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Originally published as Biophys J. BioFAST on March 16, 2007.
doi:10.1529/biophysj.106.102400
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Biophysical Journal 92:3901-3914 (2007)
© 2007 The Biophysical Society

On the Mechanism of TBA Block of the TRPV1 Channel

Andrés Jara Oseguera *, León D. Islas {dagger}, Refugio García-Villegas {ddagger} and Tamara Rosenbaum *

* Departamento de Biofísica, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México; {dagger} Departamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México; and {ddagger} Departamento de Fisiología, Biofísica y Neurociencias, Centro de Investigación y de Estudios Avanzados; México, D.F., México

Correspondence: Address correspondence to: Tamara Rosenbaum, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Apartado Postal 70-600. Circuito Exterior S/N; Ciudad Universitaria, C.P. 04510 México, D.F., México. Email: trosenba{at}ifc.unam.mx.

The transient receptor potential vanilloid 1 (TRPV1) channel is a nonselective cation channel activated by capsaicin and responsible for thermosensation. To date, little is known about the gating characteristics of these channels. Here we used tetrabutylammonium (TBA) to determine whether this molecule behaves as an ion conduction blocker in TRPV1 channels and to gain insight into the nature of the activation gate of this protein. TBA belongs to a family of classic potassium channel blockers that have been widely used as tools for determining the localization of the activation gate and the properties of the pore of several ion channels. We found TBA to be a voltage-dependent pore blocker and that the properties of block are consistent with an open-state blocker, with the TBA molecule binding to multiple open states, each with different blocker affinities. Kinetics of channel closure and burst-length analysis in the presence of blocker are consistent with a state-dependent blocking mechanism, with TBA interfering with closing of an activation gate. This activation gate may be located cytoplasmically with respect to the binding site of TBA ions, similar to what has been observed in potassium channels. We propose an allosteric model for TRPV1 activation and block by TBA, which explains our experimental data.




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[Abstract] [Full Text] [PDF]




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