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...

Full description

Bibliographic Details
Main Authors: ANGELO DEMURO, IAN PARKER
Format: Article
Language:English
Published: BMC 2004-01-01
Series:Biological Research
Subjects:
Online Access:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000400025
_version_ 1819261842455789568
author ANGELO DEMURO
IAN PARKER
author_facet ANGELO DEMURO
IAN PARKER
author_sort ANGELO DEMURO
collection DOAJ
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
first_indexed 2024-12-23T19:48:13Z
format Article
id doaj.art-60ce77ea5c22409caf5a6e45c35a94f8
institution Directory Open Access Journal
issn 0716-9760
0717-6287
language English
last_indexed 2024-12-23T19:48:13Z
publishDate 2004-01-01
publisher BMC
record_format Article
series Biological Research
spelling doaj.art-60ce77ea5c22409caf5a6e45c35a94f82022-12-21T17:33:27ZengBMCBiological Research0716-97600717-62872004-01-01374675679Imaging single-channel calcium microdomains by total internal reflection microscopyANGELO DEMUROIAN PARKERThe 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 oocyteshttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000400025single-channel recordingcalcium imagingTIRFMN-type Ca2+ channels
spellingShingle ANGELO DEMURO
IAN PARKER
Imaging single-channel calcium microdomains by total internal reflection microscopy
Biological Research
single-channel recording
calcium imaging
TIRFM
N-type Ca2+ channels
title 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_short Imaging single-channel calcium microdomains by total internal reflection microscopy
title_sort imaging single channel calcium microdomains by total internal reflection microscopy
topic single-channel recording
calcium imaging
TIRFM
N-type Ca2+ channels
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602004000400025
work_keys_str_mv AT angelodemuro imagingsinglechannelcalciummicrodomainsbytotalinternalreflectionmicroscopy
AT ianparker imagingsinglechannelcalciummicrodomainsbytotalinternalreflectionmicroscopy