dc.creatorBarrantes, Francisco José
dc.date.accessioned2019-09-13T15:17:33Z
dc.date.accessioned2022-09-29T16:29:42Z
dc.date.available2019-09-13T15:17:33Z
dc.date.available2022-09-29T16:29:42Z
dc.date.created2019-09-13T15:17:33Z
dc.date.issued2015
dc.identifierBarrantes FJ. Phylogenetic conservation of protein–lipid motifs in pentameric ligand-gated ion channels. Biochimica et Biophysica Acta. 2015; 1848. https://doi.org/10.1016/j.bbamem.2015.03.028. Disponible en: https://repositorio.uca.edu.ar/handle/123456789/8736
dc.identifier0006-3002
dc.identifierhttps://repositorio.uca.edu.ar/handle/123456789/8736
dc.identifier10.1016/j.bbamem.2015.03.028
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3789401
dc.description.abstractAbstract: Using the crosstalk between the nicotinic acetylcholine receptor (nAChR) and its lipid microenvironment as a paradigm, this short overviewanalyzes the occurrence of structuralmotifswhich appear not only to be conserved within the nAChR family and contemporary eukaryotic members of the pentameric ligand-gated ion channel (pLGIC) superfamily, but also extend to prokaryotic homologues found in bacteria. The evolutionarily conserved design ismanifested in: 1) the concentric three-ring architecture of the transmembrane region, 2) the occurrence in this region of distinct lipid consensusmotifs in prokaryotic and eukaryotic pLGIC and 3) the key participation of the outer TM4 ring in conveying the influence of the lipidmembrane environment to themiddle TM1–TM3 ring and this, in turn, to the inner TM2 channel-lining ring, which determines the ion selectivity of the channel. The preservation of these constant structural–functional features throughout such a long phylogenetic span likely points to the successful gain-of-function conferred by their early acquisition. This article is part of a Special Issue entitled: Lipid–protein interactions.
dc.languageeng
dc.publisherElsevier B.V.
dc.rightshttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.rightsAcceso abierto
dc.sourceBiochimica et Biophysica Acta n° 1848, 2015
dc.subjectMEDICINA
dc.subjectRECEPTORES
dc.subjectPROTEINAS
dc.subjectLIPIDOS
dc.subjectCANALES IONICOS
dc.subjectCOLESTEROL
dc.titlePhylogenetic conservation of protein–lipid motifs in pentameric ligand-gated ion channels
dc.typeArtículos de revistas


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