Fluorescent complexes of DNA with DAPI 4',6-diamidine-2-phenyl indole.2HCl or DCI 4',6-dicarboxyamide-2-phenyl indole
- PMID: 31603
- PMCID: PMC342709
- DOI: 10.1093/nar/5.10.3775
Fluorescent complexes of DNA with DAPI 4',6-diamidine-2-phenyl indole.2HCl or DCI 4',6-dicarboxyamide-2-phenyl indole
Abstract
4',6-Dioarboxyamide-2-phenyl indole (DCI), a non-ionic structural analogue of 4',6-diamidine-2-phenyl indole.2HCl (DAPI), was synthesized in order to verify the hypothesis of intercalation of both dyes into the DNA double helix. The influence of pH, viscosity, and different concentrations of SDS (sodium dodecylsulphate) or NaCl on the optical and fluorescent properties and the changes in thermal transition of both dye complexes with DNA confirm the affinity of the dyes to the double helix as well as their stabilizing influence on the secondary DNA structure. The results of binding studies, carried out by fluorescent methods have shown that the dyes are strongly bound to DNA, though the number of binding sites is small. According to the experimental data, the fluorescent properties of DAPI and DCI complexes with DNA are connected with the intercalating binding mechanism of these dyes. On the other hand, the eventual ionic or hydrogen bonds of dyes outside the DNA helix do not change noticeably their fluorescent properties.
Similar articles
-
The fluorescence properties of a DNA probe. 4'-6-Diamidino-2-phenylindole (DAPI).Eur Biophys J. 1990;17(6):315-23. doi: 10.1007/BF00258380. Eur Biophys J. 1990. PMID: 2307139
-
DNA interaction with DAPI fluorescent dye: Force spectroscopy decouples two different binding modes.Biopolymers. 2017 May;107(5). doi: 10.1002/bip.23015. Biopolymers. 2017. PMID: 28124375
-
Selective staining by 4', 6-diamidine-2-phenylindole of nanogram quantities of DNA in the presence of RNA on gels.Nucleic Acids Res. 1979 Aug 10;6(11):3535-42. doi: 10.1093/nar/6.11.3535. Nucleic Acids Res. 1979. PMID: 493114 Free PMC article.
-
DAPI: a DNA-specific fluorescent probe.Biotech Histochem. 1995 Sep;70(5):220-33. doi: 10.3109/10520299509108199. Biotech Histochem. 1995. PMID: 8580206 Review.
-
Analysing DNA complexes by circular and linear dichroism.J Mol Recognit. 1994 Jun;7(2):141-55. doi: 10.1002/jmr.300070211. J Mol Recognit. 1994. PMID: 7826674 Review.
Cited by
-
Mode of treatment governs curcumin response on doxorubicin-induced toxicity in cardiomyoblasts.Mol Cell Biochem. 2018 May;442(1-2):81-96. doi: 10.1007/s11010-017-3195-6. Epub 2017 Sep 19. Mol Cell Biochem. 2018. PMID: 28929270
-
Dielectrophoresis based discrimination of human embryonic stem cells from differentiating derivatives.Biomicrofluidics. 2012 Dec 12;6(4):44113. doi: 10.1063/1.4771316. eCollection 2012. Biomicrofluidics. 2012. PMID: 24339846 Free PMC article.
-
Rapid determination of the active fraction of DNA repair glycosylases: a novel fluorescence assay for trapped intermediates.Nucleic Acids Res. 2007;35(5):1601-11. doi: 10.1093/nar/gkm021. Epub 2007 Feb 8. Nucleic Acids Res. 2007. PMID: 17289752 Free PMC article.
-
P2X(7) nucleotide receptors mediate caspase-8/9/3-dependent apoptosis in rat primary cortical neurons.Purinergic Signal. 2005 Dec;1(4):337-47. doi: 10.1007/s11302-005-7145-5. Epub 2005 Dec 3. Purinergic Signal. 2005. PMID: 18404518 Free PMC article.
-
Evaluation of Oxidative Stress in Mammalian Spermatozoa.Methods Mol Biol. 2025;2897:363-415. doi: 10.1007/978-1-0716-4406-5_26. Methods Mol Biol. 2025. PMID: 40202649
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources