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dc.contributor.authorAivar, Paloma
dc.contributor.authorFernández-Orth, Juncal
dc.contributor.authorGomis Pérez, Carolina
dc.contributor.authorAlberdi González, Araitz
dc.contributor.authorAlaimo Campi, Alessandro ORCID
dc.contributor.authorRodríguez, Manuel S.
dc.contributor.authorGiraldez, Teresa
dc.contributor.authorMiranda, Pablo
dc.contributor.authorAreso Goiricelaya, María Pilar
dc.contributor.authorVillarroel Muñoz, Álvaro
dc.date.accessioned2014-02-13T17:28:06Z
dc.date.available2014-02-13T17:28:06Z
dc.date.issued2013-10-24
dc.identifier.citationPLoS ONE 10(7) : (2012) // e47263es
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10810/11470
dc.description12 p.es
dc.description.abstractKv7.2 and Kv7.3 are the main components of the neuronal voltage-dependent M-current, which is a subthreshold potassium conductance that exerts an important control on neuronal excitability. Despite their predominantly intracellular distribution, these channels must reach the plasma membrane in order to control neuronal activity. Thus, we analyzed the amino acid sequence of Kv7.2 to identify intrinsic signals that may control its surface expression. Removal of the interlinker connecting helix A and helix B of the intracellular C-terminus produces a large increase in the number of functional channels at the plasma membrane. Moreover, elimination of this linker increased the steady-state amount of protein, which was not associated with a decrease of protein degradation. The magnitude of this increase was inversely correlated with the number of helix A - helix B linkers present in the tetrameric channel assemblies. In contrast to the remarkable effect on the amount of Kv7.2 protein, removal of the Kv7.2 linker had no detectable impact on the steady-state levels of Kv7.3 protein.es
dc.description.sponsorshipThis work was supported by grants from the VII European framework program managed by the Fondo de Investigaciones Sanitarias (PI071316), from the Spanish Ministry of Education (BFU2009-07581 and SAF2006-1450), the Spanish Ion Channel Initiative Consolider project (CSD2008-00005), and the Basque Government (SAIOTEK SA-2006/00023). A. Alaimo was partially funded by Fundacion Biofisica Bizkaia. PA and JFO held a FPI fellowship from the Spanish Ministry of Science and Innovation (BES-2008-002314). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscriptes
dc.language.isoenges
dc.publisherPublic Library of Sciencees
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectC-terminuses
dc.subjectcalmodulines
dc.subjectcell membraneses
dc.subjectfluorescencees
dc.subjectfluorescence imaginges
dc.subjectintracellular membraneses
dc.subjectK+ channelses
dc.subjectKCNQ potassium channelses
dc.subjectKCNQ2/KCNQ3es
dc.subjectmembrane proteinses
dc.subjectpeptideses
dc.subjectpest sequenceses
dc.subjectprotein expressiones
dc.subjectpotein extractiones
dc.subjectribosomal tunneles
dc.subjecttraffickinges
dc.subjectxenopus oocyteses
dc.titleSurface Expression and Subunit Specific Control of Steady Protein Levels by the Kv7.2 Helix A-B Linkeres
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2012 Aivar et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es
dc.relation.publisherversionhttp://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0047263es
dc.identifier.doi10.1371/journal.pone.0047263
dc.departamentoesFarmacologíaes_ES
dc.departamentoeuFarmakologiaes_ES
dc.subject.categoriaAGRICULTURAL AND BIOLOGICAL SCIENCES
dc.subject.categoriaMEDICINE
dc.subject.categoriaBIOCHEMISTRY AND MOLECULAR BIOLOGY


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