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A new generation of Ca2+ indicators with greatly improved fluorescence properties.
Open accessAbstract
A new family of highly fluorescent indicators has been synthesized for biochemical studies of the physiological role of cytosolic free Ca2+. The compounds combine an 8-coordinate tetracarboxylate chelating site with stilbene chromophores. Incorporation of the ethylenic linkage of the stilbene into a heterocyclic ring enhances the quantum efficiency and photochemical stability of the fluorophore. Compared to their widely used predecessor, "quin2", the new dyes offer up to 30-fold brighter fluorescence, major changes in wavelength not just intensity upon Ca2+ binding, slightly lower affinities for Ca2+, slightly longer wavelengths of excitation, and considerably improved selectivity for Ca2+ over other divalent cations. These properties, particularly the wavelength sensitivity to Ca2+, should make these dyes the preferred fluorescent indicators for many intracellular applications, especially in single cells, adherent cell layers, or bulk tissues.
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Metadata
- Authors
- Grynkiewicz, G., Poenie, M., & Tsien, R. Y.
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1985-03
- Volume
- 260
- Issue
- 6
- Pages
- 3440-3450
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W2141260882
- Cited by
- 21,607
- References
- 0
- FWCI
- 228.30
- Type
- journal article
- Language
- en
- Open access
- hybrid
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