Cross-talk and specificity in multi-color imaging experiments
Cross-talk between fluorescence channels is an important concern for multi-color imaging experiments. The detection of fluorescence from one dye in multiple detection channels can result in artifactual co-localization of signals. Cross-talk usually occurs because of the overlap of dye excitation and emission spectra, and can be managed by careful matching of dye selections to instrument filters, titration of probes to prevent overly bright signal, and imaging each channel individually to prevent cross-excitation by different laser lines. In any multi-color imaging experiment, single stain controls (separate samples stained with each probe by itself) are crucial for ensuring that cross-talk is minimized.
Photoconversion: an unexpected source of cross-talk from DAPI and Hoechst
Another source of cross-talk that researchers may be less familiar with is dye photoconversion. This is a change in the spectral properties of a fluorophore that results from its exposure to light. The commonly used blue fluorescent nuclear dyes DAPI and Hoechst undergo UV-induced photoconversion to form green-emitting fluorophores (Żurek-Biesiada et al. 2013). Many microscopists are accustomed to using epifluorescence with UV excitation to view and focus on Hoechst- or DAPI-stained nuclei before viewing fluorescence in other channels. This practice can cause DAPI and Hoechst to fluoresce in both the DAPI channel and the FITC channel. While it is much less bright than the original blue dye fluorescence, the green nuclear signal from the photoconversion product could interfere with imaging of green fluorescent probes like GFP or labeled antibodies, especially for low abundance targets, appearing as spurious nuclear localization.
Avoiding artifacts from DAPI and Hoechst
DAPI and Hoechst undergo photoconversion after exposure to UV wavelengths, but not longer excitation wavelengths such as FITC filter cubes or the 405 nm laser line. Once aware of the potential for photoconversion to green fluorescence, it is possible to avoid artifacts through careful imaging practices. One can image green fluorescence before switching to the DAPI channel, or move to an unexposed field of view before imaging the green channel after UV exposure of the sample. If confocal imaging using the 405 laser line is an option, it is possible to avoid the use of epifluorescence to detect DAPI or Hoechst altogether, which unfortunately sacrifices their utility as aids for finding and focusing on cells. Finally, it is important to include single stain controls for blue nuclear counterstains, especially when detecting low abundance or nuclear targets in the green channel.
RedDot™1 and RedDot™2 far-red nuclear counterstains
Alternative far-red nuclear counterstains, such as Biotium’s RedDot™1 and RedDot™2, avoid the problem of UV photoconversion of DAPI and Hoechst. RedDot™1 is cell-membrane permeable, and can be used a nuclear stain for live cells, while RedDot™2 is a counterstain for fixed and permeabilized cells. RedDot™2 is cell-membrane impermeable, and also can be used for selective staining of dead cells. One disadvantage of RedDot™1 is that it is more cytotoxic than the commonly used Hoechst 33342 (also available from Biotium), which remains the better choice for nuclear staining of cells that will be cultured for more than a few hours. Like all far-red dyes, RedDot™1 and RedDot™2 fluorescence is not visible to the human eye, and must be imaged using a CCD camera or confocal microscope in the Cy5 channel. On the plus side, RedDot™1 and RedDot™2 emission spectra are very well separated from green fluorescent dyes and probes, further reducing the potential for artifacts arising from fluorescence cross-talk. In addition, they leave the visible blue fluorescence channel free for detection of other targets.
Żurek-Biesiada, D., Kędracka-Krok, S. and Dobrucki, J. W. (2013), UV-activated conversion of Hoechst 33258, DAPI, and Vybrant DyeCycle fluorescent dyes into blue-excited, green-emitting protonated forms. Cytometry, 83A: 441–451. doi:10.1002/cyto.a.22260
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