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Authordc.contributor.authorCerda, Oscar 
Authordc.contributor.authorCáceres, Mónica 
Authordc.contributor.authorPark, Kang Sik 
Authordc.contributor.authorLeiva Salcedo, Elías 
Authordc.contributor.authorRomero, Aníbal 
Authordc.contributor.authorVarela, Diego 
Authordc.contributor.authorTrimmer, James S. 
Authordc.contributor.authorStutzin Schottlander, Andrés 
Admission datedc.date.accessioned2019-03-18T11:53:07Z
Available datedc.date.available2019-03-18T11:53:07Z
Publication datedc.date.issued2015
Cita de ítemdc.identifier.citationPflugers Archiv European Journal of Physiology, Volumen 467, Issue 8, 2018, Pages 1723-1732
Identifierdc.identifier.issn14322013
Identifierdc.identifier.issn00316768
Identifierdc.identifier.other10.1007/s00424-014-1610-3
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/166602
Abstractdc.description.abstract© 2014, Springer-Verlag Berlin Heidelberg. Transient receptor potential melastatin-like 4 (TRPM4) is a Ca<sup>2+</sup>-activated non-selective cation channel expressed in a wide range of human tissues. TRPM4 participates in a variety of physiological processes such as T cell activation, myogenic vasoconstriction, and allergic reactions. TRPM4 Ca<sup>2+</sup> sensitivity is enhanced by calmodulin (CaM) and phosphathydilinositol 4, 5-bisphosphate (PI(4,5)P<inf>2</inf>) binding, as well as, under certain conditions, PKC activation. However, information as to the mechanisms of modulation of this channel remains unknown, including direct identification of phosphorylation sites on TRPM4 and their role in channel features. Here, we use mass-spectrometric-based proteomic approaches (immunoprecipitation and tandem mass spectrometry) to unambiguously identify S839 as a phosphorylation site present on human TRPM4 expressed in a human cell line. Site-directed mutagenesis employing a serine to alan
Lenguagedc.language.isoen
Publisherdc.publisherSpringer Verlag
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourcePflugers Archiv European Journal of Physiology
Keywordsdc.subjectBasolateral
Keywordsdc.subjectCasein kinase
Keywordsdc.subjectLC-MS/MS
Keywordsdc.subjectPhosphorylation
Keywordsdc.subjectTRP channels
Títulodc.titleCasein kinase-mediated phosphorylation of serine 839 is necessary for basolateral localization of the Ca
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile