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dc.creatorKasimova, MA
dc.creatorYazici, AT
dc.creatorYudin, Y
dc.creatorGranata, D
dc.creatorKlein, ML
dc.creatorRohacs, T
dc.creatorCarnevale, V
dc.date.accessioned2020-12-09T21:02:44Z
dc.date.available2020-12-09T21:02:44Z
dc.date.issued2018-11-01
dc.identifier.issn0022-1295
dc.identifier.issn1540-7748
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/4187
dc.identifier.other30333107 (pubmed)
dc.identifier.urihttp://hdl.handle.net/20.500.12613/4205
dc.description.abstract© 2018 Kasimova et al. The transient receptor potential channel vanilloid type 1 (TRPV1) is activated by a variety of endogenous and exogenous stimuli and is involved in nociception and body temperature regulation. Although the structure of TRPV1 has been experimentally determined in both the closed and open states, very little is known about its activation mechanism. In particular, the conformational changes that occur in the pore domain and result in ionic conduction have not yet been identified. Here we suggest a hypothetical molecular mechanism for TRPV1 activation, which involves rotation of a conserved asparagine in S6 from a position facing the S4-S5 linker toward the pore. This rotation is associated with hydration of the pore and dehydration of the four peripheral cavities located between each S6 and S4-S5 linker. In light of our hypothesis, we perform bioinformatics analyses of TRP and other evolutionary related ion channels, evaluate newly available structures, and reexamine previously reported water accessibility and mutagenesis experiments. These analyses provide several independent lines of evidence to support our hypothesis. Finally, we show that our proposed molecular mechanism is compatible with the prevailing theory that the selectivity filter acts as a secondary gate in TRPV1.
dc.format.extent1554-1566
dc.language.isoen
dc.relation.haspartJournal of General Physiology
dc.relation.isreferencedbyRockefeller University Press
dc.rightsCC BY-NC-SA
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectAsparagine
dc.subjectMolecular Dynamics Simulation
dc.subjectProtein Conformation
dc.subjectRotation
dc.subjectTRPV Cation Channels
dc.titleA hypothetical molecular mechanism for TRPV1 activation that invokes rotation of an S6 asparagine
dc.typeArticle
dc.type.genreJournal Article
dc.relation.doi10.1085/jgp.201812124
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.creator.orcidCarnevale, Vincenzo|0000-0002-0447-1278
dc.date.updated2020-12-09T21:02:39Z
refterms.dateFOA2020-12-09T21:02:45Z


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