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Brownian dynamics investigation into the conductance state of the MscS channel crystal structure

Vora, Taira; Corry, Ben; Chung, Shin-Ho

Description

We suggest that the crystal structure of the mechanosensitive channel of small conductance is in a minimally conductive state rather than being fully activated. Performing Brownian dynamics simulations on the crystal structure show that no ions pass through it. When simulations are conducted on just the transmembrane domain (excluding the cytoplasmic residues 128 to 280) ions are seen to pass through the channel, but the conductance of ∼ 30 pS is well below experimentally measured values. The...[Show more]

dc.contributor.authorVora, Taira
dc.contributor.authorCorry, Ben
dc.contributor.authorChung, Shin-Ho
dc.date.accessioned2015-12-08T22:40:09Z
dc.identifier.issn0006-3002
dc.identifier.urihttp://hdl.handle.net/1885/36378
dc.description.abstractWe suggest that the crystal structure of the mechanosensitive channel of small conductance is in a minimally conductive state rather than being fully activated. Performing Brownian dynamics simulations on the crystal structure show that no ions pass through it. When simulations are conducted on just the transmembrane domain (excluding the cytoplasmic residues 128 to 280) ions are seen to pass through the channel, but the conductance of ∼ 30 pS is well below experimentally measured values. The mutation L109S that replaces a pore lining hydrophobic residue with a polar one is found to have little effect on the conductance of the channel. Widening the hydrophobic region of the pore by 2.5 Å however, increases the channel conductance to over 200 pS suggesting that only a minimal conformational change is required to gate the pore.
dc.publisherElsevier
dc.sourceBiochimica et Biophysica Acta: International journal of Biochemistry and Biophysics
dc.subjectKeywords: ion channel; mechanosensitive ion channel; unclassified drug; article; conformational transition; crystal structure; gene mutation; hydrophobicity; ion conductance; ion transport; molecular dynamics; porosity; priority journal; protein conformation; simul Brownian dynamic; Conductance; Electrostatic; Ion channel; Mechanosensation; MscS
dc.titleBrownian dynamics investigation into the conductance state of the MscS channel crystal structure
dc.typeJournal article
local.description.notesImported from ARIES
local.identifier.citationvolume1758
dc.date.issued2006
local.identifier.absfor060104 - Cell Metabolism
local.identifier.ariespublicationu9204316xPUB135
local.type.statusPublished Version
local.contributor.affiliationVora, Taira, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationCorry, Ben, University of Western Australia
local.contributor.affiliationChung, Shin-Ho, College of Medicine, Biology and Environment, ANU
local.description.embargo2037-12-31
local.bibliographicCitation.startpage730
local.bibliographicCitation.lastpage737
local.identifier.doi10.1016/j.bbamem.2006.04.014
dc.date.updated2015-12-08T10:21:31Z
local.identifier.scopusID2-s2.0-33746066773
CollectionsANU Research Publications

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