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dc.contributor.authorValente, Pierluigi-
dc.contributor.authorGarcía-Sanz, Nuria-
dc.contributor.authorGomis, Ana-
dc.contributor.authorFernández-Carvajal, Asia-
dc.contributor.authorFernández-Ballester, Gregorio-
dc.contributor.authorViana, Félix-
dc.contributor.authorBelmonte, Carlos-
dc.contributor.authorFerrer-Montiel, Antonio-
dc.date.accessioned2012-12-14T12:37:33Z-
dc.date.available2012-12-14T12:37:33Z-
dc.date.issued2008-
dc.identifierdoi: 10.1096/fj.08-107425-
dc.identifierissn: 0892-6638-
dc.identifiere-issn: 1530-6860-
dc.identifier.citationFASEB Journal 2289): 3298-3309 (2008)-
dc.identifier.urihttp://hdl.handle.net/10261/62974-
dc.description.abstractTransient receptor potential vanilloid receptor subtype I (TRPV1) is an ion channel gated by physical and chemical stimuli that belongs to the TRPV protein family. TRPV receptors contain a highly conserved, 6-mer segment near the channel gate, known as the TRP box, whose function remains unknown. Here, we performed an alanine scanning mutagenesis of the TRP box of TRPV1 (IWKLQR) and found that mutation of this motif affected channel gating by raising the free energy of channel activation. Functional characterization of TRPV1 mutants showed that substitution of I696, W697, and R701 by alanine severely affected voltage- and heat-dependent activation and notably reduced the capsaicin responsiveness and tachyphylaxia, while mutation of K698, L699, and Q700 had minor effects. In addition, mutation of I696 to alanine promoted a strong outward rectification at negative membrane potentials, and slowed the kinetics of channel activation. Taken together, our findings suggest that modification of I696, W697, and R701 to alanine altered channel function by affecting events downstream of the initial stimuli-sensing step and imply that inter-subunit interactions within the TRP box play an important role in TRPV1 gating. © FASEB.-
dc.description.sponsorshipThis work was supported by grants from the Spanish Ministry of Education and Science (MEC) (SAF2006–2580 to A.F.-M. and BFU2005–03986 to A.G.), the Fundación Ramón Areces (to A.F.-M), and the Generalitat Valenciana (GV-ACOMP06/202 to A.F-M. and GV05/076 to A.G.).-
dc.language.isoeng-
dc.publisherFederation of American Societies for Experimental Biology-
dc.rightsopenAccess-
dc.titleIdentification of molecular determinants of channel gating in the transient receptor potential box of vanilloid receptor I-
dc.typeartículo-
dc.identifier.doi10.1096/fj.08-107425-
dc.date.updated2012-12-14T12:37:33Z-
dc.description.versionPeer Reviewed-
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