Literature DB >> 23064788

The hazards of DAPI photoconversion: effects of dye, mounting media and fixative, and how to minimize the problem.

Mojca Jež1, Tuba Bas, Matija Veber, Andrej Košir, Tanja Dominko, Raymond Page, Primož Rožman.   

Abstract

Immunocytochemistry is a powerful tool for detection and visualization of specific molecules in living or fixed cells, their localization and their relative abundance. One of the most commonly used fluorescent DNA dyes in immunocytochemistry applications is 4',6-diamidino-2-phenylindole dihydrochloride, known as DAPI. DAPI binds strongly to DNA and is used extensively for visualizing cell nuclei. It is excited by UV light and emits characteristic blue fluorescence. Here, we report a phenomenon based on an apparent photoconversion of DAPI that results in detection of a DAPI signal using a standard filter set for detection of green emission due to blue excitation. When a sample stained with DAPI only was first imaged with the green filter set (FITC/GFP), only a weak cytoplasmic autofluorescence was observed. Next, we imaged the sample with a DAPI filter set, obtaining a strong nuclear DAPI signal as expected. Upon reimaging the same samples with a FITC/GFP filter set, robust nuclear fluorescence was observed. We conclude that excitation with UV results in a photoconversion of DAPI that leads to detection of DAPI due to excitation and emission in the FITC/GFP channel. This phenomenon can affect data interpretation and lead to false-positive results when used together with fluorochrome-labeled nuclear proteins detected with blue excitation and green emission. In order to avoid misinterpretations, extra precaution should be taken to prepare staining solutions with low DAPI concentration and DAPI (UV excitation) images should be acquired after all other higher wavelength images. Of various DNA dyes tested, Hoechst 33342 exhibited the lowest photoconversion while that for DAPI and Hoechst 33258 was much stronger. Different fixation methods did not substantially affect the strength of photoconversion. We also suggest avoiding the use of mounting medium with high glycerol concentrations since glycerol showed the strongest impact on photoconversion. This photoconversion effect cannot be avoided even when using narrow bandpass filter sets.

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Year:  2012        PMID: 23064788     DOI: 10.1007/s00418-012-1039-8

Source DB:  PubMed          Journal:  Histochem Cell Biol        ISSN: 0948-6143            Impact factor:   4.304


  40 in total

Review 1.  Overview of cell fixatives and cell membrane permeants.

Authors:  M A Melan
Journal:  Methods Mol Biol       Date:  1999

2.  DAPI (4',6-diamidino-2-phenylindole) binds differently to DNA and RNA: minor-groove binding at AT sites and intercalation at AU sites.

Authors:  F A Tanious; J M Veal; H Buczak; L S Ratmeyer; W D Wilson
Journal:  Biochemistry       Date:  1992-03-31       Impact factor: 3.162

3.  Photoconversion of DAPI following UV or violet excitation can cause DAPI to fluoresce with blue or cyan excitation.

Authors:  M Piterburg; H Panet; A Weiss
Journal:  J Microsc       Date:  2012-01-31       Impact factor: 1.758

Review 4.  A guide to the perplexed on the specificity of antibodies.

Authors:  Clifford B Saper
Journal:  J Histochem Cytochem       Date:  2008-10-14       Impact factor: 2.479

5.  Multiple binding modes for Hoechst 33258 to DNA.

Authors:  T Stokke; H B Steen
Journal:  J Histochem Cytochem       Date:  1985-04       Impact factor: 2.479

6.  Nuclear position in the cells of the mouse early embryo.

Authors:  W J Reeve; F P Kelly
Journal:  J Embryol Exp Morphol       Date:  1983-06

7.  Analysis and sorting of living cells according to deoxyribonucleic acid content.

Authors:  D J Arndt-Jovin; T M Jovin
Journal:  J Histochem Cytochem       Date:  1977-07       Impact factor: 2.479

8.  Characterization of interaction between DNA and 4',6-diamidino-2-phenylindole by optical spectroscopy.

Authors:  M Kubista; B Akerman; B Nordén
Journal:  Biochemistry       Date:  1987-07-14       Impact factor: 3.162

9.  Analysis of apoptosis by cytometry using TUNEL assay.

Authors:  Zbigniew Darzynkiewicz; Dariusz Galkowski; Hong Zhao
Journal:  Methods       Date:  2008-03       Impact factor: 3.608

10.  Rapid, one step staining procedures for analysis of cellular DNA and protein by single and dual laser flow cytometry.

Authors:  H A Crissman; J A Steinkamp
Journal:  Cytometry       Date:  1982-09
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  8 in total

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2.  Photoconversion of DAPI and Hoechst dyes to green and red-emitting forms after exposure to UV excitation.

Authors:  Travis J Karg; Kent G Golic
Journal:  Chromosoma       Date:  2017-12-12       Impact factor: 4.316

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5.  Penetration of Carbon Nanotubes into the Retinoblastoma Tumor after Intravitreal Injection in LH BETA T AG Transgenic Mice Reti-noblastoma Model.

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6.  The study of protein recruitment to laser-induced DNA lesions can be distorted by photoconversion of the DNA binding dye Hoechst.

Authors:  Verena Hurst; Susan M Gasser
Journal:  F1000Res       Date:  2019-01-25

7.  Novel Synthesized N-Ethyl-Piperazinyl-Amides of C2-Substituted Oleanonic and Ursonic Acids Exhibit Cytotoxic Effects through Apoptotic Cell Death Regulation.

Authors:  Oxana Kazakova; Alexandra Mioc; Irina Smirnova; Irina Baikova; Adrian Voicu; Lavinia Vlaia; Ioana Macașoi; Marius Mioc; George Drăghici; Ştefana Avram; Cristina Dehelean; Codruța Şoica
Journal:  Int J Mol Sci       Date:  2021-10-11       Impact factor: 5.923

8.  DNA damage causes rapid accumulation of phosphoinositides for ATR signaling.

Authors:  Yu-Hsiu Wang; Anushya Hariharan; Giulia Bastianello; Yusuke Toyama; G V Shivashankar; Marco Foiani; Michael P Sheetz
Journal:  Nat Commun       Date:  2017-12-14       Impact factor: 14.919

  8 in total

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