Literature DB >> 23681544

Imaging changes in cytoplasmic calcium using the Yellow Cameleon 3.6 biosensor and confocal microscopy.

Sarah J Swanson1, Simon Gilroy.   

Abstract

Changes in the concentration of cytoplasmic calcium, [Ca(2+)]cyt are central regulators in many cellular signal transduction pathways including many lipid-mediated regulatory networks. Given this central role that [Ca(2+)] has during plant growth, monitoring spatial and temporal [Ca(2+)] dynamics can reveal a critical component of cellular physiology. Here, we describe the measurement of [Ca(2+)]cyt in Arabidopsis root cells using plants expressing Yellow Cameleon 3.6 (YC 3.6). YC3.6 is a Ca(2+)-sensitive biosensor where the intensity of its fluorescence resonance energy transfer (FRET) signal changes as the Ca(2+) level within the cell rises and falls. The FRET from this calcium reporter can be visualized using confocal microscopy and the resultant images converted to a quantitative map of the levels of Ca(2+) using an approach called ratio analysis.

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Year:  2013        PMID: 23681544     DOI: 10.1007/978-1-62703-401-2_27

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Fluorescent Labeling and Confocal Microcopy of Plastids and Stromules.

Authors:  Maureen R Hanson; Patricia L Conklin; Amirali Sattarzadeh
Journal:  Methods Mol Biol       Date:  2021

Review 2.  Calcium imaging perspectives in plants.

Authors:  Chidananda Nagamangala Kanchiswamy; Mickael Malnoy; Andrea Occhipinti; Massimo E Maffei
Journal:  Int J Mol Sci       Date:  2014-03-04       Impact factor: 5.923

  2 in total

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