DAPI

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DAPI
DAPI.svg
DAPI Space Fill.png
Names
IUPAC name
2-(4-Amidinophenyl)-1H-indole-6-carboxamidine
Other names
4',6-Diamidino-2-phenylindole
Identifiers
28718-90-3 YesY
ChEBI CHEBI:51231 YesY
ChEMBL ChEMBL48217 YesY
ChemSpider 2848 YesY
Jmol 3D model Interactive image
Interactive image
PubChem 2954
  • InChI=1S/C16H15N5/c17-15(18)10-3-1-9(2-4-10)13-7-11-5-6-12(16(19)20)8-14(11)21-13/h1-8,21H,(H3,17,18)(H3,19,20) YesY
    Key: FWBHETKCLVMNFS-UHFFFAOYSA-N YesY
  • InChI=1/C16H15N5/c17-15(18)10-3-1-9(2-4-10)13-7-11-5-6-12(16(19)20)8-14(11)21-13/h1-8,21H,(H3,17,18)(H3,19,20)
    Key: FWBHETKCLVMNFS-UHFFFAOYAH
  • [N@H]=C(N)c3ccc(c2cc1ccc(cc1n2)C(=[N@H])N)cc3
  • [H]/N=C(/c1ccc(cc1)c2cc3ccc(cc3[nH]2)/C(=N/[H])/N)\N
Properties
C16H15N5
Molar mass 277.33 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

DAPI (4',6-diamidino-2-phenylindole) is a fluorescent stain that binds strongly to A-T rich regions in DNA. It is used extensively in fluorescence microscopy. As DAPI can pass through an intact cell membrane, it can be used to stain both live and fixed cells, though it passes through the membrane less efficiently in live cells and therefore the effectiveness of the stain is lower.

History

DAPI was first synthesised in 1971 in the laboratory of Otto Dann as part of a search for drugs to treat trypanosomiasis. Although it was unsuccessful as a drug, further investigation indicated it bound strongly to DNA and became more fluorescent when bound. This led to its use in identifying mitochondrial DNA in ultracentrifugation in 1975, the first recorded use of DAPI as a fluorescent DNA stain.[1]

Strong fluorescence when bound to DNA led to the rapid adoption of DAPI for fluorescent staining of DNA for fluorescence microscopy. Its use for detecting DNA in plant, metazoa and bacteria cells and virus particles was demonstrated in the late 1970s, and quantitative staining of DNA inside cells was demonstrated in 1977. Use of DAPI as a DNA stain for flow cytometry was also demonstrated around this time.[1]

Fluorescence properties

When bound to double-stranded DNA DAPI has an absorption maximum at a wavelength of 358 nm (ultraviolet) and its emission maximum is at 461 nm (blue). Therefore for fluorescence microscopy DAPI is excited with ultraviolet light and is detected through a blue/cyan filter. The emission peak is fairly broad[2] DAPI will also bind to RNA, though it is not as strongly fluorescent. Its emission shifts to around 500 nm when bound to RNA.[3][4]

DAPI (magenta) bound to the minor groove of DNA (green and blue). From PDB: 1D30​.

DAPI's blue emission is convenient for microscopists who wish to use multiple fluorescent stains in a single sample. There is some fluorescence overlap between DAPI and green-fluorescent molecules like fluorescein and green fluorescent protein (GFP) but the effect of this is small. Use of spectral unmixing can account for this effect if extremely precise image analysis is required.

Outside of analytical fluorescence light microscopy DAPI is also popular for labeling of cell cultures to detect the DNA of contaminating mycoplasma or virus. The labelled mycoplasma or virus particles in the growth medium fluoresce once stained by DAPI making them easy to detect.[5]

Modelling of absorption and fluorescence properties

This DNA fluorescent probe has recently been effectively modeled [6] using the Time-dependent density functional theory, coupled with the IEF version of the Polarizable continuum model. This quantum-mechanical modeling has rationalized the absorption and fluorescence behavior given by minor groove binding and intercalation in the DNA pocket, in term of a reduced structural flexibility and polarization.

Live cells and toxicity

DAPI can be used for fixed cell staining. The concentration of DAPI needed for live cell staining is generally very high; it is rarely used for live cells.[7] It is labeled non-toxic in its MSDS[8] and though it was not shown to have mutagenicity to E. coli,[9] it is labelled as a known mutagen in manufacturer information.[2] As it is a DNA binding compound, it is likely to have some low level mutagenic properties and care should be taken in its handling and disposal.

Alternatives

Endothelial cells stained with DAPI (blue), phalloidin (red) and through immunofluorescence via an antibody bound to FITC (green).

The Hoechst stains are similar to DAPI in that they are also blue-fluorescent DNA stains which are compatible with both live- and fixed-cell applications, as well as visible using the same equipment filter settings as for DAPI.

Notes and references

  1. ↑ 1.0 1.1 Lua error in package.lua at line 80: module 'strict' not found.
  2. ↑ 2.0 2.1 Invitrogen, DAPI Nucleic Acid Stain. accessed 2009-12-08.
  3. ↑ Scott Prahl, DAPI. accessed 2009-12-08.
  4. ↑ Kapuscinski J., [1]. accessed 2013-02-25.
  5. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  6. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  7. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  8. ↑ http://www.kpl.com/docs/msds/710301.pdf
  9. ↑ Lua error in package.lua at line 80: module 'strict' not found.

See also

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