Changes in the concentration of cytoplasmic calcium, [Ca2+] cyt are central regulators in many cellular signal transduction pathways including many lipid-mediated regulatory networks. Given this central role that [Ca2+] has during plant growth, monitoring spatial and temporal [Ca2+] dynamics can reveal a critical component of cellular physiology. Here, we describe the measurement of [Ca2+]cyt in Arabidopsis root cells using plants expressing Yellow Cameleon 3.6 (YC 3.6). YC3.6 is a Ca2+-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 Ca2+ using an approach called ratio analysis. © 2013 Springer Science+Business Media, LLC.
CITATION STYLE
Swanson, S. J., & Gilroy, S. (2013). Imaging changes in cytoplasmic calcium using the yellow cameleon 3.6 biosensor and confocal microscopy. Methods in Molecular Biology, 1009, 291–302. https://doi.org/10.1007/978-1-62703-401-2_27
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