Calcein

Calcein
Identifiers
1461-15-0 Yes
ChEBI CHEBI:51903 Yes
ChEMBL ChEMBL1973733 
ChemSpider 58589 Yes
Jmol-3D images Image
Image
PubChem 65079
Properties
C30H26N2O13
Molar mass 622.55 g/mol
Melting point Decomposes
Boiling point N/A
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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Infobox references

Calcein, also known as fluorexon, fluorescein complex, is a fluorescent dye with excitation and emission wavelengths of 495/515 nm, respectively, and has the appearance of orange crystals. Calcein self-quenches at concentrations above 70mM and is commonly used as an indicator of lipid vesicle leakage.[1][2][3] It is also used traditionally as a complexometric indicator for titration of calcium ions with EDTA, and for fluorometric determination of calcium.

Applications

The acetomethoxy derivate of calcein (calcein AM) is used in biology as it can be transported through the cellular membrane into live cells, which makes it useful for testing of cell viability and for short-term labeling of cells. An acetomethoxy group obscures the part of the molecule that chelates Ca2+, Mg2+, Zn2+ and other ions. After transport into the cells, intracellular esterases remove the acetomethoxy group, the molecule gets trapped inside and gives out strong green fluorescence. As dead cells lack active esterases, only live cells are labeled[4] and counted by flow cytometry.

Calcein is now rarely used as a Ca2+ or Mg2+ indicator because its fluorescence is directly sensitive to these ions only at strongly alkaline pH, and thus it is not particularly useful for measuring Ca2+ or Mg2+ in cells. Fluorescence of calcein is quenched strongly by Co2+, Ni2+ and Cu2+ and appreciably by Fe3+ and Mn2+ at physiological pH. This fluorescence quenching response can be exploited for detecting the opening of the mitochondrial permeability transition pore and for measuring cell volume changes.[5] Calcein is commonly used for cell tracing and in studies of endocytosis and gap junctions.[6]

The acetoxymethyl ester of calcein is also used to detect drug interactions with multidrug resistance proteins (ABC transporters ATP-binding cassette transporter genes) in intact cells as it is an excellent substrate of the multidrug resistance transporter 1 (MDR1) P-glycoprotein and the Multidrug Resistance-Related Protein (MRP1).[7] The calcein AM assay can be used as a model for drug-drug interactions, for screening transporter substrates and/or inhibitors;[8] and also to determine in vitro drug resistance of cells, including samples from patients.[9][10]

Calcein is also used for marking freshly hatched fish[11] and for labeling of bones in live animals.

References

  1. Allen, T.M.; Cleland, L.G. "Serum-induced leakage of liposome contents". Biochimica et Biophysica Acta (BBA) - Biomembranes 597 (2): 418–426. doi:10.1016/0005-2736(80)90118-2.
  2. Sendai virus induced leakage of liposomes containing gangliosides Yung Shyeng Tsao and Leaf Huang Biochemistry 1985 24 (5), 1092-1098
  3. Patel, H.; Tscheka, C.; Heerklotz, H. (2009). "Characterizing vesicle leakage by fluorescence lifetime measurements". Soft Matter 5 (15): 2849–2851. doi:10.1039/B908524F.
  4. "How Light Microscopes Work". HowStuffWorks.
  5. Hamann, J.F.; Kiilgard; Litman, T.; Alvarez-Leefmans, J.; Zeuthen, T. (2002). "Measurement of cell volume changes by fluorescence self-quenching". J. Fluorescence 12 (2): 139–145. doi:10.1023/a:1016832027325.
  6. "Fluorescent Indicators for Zn2+ and Other Metal Ions—Section 19.7". Molecular Probes: The Handbook. invitrogen.
  7. Glavinas H, Krajcsi P, Cserepes J, Sarkadi B (January 2004). "The role of ABC transporters in drug resistance, metabolism and toxicity". Curr Drug Deliv 1 (1): 27–42. doi:10.2174/1567201043480036. PMID 16305368.
  8. more detailed description of the assay/ http://www.solvobiotech.com/technologies/dye-efflux
  9. a detailed description of the method http://www.solvobiotech.com/documents/MDQ_flyer.pdf
  10. Karászi E, Jakab K, Homolya L et al. (February 2001). "Calcein assay for multidrug resistance reliably predicts therapy response and survival rate in acute myeloid leukaemia". Br. J. Haematol. 112 (2): 308–14. doi:10.1046/j.1365-2141.2001.02554.x. PMID 11167823.
  11. "Marking fry using calcein". Game & Wildlife Conservation Trust.

Tomita et al. (2008) Loop-mediated isothermal amplification (LAMP) of gene sequences and simple visual detection of products, NATURE PROTOCOLS 3: 877-882.