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Nanodomain Ca(2+) of Ca(2+) channels detected by a tethered genetically encoded Ca(2+) sensor

Coupling of excitation to secretion, contraction, and transcription often relies upon Ca(2+) computations within the nanodomain—a conceptual region extending tens of nanometers from the cytoplasmic mouth of Ca(2+) channels. Theory predicts that nanodomain Ca(2+) signals differ vastly from the slow s...

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Detalles Bibliográficos
Autores principales: Tay, Lai Hock, Dick, Ivy E., Yang, Wanjun, Mank, Marco, Griesbeck, Oliver, Yue, David T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3615648/
https://www.ncbi.nlm.nih.gov/pubmed/22491326
http://dx.doi.org/10.1038/ncomms1777
Descripción
Sumario:Coupling of excitation to secretion, contraction, and transcription often relies upon Ca(2+) computations within the nanodomain—a conceptual region extending tens of nanometers from the cytoplasmic mouth of Ca(2+) channels. Theory predicts that nanodomain Ca(2+) signals differ vastly from the slow submicromolar signals routinely observed in bulk cytoplasm. However, direct visualization of nanodomain Ca(2+) far exceeds optical resolution of spatially distributed Ca(2+) indicators. Here we couple an optical genetically encoded Ca(2+) indicator (TN-XL) to the carboxyl tail of Ca(V)2.2 Ca(2+) channels, enabling nearfield imaging of the nanodomain. Under TIRF microscopy, we detect Ca(2+) responses indicative of large-amplitude pulses. Single-channel electrophysiology reveals a corresponding Ca(2+) influx of only 0.085 pA, and FRET measurements estimate TN-XL distance to the cytoplasmic mouth at ~55 Å. Altogether, these findings raise the possibility that Ca(2+) exits the channel through the analog of molecular portals, mirroring the crystallographic images of side windows in voltage-gated K channels.