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Interaction of cyanine dyes with nucleic acids. XXI. Arguments for half‐intercalation model of interaction
Author(s) -
Yarmoluk S. M.,
Lukashov S. S.,
Ogul'Chansky T. Yu.,
Losytskyy M. Yu.,
Kornyushyna O. S.
Publication year - 2001
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.1016
Subject(s) - chemistry , cyanine , benzothiazole , intercalation (chemistry) , steric effects , methylenedioxy , pyridine , fluorescence , dna , stereochemistry , photochemistry , molecule , benzimidazole , crystallography , medicinal chemistry , organic chemistry , alkoxy group , alkyl , biochemistry , physics , quantum mechanics
Abstract The spectral luminescent properties of two groups of monomethine cyanine dyes were studied in the presence of DNA. The first group included five dyes with 5,6‐methylenedioxy‐[ d ]‐benzo‐1,3‐thiazole heterocycle and their unsubstituted analogs. Five monomethine pyrylium cyanines and their N ‐methyl‐pyridine analogs were included in the second group. In each pair the pyrylium and pyridine dyes had similar geometry but differed in charge density distribution. The results presented some evidence in favor of the half‐intercalation interaction mode between the studied dyes and DNA. When the benzothiazole residue had the lowest electron donor ability between the two heterocycles in the dye molecule, its substitution with the bulky methylenedioxy group led to a significant decrease in fluorescence enhancement of the dye–DNA complex. On the contrary, when the substituents that create steric hindrance (e.g., methylenedioxy and methyl groups) were introduced into the heterocycle with the higher electron donor ability, the fluorescence enhancement value of the dye–DNA complex was virtually unchanged. The changes in the Stock's shift values upon the formation of the dye–DNA complexes were in agreement with the proposed half‐intercalation model. Interestingly, in the dye–DNA complexes the pyrylium dyes probably resided in a place similar to the pyridine ones. It is possible that the benzothiazole (or benzooxazole) ring intercalated between the DNA bases and the pyrylium (or pyridine) residue was located in the DNA groove closer to the phosphate backbone. © 2001 John Wiley & Sons, Inc. Biopolymers (Biospectroscopy) 62: 219–227, 2001

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