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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Autores principales: DEMURO,ANGELO, PARKER,IAN
Lenguaje:English
Publicado: Sociedad de Biología de Chile 2004
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Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000400025
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spelling 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
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