Analysis of Coherent Heteroclustering of Different Dyes by Use of Threoninol Nucleotides for Comparison with the Molecular Exciton Theory

被引:68
作者
Fujii, Taiga [1 ]
Kashida, Hiromu [1 ]
Asanuma, Hiroyuki [1 ,2 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Dept Mol Design & Engn, Chikusa Ku, Nagoya, Aichi 46, Japan
[2] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
DNA; exciton theory; heteroclusters; NMR spectroscopy; UV/Vis spectroscopy; SPECTROSCOPIC PROPERTIES; INTERSTRAND-STACKING; ENERGY-TRANSFER; SENSITIVE DNA; AGGREGATION; FLUORESCENT; DUPLEXES; BEACONS; PROBES; ACID;
D O I
10.1002/chem.200900962
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To test the molecular exciton theory for heterodimeric chromophores, various heterodimers and clusters, ill which two different dyes were stacked alternately, were prepared by hybridizing two oligodeoxyribonucleotides (ODNs). each of which tethered a different dye on D-threoninol at the center of the strand. NMR analyses revealed that two different dyes Irons each strand were stacked antiparallel to each other in the duplex, and were located adjacent to the 5'-side of a natural nucleobase. The spectroscopic behavior of these heterodimers wits systematically examined as it function of the difference in the wavelength of the dye absorption maxima (Delta lambda(max)). WC found that the absorption spectrum of the heterodimer was significantly different from that of the simple sum of each monomeric dye in the single strand When azobenzene and Methyl Red, which have at 335 and 490 nm, respectively, in the single strand (Delta lambda(max) = 144 nm), were assembled on ODNs, the bared derived from azobenzene exhibited a small hyperchromism. whereas the baled front,Methyl Red showed hypochromism and both bands shifted to a longer wavelength (bathochromism). These hyper- and hypochromisms were further enhanced ire a heterodimer derived from 4'-methylthioazobenzene: and Methyl Red, which had a much smaller Delta lambda(max) (82 nm: lambda(max) = 398 and 40 nm in the single-strand, respectively). With a combination of 4'-dimethyl-amino-2-nitroazobenzene and Methyl Red, which had an even smaller Delta lambda(max) (33 nm). a single sharp absorption baled that was apparently different from the SLIM of the. single-stranded spectra was observed. These changes ill the intensity of the absorption hand could he explained by the molecular exciton theory, which has been mainly applied to the spectral behavior of H- and/or J-aggregates composed of homo dyes. However, the bathochromic band shifts observed at shorter wavelegths did clot agree with the hypsochromisms predicted by the theory. Thus. these data experimentally verify the molecular exciton theory of heterodimerization This Coherent coupling anion, the heterodimers could also partly explain the bathochromicity and hypochromicity that were observed when the dyes were intercalated into the duplex.
引用
收藏
页码:10092 / 10102
页数:11
相关论文
共 51 条
[1]   DNA-Naphthyl Red conjugate as a visualizing probe of DNA hybridization [J].
Asanuma, H ;
Kashida, H ;
Liang, XG ;
Komiyama, M .
CHEMICAL COMMUNICATIONS, 2003, (13) :1536-1537
[2]   DNA-dye conjugates for controllable H* aggregation [J].
Asanuma, H ;
Shirasuka, K ;
Takarada, T ;
Kashida, H ;
Komiyama, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (08) :2217-2223
[3]   Highly Fluorescent Conjugated Pyrenes in Nucleic Acid Probes: (Phenylethynyl)pyrenecarbonyl-Functionalized Locked Nucleic Acids [J].
Astakhova, Irina V. ;
Korshun, Vladimir A. ;
Wengel, Jesper .
CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (35) :11010-11026
[4]   The native architecture of a photosynthetic membrane [J].
Bahatyrova, S ;
Frese, RN ;
Siebert, CA ;
Olsen, JD ;
van der Werf, KO ;
van Grondelle, R ;
Niederman, RA ;
Bullough, PA ;
Otto, C ;
Hunter, CN .
NATURE, 2004, 430 (7003) :1058-1062
[5]   Syntheses and energy transfer in multiporphyrinic arrays self-assembled with hydrogen-bonding recognition groups and comparison with covalent steroidal models [J].
Balaban, Teodor Silviu ;
Berova, Nina ;
Drain, Charles Michael ;
Hauschild, Robert ;
Huang, Xuefei ;
Kalt, Heinz ;
Lebedkin, Serri ;
Lehn, Jean-Marie ;
Nifaitis, Fotis ;
Pescitelli, Gennaro ;
Prokhorenko, Valentyn I. ;
Riedel, Gernot ;
Smeureanu, Gabriela ;
Zeller, Joachim .
CHEMISTRY-A EUROPEAN JOURNAL, 2007, 13 (30) :8411-8427
[6]  
BEINACCHI S, 2003, BIOPHYS J, V84, P643
[7]   VIOLET TO CYAN AZO DYES DERIVED FROM 4-AMINO-3-NITROBENZALDEHYDE AS DIAZO COMPONENT [J].
BELLO, KA ;
GRIFFITHS, J .
DYES AND PIGMENTS, 1989, 11 (01) :65-76
[8]  
Bernacchi S, 2001, Nucleic Acids Res, V29, pE62, DOI 10.1093/nar/29.13.e62
[9]  
BEROVA K, 2000, CIRCULAR DICHROISM P, P340
[10]   Dialkynylpyrenes: Strongly Fluorescent, Environment-Sensitive DNA Building Blocks [J].
Bittermann, Holger ;
Siegemund, Doreen ;
Malinovskii, Vladimir L. ;
Haener, Robert .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (46) :15285-+