Por favor, use este identificador para citar o enlazar este ítem: https://repositorio.uca.edu.ar/handle/123456789/8736
Campo DC Valor Lengua/Idioma
dc.contributor.authorBarrantes, Francisco Josées
dc.date.accessioned2019-09-13T15:17:33Z-
dc.date.available2019-09-13T15:17:33Z-
dc.date.issued2015-
dc.identifier.citationBarrantes 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/123456789/8736es
dc.identifier.issn0006-3002-
dc.identifier.urihttps://repositorio.uca.edu.ar/handle/123456789/8736-
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.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherElsevier B.V.es
dc.rightsAcceso abierto*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.sourceBiochimica et Biophysica Acta n° 1848, 2015es
dc.subjectMEDICINAes
dc.subjectRECEPTORESes
dc.subjectPROTEINASes
dc.subjectLIPIDOSes
dc.subjectCANALES IONICOSes
dc.subjectCOLESTEROLes
dc.titlePhylogenetic conservation of protein–lipid motifs in pentameric ligand-gated ion channelses
dc.typeArtículoes
dc.identifier.doi10.1016/j.bbamem.2015.03.028-
uca.disciplinaMEDICINAes
uca.issnrd1es
uca.affiliationFil: Barrantes, Francisco José. Pontificia Universidad Católica Argentina. Facultad de Ciencias Médicas. Instituto de Investigaciones Biomédicas. Laboratorio de Neurobiología Molecular; Argentinaes
uca.affiliationFil: Barrantes, Francisco José. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes
uca.versionpublishedVersiones
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.languageiso639-1en-
crisitem.author.deptInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.deptLaboratorio de Neurobiología Molecular-
crisitem.author.deptFacultad de Ciencias Médicas-
crisitem.author.orcid0000-0002-4745-681X-
crisitem.author.parentorgFacultad de Ciencias Médicas-
crisitem.author.parentorgInstituto de Investigaciones Biomédicas - BIOMED-
crisitem.author.parentorgPontificia Universidad Católica Argentina-
Aparece en las colecciones: Artículos
Ficheros en este ítem:
Fichero Descripción Tamaño Formato
phylogenetic-conservation-protein-lipid.pdf1,3 MBAdobe PDFVista previa
Visualizar/Abrir
Mostrar el registro sencillo del ítem

Visualizaciones de página(s)

113
comprobado en 24-abr-2024

Descarga(s)

146
comprobado en 24-abr-2024

Google ScholarTM

Consultar


Altmetric


Este ítem está sujeto a una licencia Creative Commons Licencia Creative Commons Creative Commons