1 May 2008 Electron-multiplying charge-coupled detector-based bioluminescence recording of single-cell Ca2+
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The construction and application of genetically encoded intracellular calcium concentration ([Ca2+]i) indicators has a checkered history. Excitement raised over the creation of new probes is often followed by disappointment when it is found that the initial demonstrations of [Ca2+]i sensing capability cannot be leveraged into real scientific advances. Recombinant apo-aequorin cloned from Aequorea victoria was the first Ca2+ sensitive protein genetically targeted to subcellular compartments. In the jellyfish, bioluminescence resonance energy transfer (BRET) between Ca2+ bound aequorin and green fluorescent protein (GFP) emits green light. Similarly, Ca2+ sensitive bioluminescent reporters undergoing BRET have been constructed between aequorin and GFP, and more recently with other fluorescent protein variants. These hybrid proteins display red-shifted spectrums and have higher light intensities and stability compared to aequorin alone. We report BRET measurement of single-cell [Ca2+]i based on the use of electron-multiplying charge-coupled-detector (EMCCD) imaging camera technology, mounted on either a bioluminescence or conventional microscope. Our results show for the first time how these new technologies make facile long-term monitoring of [Ca2+]i at the single-cell level, obviating the need for expensive, fragile, and sophisticated equipment based on image-photon-detectors (IPD) that were until now the only technical recourse to dynamic BRET experiments of this type.
© (2008) Society of Photo-Optical Instrumentation Engineers (SPIE)
Kelly L. Rogers, Kelly L. Rogers, Jean-Rene Martin, Jean-Rene Martin, Olivier Renaud, Olivier Renaud, Eric Karplus, Eric Karplus, Marie-Anne Nicola, Marie-Anne Nicola, Marie Nguyen, Marie Nguyen, Sandrine Picaud, Sandrine Picaud, Spencer L. Shorte, Spencer L. Shorte, Philippe Brulet, Philippe Brulet, } "Electron-multiplying charge-coupled detector-based bioluminescence recording of single-cell Ca2+," Journal of Biomedical Optics 13(3), 031211 (1 May 2008). https://doi.org/10.1117/1.2937236 . Submission:


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