Temporally and spatially defined changes in cellular calcium (Ca2+) concentration represent stimulusspecific signals and regulate a myriad of biological processes. The development of ratiometric Ca2+reporter proteins like Yellow Cameleons (YCs) has greatly advanced our ability to analyze Ca2+dynamics in vivo with unprecedented spatial and temporal resolution. In plants, the application of these Ca2+reporter proteins has been pioneered for the investigation of Ca2+dynamics in guard cells, and recently their use has been extended to other single-cell models like growing pollen tubes and root hairs. However, in plants, the use of YC reporter proteins has largely remained restricted to the investigation of cytoplasmic alterations of Ca2+concentrations. Here, we provide an introduction to current methods for imaging Ca2+dynamics with increasing sophistication. © 2013 Cold Spring Harbor Laboratory Press.
CITATION STYLE
Behera, S., Krebs, M., Loro, G., Schumacher, K., Costa, A., & Kudla, J. (2013, August). Ca2+ imaging in plants using genetically encoded yellow Cameleon Ca2+ indicators. Cold Spring Harbor Protocols. https://doi.org/10.1101/pdb.top066183
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