Imaging single-channel calcium microdomains by total internal reflection microscopy
The microdomains of Ca2+ in the cytosol around the mouth of open Ca2+ channels are the basic `building blocks' from which cellular Ca2+ signals are constructed. Moreover, the kinetics of local [Ca2+] closely reflect channel gating, so their measurement holds promise as an alternative to electro...
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Sociedad de Biología de Chile
2004
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oai:scielo:S0716-976020040004000252005-06-02Imaging single-channel calcium microdomains by total internal reflection microscopyDEMURO,ANGELOPARKER,IAN single-channel recording calcium imaging TIRFM N-type Ca2+ channels The microdomains of Ca2+ in the cytosol around the mouth of open Ca2+ channels are the basic `building blocks' from which cellular Ca2+ signals are constructed. Moreover, the kinetics of local [Ca2+] closely reflect channel gating, so their measurement holds promise as an alternative to electrophysiological patch-clamp recording as a means to study single channel behavior. We have thus explored the development of optical techniques capable of imaging single-channel Ca2+ signals with good spatial and temporal resolution, and describe results obtained using total internal reflection fluorescence microscopy to monitor Ca2+ influx through single N-type channels expressed in Xenopus oocytesinfo:eu-repo/semantics/openAccessSociedad de Biología de ChileBiological Research v.37 n.4 20042004-01-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000400025en10.4067/S0716-97602004000400025 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
English |
topic |
single-channel recording calcium imaging TIRFM N-type Ca2+ channels |
spellingShingle |
single-channel recording calcium imaging TIRFM N-type Ca2+ channels DEMURO,ANGELO PARKER,IAN Imaging single-channel calcium microdomains by total internal reflection microscopy |
description |
The microdomains of Ca2+ in the cytosol around the mouth of open Ca2+ channels are the basic `building blocks' from which cellular Ca2+ signals are constructed. Moreover, the kinetics of local [Ca2+] closely reflect channel gating, so their measurement holds promise as an alternative to electrophysiological patch-clamp recording as a means to study single channel behavior. We have thus explored the development of optical techniques capable of imaging single-channel Ca2+ signals with good spatial and temporal resolution, and describe results obtained using total internal reflection fluorescence microscopy to monitor Ca2+ influx through single N-type channels expressed in Xenopus oocytes |
author |
DEMURO,ANGELO PARKER,IAN |
author_facet |
DEMURO,ANGELO PARKER,IAN |
author_sort |
DEMURO,ANGELO |
title |
Imaging single-channel calcium microdomains by total internal reflection microscopy |
title_short |
Imaging single-channel calcium microdomains by total internal reflection microscopy |
title_full |
Imaging single-channel calcium microdomains by total internal reflection microscopy |
title_fullStr |
Imaging single-channel calcium microdomains by total internal reflection microscopy |
title_full_unstemmed |
Imaging single-channel calcium microdomains by total internal reflection microscopy |
title_sort |
imaging single-channel calcium microdomains by total internal reflection microscopy |
publisher |
Sociedad de Biología de Chile |
publishDate |
2004 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000400025 |
work_keys_str_mv |
AT demuroangelo imagingsinglechannelcalciummicrodomainsbytotalinternalreflectionmicroscopy AT parkerian imagingsinglechannelcalciummicrodomainsbytotalinternalreflectionmicroscopy |
_version_ |
1718441378759835648 |