Nanodomain Ca2+ of Ca2+ channels detected by a tethered genetically encoded Ca2+ sensor

被引:45
作者
Tay, Lai Hock [1 ]
Dick, Ivy E. [1 ]
Yang, Wanjun [1 ]
Mank, Marco [3 ]
Griesbeck, Oliver [3 ]
Yue, David T. [1 ,2 ]
机构
[1] Calcium Signals Lab, Dept Biomed Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[3] Max Planck Inst Neurobiol, AG Zellulare Dynam, D-82152 Martinsried, Germany
关键词
N-TYPE; ELEMENTARY MECHANISMS; TRANSMITTER RELEASE; CALCIUM CHANNELS; GATING-CURRENT; TROPONIN-C; CALMODULIN; FLUORESCENCE; DIFFUSION; FRET;
D O I
10.1038/ncomms1777
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Coupling of excitation to secretion, contraction and transcription often relies on Ca2+ computations within the nanodomain-a conceptual region extending tens of nanometers from the cytoplasmic mouth of Ca2+ channels. Theory predicts that nanodomain Ca2+ signals differ vastly from the slow submicromolar signals routinely observed in bulk cytoplasm. However, direct visualization of nanodomain Ca2+ far exceeds optical resolution of spatially distributed Ca2+ indicators. Here we couple an optical, genetically encoded Ca2+ indicator (TN-XL) to the carboxy tail of Ca(V)2.2 Ca2+ channels, enabling near-field imaging of the nanodomain. Under total internal reflection fluorescence microscopy, we detect Ca2+ responses indicative of large-amplitude pulses. Single-channel electrophysiology reveals a corresponding Ca2+ influx of only 0.085 pA, and fluorescence resonance energy transfer measurements estimate TN-XL distance to the cytoplasmic mouth at similar to 55 angstrom. Altogether, these findings raise the possibility that Ca2+ exits the channel through the analogue of molecular portals, mirroring the crystallographic images of side windows in voltage-gated K channels.
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页数:11
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共 60 条
[1]   ORL1 receptor-mediated internalization of N-type calcium channels [J].
Altier, C ;
Khosravani, H ;
Evans, RM ;
Hameed, S ;
Peloquin, JB ;
Vartian, BA ;
Chen, L ;
Beedle, AM ;
Ferguson, SSG ;
Mezghrani, A ;
Dubel, SJ ;
Bourinet, E ;
McRory, JE ;
Zamponi, GW .
NATURE NEUROSCIENCE, 2006, 9 (01) :31-40
[2]   Local calcium signaling in neurons [J].
Augustine, GJ ;
Santamaria, F ;
Tanaka, K .
NEURON, 2003, 40 (02) :331-346
[3]   TOTAL INTERNAL-REFLECTION FLUORESCENT MICROSCOPY [J].
AXELROD, D ;
THOMPSON, NL ;
BURGHARDT, TP .
JOURNAL OF MICROSCOPY-OXFORD, 1983, 129 (JAN) :19-28
[4]   Modulation of plasma membrane calcium-ATPase activity by local calcium microdomains near CRAC channels in human T cells [J].
Bautista, DM ;
Lewis, RS .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 556 (03) :805-817
[5]   BKCa-Cav channel complexes mediate rapid and localized Ca2+-activated K+ signaling [J].
Berkefeld, Henrike ;
Sailer, Claudia A. ;
Bildl, Wolfgang ;
Rohde, Volker ;
Thumfart, Joerg-Oliver ;
Eble, Silke ;
Klugbauer, Norbert ;
Reisinger, Ellen ;
Bischofberger, Josef ;
Oliver, Dominik ;
Knaus, Hans-Guenther ;
Schulte, Uwe ;
Fakler, Bernd .
SCIENCE, 2006, 314 (5799) :615-620
[6]   The versatility and universality of calcium signalling [J].
Berridge, MJ ;
Lipp, P ;
Bootman, MD .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2000, 1 (01) :11-21
[7]   MEASUREMENT OF CA-2+ CONCENTRATIONS IN LIVING CELLS [J].
BLINKS, JR ;
WIER, WG ;
HESS, P ;
PRENDERGAST, FG .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1982, 40 (1-2) :1-114
[8]   Detecting Rearrangements of Shaker and NaChBac in real-time with fluorescence spectroscopy in patch-clamped mammalian cells [J].
Blunck, R ;
Starace, DM ;
Correa, AM ;
Bezanilla, F .
BIOPHYSICAL JOURNAL, 2004, 86 (06) :3966-3980
[9]   Calcium current during a single action potential in a large presynaptic terminal of the rat brainstem [J].
Borst, JGG ;
Sakmann, B .
JOURNAL OF PHYSIOLOGY-LONDON, 1998, 506 (01) :143-157
[10]   NUCLEAR CA2+ CONCENTRATION MEASURED WITH SPECIFICALLY TARGETED RECOMBINANT AEQUORIN [J].
BRINI, M ;
MURGIA, M ;
PASTI, L ;
PICARD, D ;
POZZAN, T ;
RIZZUTO, R .
EMBO JOURNAL, 1993, 12 (12) :4813-4819