Biopolym. Cell. 2000; 16(5):345-355.
Structure and Function of Biopolymers
Interaction of cyanine dyes with nucleic acids. 14. Spectral peculiarities of several monomethyne benzothiazole cyanine dyes and their interaction with DNA
1Ogul'chansky T. Yu., 1Yashchuk V. M., 2Yarmoluk S. M., 1Losytskyy M. Yu.
  1. Institute of Molecular Biology and Genetics, NAS of Ukraine
    150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03680
  2. Taras Shevchenko National University of Kyiv
    64, Volodymyrska Str., Kyiv, Ukraine, 01033

Abstract

Absorption, fluorescence emission and excitation spectra of solutions of monomethyne benzothiazole cyanine dyes – thiazole orange (TO), Cyan 40 and Cyan 13 – have been studied in a wide concentration range in the presence and without DNA. It has been established that both molecular and aggregate absorption as well as both molecular and aggregate fluorescence are observed for the solutions of the dyes investigated, the aggregates electron system being essentially transformed after photon absorption. It has been shown that the own fluorescence of dye molecules dominates in emission of the investigated dye solutions with DNA. Its considerable quantum yield can be explained by the dye molecule fixation on the DNA molecule. The concentration auenching of this fluorescence has been found and it is accompanied with the appearance of a new absorption band. It has been supposed that the aggregates consisting of dye molecules fixed on DNA and free dye molecules are formed. On the ground of the data obtained we have concluded that the dye molecules interact through half-intercalation mode with DNA molecules and that the model of full intercalation is inapplicable to the interaction of the dyes investigated with DNA molecules.

References

[1] Dobretsov GE. Fluorescent probes in the study of cell membranes and lipoproteins. Moscow: Nauka, 1989. 277 p.
[2] Demchenko AP. Luminescence and dynamics of proteins structure. Kyiv, Naukova Dumka, 1988; 280 p
[3] Rye HS, Yue S, Wemmer DE, Quesada MA, Haugland RP, Mathies RA, Glazer AN. Stable fluorescent complexes of double-stranded DNA with bis-intercalating asymmetric cyanine dyes: properties and applications. Nucleic Acids Res. 1992;20(11):2803-12.
[4] Skeidsvoll J, Ueland PM. Analysis of double-stranded DNA by capillary electrophoresis with laser-induced fluorescence detection using the monomeric dye SYBR green I. Anal Biochem. 1995;231(2):359-65.
[5] Suzuki T, Fujikura K, Higashiyama T, Takata K. DNA staining for fluorescence and laser confocal microscopy. J Histochem Cytochem. 1997;45(1):49-53.
[6] Lerman LS. The structure of the DNA-acridine complex. Proc Natl Acad Sci U S A. 1963;49:94-102.
[7] Long EC, Barton JK. On demonstrating DNA intercalation. Acc Chem Res. 1990;23(9):271–3.
[8] Lee LG, Chen CH, Chiu LA. Thiazole orange: a new dye for reticulocyte analysis. Cytometry. 1986;7(6):508-17.
[9] Rye HS, Glazer AN. Interaction of dimeric intercalating dyes with single-stranded DNA. Nucleic Acids Res. 1995;23(7):1215-22.
[10] Yarmoluk SM, Kovalska VB, Smirnova TV, Shandura MP, Kovtun YP, Matsuka GKh. Interaction of cyanine dyes with nucleic acids. 2. Spectroscopic properties of methyleneoxy analogues of Thiazole Orange. Biopolym Cell. 1996; 12(6):74-81.
[11] Yarmoluk SM, Kovalska VB, Kovtun YuP. Interaction of cyanine dyes with nucleic acids. 5. Towards model of «half intercalation of monomethyne cyanine dyes into double-stranded nucleic acids. Biopolym Cell. 1999; 15(1):75-82.
[12] Kumar CV, Turner RS, Asuncion EH. Groove binding of a styrylcyanine dye to the DNA double helix: the salt effect. J Photochem Photobiol A Chem. 1993;74(2-3):231–8.
[13] Emerson ES, Conlin MA, Rosenoff AE, Norland KS, Rodriguez H, Chin D, et al. The geometrical structure and absorption spectrum of a cyanine dye aggregate. J Phys Chem. 1967;71(8):2396–403.