxKWrfQototELleKuA8QWA14Vk3HgmVCvFCXmz7y16NhOmbPuQPHadG3CcktXcGAlCF_DtHvRxTClia9cx9C5uLQN7L9jeC7Y7wQV-fWidFj02D-jBaAHYHrgrbraPVNkvX29u_5VW-0xIGf_8z7j42yottLQ_ri_tN3398_NcgL0QfwEjqJY0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72885037</pqid></control><display><type>article</type><title>Ion permeation through the gramicidin channel: Atomically detailed modeling by the stochastic difference equation</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Siva, Koneshan ; Elber, Ron</creator><creatorcontrib>Siva, Koneshan ; Elber, Ron</creatorcontrib><description>Atomically detailed descriptions of ionic solution, membrane, and the gramicidin channel are used to compute molecular dynamics trajectories of ion permeation. The microsecond trajectories are calculated with the Stochastic Difference Equation (SDE), which provides approximate solutions to the equations of motions (with filtered high‐frequency modes) of extended timescales. The relative permeations of lithium, sodium, and potassium are estimated by using a novel, kinetic cycle protocol and are compared with experiment. The transport through native gramicidin and one fluoro‐valine variant is considered as well. Qualitative agreement between theory and experiment is obtained. The faster permeation rate of sodium compared to lithium is reproduced in the calculations. The calculations also reproduce the slower diffusion through a gramicidin with fluorinated valine compared to native gramicidin. The calculations are inconclusive about the relative rates of potassium and sodium. The experiment suggests that potassium permeates more quickly. We directly probe the kinetics of a biophysical process at a relevant time window without reducing the atomically detailed description of the system. The calculations were able to capture subtle balances between binding and diffusion that determine permeation rates. The same model gave the correct ordering of diffusion rates for cases in which electrostatic binding has opposite effects and must be supplemented by dynamic factors. Diffusion rates are faster when favorable electrostatic interactions of ions in the channel (compared to the solvent) are observed. Studies of a gramicidin variant suggest an opposite effect, in which permeation is faster for the less polar channel, indicating dynamic effects. Although both trends can be explained qualitatively, it is not possible to predict (before doing the SDE calculations) which factor is more important. Proteins 2003;50:63–80. © 2002 Wiley‐Liss, Inc.</description><identifier>ISSN: 0887-3585</identifier><identifier>EISSN: 1097-0134</identifier><identifier>DOI: 10.1002/prot.10256</identifier><identifier>PMID: 12471600</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Computational Biology - methods ; Computer Simulation ; computer simulations ; Diffusion ; functional optimization ; Gramicidin - chemistry ; Gramicidin - metabolism ; Ion Channels - chemistry ; Ion Channels - metabolism ; Ion Transport ; ionic solutions ; Kinetics ; Lithium - metabolism ; long time dynamics ; membranes ; Membranes - chemistry ; Models, Molecular ; Molecular Structure ; Motion ; Potassium - metabolism ; Sodium - metabolism ; Solvents - chemistry ; Static Electricity ; Stochastic Processes ; transport ; Valine - chemistry ; Water - chemistry</subject><ispartof>Proteins, structure, function, and bioinformatics, 2003-01, Vol.50 (1), p.63-80</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3636-d6ca1a9982686353e31653b162539cf0fee876e6a2f6012b00c7686128c136f53</citedby><cites>FETCH-LOGICAL-c3636-d6ca1a9982686353e31653b162539cf0fee876e6a2f6012b00c7686128c136f53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fprot.10256$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fprot.10256$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12471600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Siva, Koneshan</creatorcontrib><creatorcontrib>Elber, Ron</creatorcontrib><title>Ion permeation through the gramicidin channel: Atomically detailed modeling by the stochastic difference equation</title><title>Proteins, structure, function, and bioinformatics</title><addtitle>Proteins</addtitle><description>Atomically detailed descriptions of ionic solution, membrane, and the gramicidin channel are used to compute molecular dynamics trajectories of ion permeation. The microsecond trajectories are calculated with the Stochastic Difference Equation (SDE), which provides approximate solutions to the equations of motions (with filtered high‐frequency