Literature DB >> 23124113

Capturing single L-type Ca(2+) channel function with optics.

Matthew A Nystoriak1, Madeline Nieves-Cintrón, Manuel F Navedo.   

Abstract

Advances in imaging technology have allowed optical analysis of Ca(2+)-permeable ion channel activity. Here, we briefly review novel developments in optical recording of L-type voltage-dependent Ca(2+) channel (LTCC) function with high spatial and temporal resolution. Underlying principles supporting the use of total internal reflection fluorescence (TIRF) microscopy for optical measurement of channel activity and new functional characteristics of LTCCs revealed by application of this approach are discussed. Visualization of Ca(2+) influx through single LTCCs ("LTCC sparklets") has demonstrated that channel activity is regionally heterogeneous and that clustered channels are capable of operating in a cooperative, or "coupled" manner. In light of these findings, we describe a current molecular model for the local control of LTCC activity and coupled gating in physiological and pathological contexts. This article is part of a Special Issue entitled: 12th European Symposium on Calcium.
Copyright © 2012 Elsevier B.V. All rights reserved.

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Year:  2012        PMID: 23124113      PMCID: PMC3574202          DOI: 10.1016/j.bbamcr.2012.10.027

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  78 in total

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7.  Spinning-Spot Shadowless TIRF Microscopy.

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8.  Dynamic L-type CaV1.2 channel trafficking facilitates CaV1.2 clustering and cooperative gating.

Authors:  Debapriya Ghosh; Madeline Nieves-Cintrón; Sendoa Tajada; Ingrid Brust-Mascher; Mary C Horne; Johannes W Hell; Rose E Dixon; Luis F Santana; Manuel F Navedo
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  8 in total

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