• Media type: E-Article
  • Title: Generation of Red-Shifted Cameleons for Imaging Ca2+ Dynamics of the Endoplasmic Reticulum
  • Contributor: Waldeck-Weiermair, Markus; Bischof, Helmut; Blass, Sandra; Deak, Andras; Klec, Christiane; Graier, Thomas; Roller, Clara; Rost, Rene; Eroglu, Emrah; Gottschalk, Benjamin; Hofmann, Nicole; Graier, Wolfgang; Malli, Roland
  • Published: MDPI AG, 2015
  • Published in: Sensors, 15 (2015) 6, Seite 13052-13068
  • Language: English
  • DOI: 10.3390/s150613052
  • ISSN: 1424-8220
  • Origination:
  • Footnote:
  • Description: Cameleons are sophisticated genetically encoded fluorescent probes that allow quantifying cellular Ca2+ signals. The probes are based on Förster resonance energy transfer (FRET) between terminally located fluorescent proteins (FPs), which move together upon binding of Ca2+ to the central calmodulin myosin light chain kinase M13 domain. Most of the available cameleons consist of cyan and yellow FPs (CFP and YFP) as the FRET pair. However, red-shifted versions with green and orange or red FPs (GFP, OFP, RFP) have some advantages such as less phototoxicity and minimal spectral overlay with autofluorescence of cells and fura-2, a prominent chemical Ca2+ indicator. While GFP/OFP- or GFP/RFP-based cameleons have been successfully used to study cytosolic and mitochondrial Ca2+ signals, red-shifted cameleons to visualize Ca2+ dynamics of the endoplasmic reticulum (ER) have not been developed so far. In this study, we generated and tested several ER targeted red-shifted cameleons. Our results show that GFP/OFP-based cameleons due to miss-targeting and their high Ca2+ binding affinity are inappropriate to record ER Ca2+ signals. However, ER targeted GFP/RFP-based probes were suitable to sense ER Ca2+ in a reliable manner. With this study we increased the palette of cameleons for visualizing Ca2+ dynamics within the main intracellular Ca2+ store.
  • Access State: Open Access