modes) of extended timescales. The relative permeations of lithium, sodium, and potassium are estimated by using a novel, kinetic cycle protocol and are compared with experiment. The transport through native gramicidin and one fluoro‐valine variant is considered as well. Qualitative agreement between theory and experiment is obtained. The faster permeation rate of sodium compared to lithium is reproduced in the calculations. The calculations also reproduce the slower diffusion through a gramicidin with fluorinated valine compared to native gramicidin. The calculations are inconclusive about the relative rates of potassium and sodium. The experiment suggests that potassium permeates more quickly. We directly probe the kinetics of a biophysical process at a relevant time window without reducing the atomically detailed description of the system. The calculations were able to capture subtle balances between binding and diffusion that determine permeation rates. The same model gave the correct ordering of diffusion rates for cases in which electrostatic binding has opposite effects and must be supplemented by dynamic factors. Diffusion rates are faster when favorable electrostatic interactions of ions in the channel (compared to the solvent) are observed. Studies of a gramicidin variant suggest an opposite effect, in which permeation is faster for the less polar channel, indicating dynamic effects. Although both trends can be explained qualitatively, it is not possible to predict (before doing the SDE calculations) which factor is more important. Proteins 2003;50:63–80. © 2002 Wiley‐Liss, Inc.</description><subject>Computational Biology - methods</subject><subject>Computer Simulation</subject><subject>computer simulations</subject><subject>Diffusion</subject><subject>functional optimization</subject><subject>Gramicidin - chemistry</subject><subject>Gramicidin - metabolism</subject><subject>Ion Channels - chemistry</subject><subject>Ion Channels - metabolism</subject><subject>Ion Transport</subject><subject>ionic solutions</subject><subject>Kinetics</subject><subject>Lithium - metabolism</subject><subject>long time dynamics</subject><subject>membranes</subject><subject>Membranes - chemistry</subject><subject>Models, Molecular</subject><subject>Molecular Structure</subject><subject>Motion</subject><subject>Potassium - metabolism</subject><subject>Sodium - metabolism</subject><subject>Solvents - chemistry</subject><subject>Static Electricity</subject><subject>Stochastic Processes</subject><subject>transport</subject><subject>Valine - chemistry</subject><subject>Water - chemistry</subject><issn>0887-3585</issn><issn>1097-0134</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1vEzEQhi0Eomnhwg9APnFAWhjb9cdyqypaiqIWQRHcLMc7mxj2I7G9Kvn3uEmgt55mNHred6SHkFcM3jEA_n4dx1w2LtUTMmNQ6wqYOH1KZmCMroQ08ogcp_QLAFQt1HNyxPipZgpgRjZX40DXGHt0OZQ1r-I4LVdlIl1G1wcfmjBQv3LDgN0HepbHcnNdt6UNZhc6bGg_NtiFYUkX210u5bHwKQdPm9C2GHHwSHEz7V68IM9a1yV8eZgn5PvFx9vzT9X85vLq_GxeeaGEqhrlHXN1bbgySkiBgikpFkxxKWrfQototELleKuA8QWA14Vk3HgmVCvFCXmz7y16NhOmbPuQPHadG3CcktXcGAlCF_DtHvRxTClia9cx9C5uLQN7L9jeC7Y7wQV-fWidFj02D-jBaAHYHrgrbraPVNkvX29u_5VW-0xIGf_8z7j42yottLQ_ri_tN3398_NcgL0QfwEjqJY0</recordid><startdate>20030101</startdate><enddate>20030101</enddate><creator>Siva, Koneshan</creator><creator>Elber, Ron</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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></search><sort><creationdate>20030101</creationdate><title>Ion permeation through the gramicidin channel: Atomically detailed modeling by the stochastic difference equation</title><author>Siva, Koneshan ; Elber, Ron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3636-d6ca1a9982686353e31653b162539cf0fee876e6a2f6012b00c7686128c136f53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Computational Biology - methods</topic><topic>Computer Simulation</topic><topic>computer simulations</topic><topic>Diffusion</topic><topic>functional optimization</topic><topic>Gramicidin - chemistry</topic><topic>Gramicidin - metabolism</topic><topic>Ion Channels - chemistry</topic><topic>Ion Channels - metabolism</topic><topic>Ion Transport</topic><topic>ionic solutions</topic><topic>Kinetics</topic><topic>Lithium - metabolism</topic><topic>long time dynamics</topic><topic>membranes</topic><topic>Membranes - chemistry</topic><topic>Models, Molecular</topic><topic>Molecular Structure</topic><topic>Motion</topic><topic>Potassium - metabolism</topic><topic>Sodium - metabolism</topic><topic>Solvents - chemistry</topic><topic>Static