Controlling Pyrene Association in DNA Duplexes by B- to Z-DNA Transitions

被引:3
作者
Nakamura, Mitsunobu [1 ]
Takada, Tadao [1 ]
Yamana, Kazushige [1 ]
机构
[1] Univ Hyogo, Dept Appl Chem, 2167 Shosha, Himeji, Hyogo 6712280, Japan
基金
日本学术振兴会;
关键词
B-Z transitions; circular dichroism; DNA; fluorescence; pyrenes; EXCESS ELECTRON-TRANSFER; INTERSTRAND-STACKING; RNA DUPLEX; CRYSTAL-STRUCTURE; THIAZOLE ORANGE; BINDING; STABILIZATION; PORPHYRIN; HYBRIDIZATION; LUMINESCENCE;
D O I
10.1002/cbic.201900350
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
B- to Z-DNA transitions play a crucial role in biological systems and have attracted the interest of researchers for their applications in DNA nanotechnology. DNA and DNA analogues have also been used as templates to construct helical chromophore associations with pi interactions. In this work, the B- to Z-DNA transition-induced switching of pyrene in an association manner was evaluated using DNA duplexes with non-nucleosidic pyrene residues in the middle of d(CG) repeat sequences. One of the pyrene-labeled DNAs was shown to exhibit inverted exciton coupled circular dichroism signals upon pyrene association through a B- to Z-DNA transition. This observation indicates that pyrene association switches the DNA conformation from right- to left-handed. Interestingly, the fluorescence of the pyrene-labeled DNA duplex also dynamically changed upon switching of the pyrene in an association-based manner. Taken together, these studies demonstrate that pyrene-labeled DNA shows promise as a chiroptical molecular switch.
引用
收藏
页码:2949 / 2954
页数:6
相关论文
共 83 条
  • [1] [Anonymous], ANGEW CHEM
  • [2] Intrinsic Z-DNA Is Stabilized by the Conformational Selection Mechanism of Z-DNA-Binding Proteins
    Bae, Sangsu
    Kim, Doyoun
    Kim, Kyeong Kyu
    Kim, Yang-Gyun
    Hohng, Sungchul
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (04) : 668 - 671
  • [3] A cationic zinc porphyrin as a chiroptical probe for Z-DNA
    Balaz, M
    De Napoli, M
    Holmes, AE
    Mammana, A
    Nakanishi, K
    Berova, N
    Purrello, R
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (26) : 4006 - 4009
  • [4] Balaz M., 2005, ANGEW CHEM, V117, P4074
  • [5] Baumstark D., 2008, ANGEW CHEM, V120, P2652
  • [6] Fluorescent hydrophobic zippers inside duplex DNA:: Interstrand stacking of perylene-3,4:9,10-tetracarboxylic acid bisimides as artificial DNA base dyes
    Baumstark, Daniela
    Wagenknecht, Hans-Achim
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (22) : 6640 - 6645
  • [7] Perylene bisimide dimers as fluorescent "Glue" for DNA and for base-mismatch detection
    Baumstark, Daniela
    Wagenknecht, Hans-Achim
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (14) : 2612 - 2614
  • [8] CONFORMATION AND DYNAMICS OF A LEFT-HANDED Z-DNA HAIRPIN - STUDIES OF D(CGCGCGTTTTCGCGCG) IN SOLUTION
    BENIGHT, AS
    WANG, YS
    AMARATUNGA, M
    CHATTOPADHYAYA, R
    HENDERSON, J
    HANLON, S
    IKUTA, S
    [J]. BIOCHEMISTRY, 1989, 28 (08) : 3323 - 3332
  • [9] Berndl S., 2009, ANGEW CHEM, V121, P2454
  • [10] Thiazole Orange Dimers in DNA: Fluorescent Base Substitutions with Hybridization Readout
    Berndl, Sina
    Dimitrov, Stoichko D.
    Menacher, Florian
    Fiebig, Torsten
    Wagenknecht, Hans-Achim
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2016, 22 (07) : 2386 - 2395