Fluorescein isothiocyanate
5-FITC
6-FITC
Names
Other names
FITC
5-Isomer:
  • Fluorescein 5-isothiocyanate
  • Fluorescein isothiocyanate isomer I
  • 5-FITC
  • FITC-I

6-Isomer:
  • Fluorescein 6-isothiocyanate
  • Fluorescein isothiocyanate isomer II
  • 6-FITC
  • FITC-II
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.043.810
MeSH Fluorescein+isothiocyanate
UNII
  • InChI=1S/C21H11NO5S/c23-12-2-5-16-18(8-12)26-19-9-13(24)3-6-17(19)21(16)15-4-1-11(22-10-28)7-14(15)20(25)27-21/h1-9,23-24H
    Key: MHMNJMPURVTYEJ-UHFFFAOYSA-N checkY
  • InChI=1S/C21H11NO5S/c23-12-2-5-15-18(8-12)26-19-9-13(24)3-6-16(19)21(15)17-7-11(22-10-28)1-4-14(17)20(25)27-21/h1-9,23-24H checkY
    Key: GTQFZXYECNSNNC-UHFFFAOYSA-N checkY
  • c1cc2c(cc1N=C=S)C(=O)OC23c4ccc(cc4Oc5c3ccc(c5)O)O
  • c1cc2c(cc1N=C=S)C3(c4ccc(cc4Oc5c3ccc(c5)O)O)OC2=O
Properties
C21H11NO5S
Molar mass 389.38 g·mol−1
Density 1.542 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Fluorescein isothiocyanate (FITC) is a derivative of fluorescein used in wide-ranging applications[1][2] including flow cytometry. First described in 1942,[3] FITC is the original fluorescein molecule functionalized with an isothiocyanate reactive group (−N=C=S), replacing a hydrogen atom on the bottom ring of the structure. It is typically available as a mixture of isomers, fluorescein 5-isothiocyanate (5-FITC) and fluorescein 6-isothiocyanate (6-FITC). FITC is reactive towards nucleophiles including amine and sulfhydryl groups on proteins. It was synthesized by Robert Seiwald and Joseph Burckhalter in 1958. [4]

A succinimidyl-ester functional group attached to the fluorescein core, creating "NHS-fluorescein", forms another common amine reactive derivative that has much greater specificity toward primary amines in the presence of other nucleophiles.

FITC has excitation and emission spectrum peak wavelengths of approximately 495 nm and 519 nm,[5] giving it a green color. Like most fluorochromes, it is prone to photobleaching. Due to the problem of photobleaching, derivatives of fluorescein such as Alexa 488 and DyLight 488 have been tailored for various chemical and biological applications where greater photostability, higher fluorescence intensity, or different attachment groups are needed. In addition, some experiments make use of FITC's propensity for photobleaching in order to measure proteins' lateral mobility in membranes, through the technique of fluorescence recovery after photobleaching.[6]

References

  1. ↑ The TH; Feltkamp, T. E. (1970). "Conjugation of fluorescein isothiocyanate to antibodies: I. Experiments on the conditions of conjugation". Immunology. 18 (6): 865–873. PMC 1455721. PMID 5310665.
  2. ↑ The TH; Feltkamp, T. E. (1970). "Conjugation of fluorescein isothiocyanate to antibodies: II. A reproducible method". Immunology. 18 (6): 875–881. PMC 1455722. PMID 4913804.
  3. ↑ Coons AH, Creech HJ, Norman Jones R, Berliner E (1942). "The Demonstration of Pneumococcal Antigen in Tissues by the Use of Fluorescent Antibody". The Journal of Immunology. 45 (3): 159–170. doi:10.4049/jimmunol.45.3.159. S2CID 255685595.
  4. ↑ Riggs JL, Seiwald RJ, Burckhalter JH (1958). "Isothiocyanate Compounds as Fluorescent Labeling Agents for Immune Serum". The American Journal of Pathology. 34 (6): 1081–1097. PMC 1934794. PMID 13583098.
  5. ↑ "FITC".
  6. ↑ Tsuji, Akihiko; Ohnishi, Shunichi (1986-10-07). "Restriction of the lateral motion of band 3 in the erythrocyte membrane by the cytoskeletal network: dependence on spectrin association state". Biochemistry. 25 (20): 6133–6139. doi:10.1021/bi00368a045. ISSN 0006-2960. PMID 3790510.
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