Electricity</topic><topic>Stochastic Processes</topic><topic>transport</topic><topic>Valine - chemistry</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Siva, Koneshan</creatorcontrib><creatorcontrib>Elber, Ron</creatorcontrib><collection>Istex</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><jtitle>Proteins, structure, function, and bioinformatics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Siva, Koneshan</au><au>Elber, Ron</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ion permeation through the gramicidin channel: Atomically detailed modeling by the stochastic difference equation</atitle><jtitle>Proteins, structure, function, and bioinformatics</jtitle><addtitle>Proteins</addtitle><date>2003-01-01</date><risdate>2003</risdate><volume>50</volume><issue>1</issue><spage>63</spage><epage>80</epage><pages>63-80</pages><issn>0887-3585</issn><eissn>1097-0134</eissn><abstract>Atomically detailed descriptions of ionic solution, membrane, and the gramicidin channel are used to compute molecular dynamics trajectories of ion permeation. The microsecond trajectories are calculated with the Stochastic Difference Equation (SDE), which provides approximate solutions to the equations of motions (with filtered high‐frequency modes) of extended timescales. The relative permeations of lithium, sodium, and potassium are estimated by using a novel, kinetic cycle protocol and are compared with experiment. The transport through native gramicidin and one fluoro‐valine variant is considered as well. Qualitative agreement between theory and experiment is obtained. The faster permeation rate of sodium compared to lithium is reproduced in the calculations. The calculations also reproduce the slower diffusion through a gramicidin with fluorinated valine compared to native gramicidin. The calculations are inconclusive about the relative rates of potassium and sodium. The experiment suggests that potassium permeates more quickly. We directly probe the kinetics of a biophysical process at a relevant time window without reducing the atomically detailed description of the system. The calculations were able to capture subtle balances between binding and diffusion that determine permeation rates. The same model gave the correct ordering of diffusion rates for cases in which electrostatic binding has opposite effects and must be supplemented by dynamic factors. Diffusion rates are faster when favorable electrostatic interactions of ions in the channel (compared to the solvent) are observed. Studies of a gramicidin variant suggest an opposite effect, in which permeation is faster for the less polar channel, indicating dynamic effects. Although both trends can be explained qualitatively, it is not possible to predict (before doing the SDE calculations) which factor is more important. Proteins 2003;50:63–80. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12471600</pmid><doi>10.1002/prot.10256</doi><tpages>18</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0887-3585
ispartof Proteins, structure, function, and bioinformatics, 2003-01, Vol.50 (1), p.63-80
issn 0887-3585
1097-0134
language eng
recordid cdi_proquest_miscellaneous_72885037
source MEDLINE; Access via Wiley Online Library
subjects Computational Biology - methods
Computer Simulation
computer simulations
Diffusion
functional optimization
Gramicidin - chemistry
Gramicidin - metabolism
Ion Channels - chemistry
Ion Channels - metabolism
Ion Transport
ionic solutions
Kinetics
Lithium - metabolism
long time dynamics
membranes
Membranes - chemistry
Models, Molecular
Molecular Structure
Motion
Potassium - metabolism
Sodium - metabolism
Solvents - chemistry
Static Electricity
Stochastic Processes
transport
Valine - chemistry
Water - chemistry
title Ion permeation through the gramicidin channel: Atomically detailed modeling by the stochastic difference equation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T23%3A56%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ion%20permeation%20through%20the%20gramicidin%20channel:%20Atomically%20detailed%20modeling%20by%20the%20stochastic%20difference%20equation&rft.jtitle=Proteins,%20structure,%20function,%20and%20bioinformatics&rft.au=Siva,%20Koneshan&rft.date=2003-01-01&rft.volume=50&rft.issue=1&rft.spage=63&rft.epage=80&rft.pages=63-80&rft.issn=0887-3585&rft.eissn=1097-0134&rft_id=info:doi/10.1002/prot.10256&rft_dat=%3Cproquest_cross%3E72885037%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=72885037&rft_id=info:pmid/12471600&rfr_iscdi=true