Curriculum Vitaes

Mitsunobu Nakamura

  (中村 光伸)

Profile Information

Affiliation
Associate Professor, Graduate School, of Engineering, University of Hyogo
Degree
(BLANK)

J-GLOBAL ID
200901063499685190
researchmap Member ID
1000214809

External link

Research Interests

 4

Papers

 92
  • Mitsunobu Nakamura, Hibiki Yoshioka, Tadao Takada
    ChemistrySelect, 7(29), Aug 5, 2022  Peer-reviewedCorresponding author
  • Tadao Takada, Nao Shimogaki, Moe Naruo, Mitsunobu Nakamura, Kazushige Yamana
    ChemPhotoChem, 6(8), Aug, 2022  
  • Tadao Takada, Koma Nishida, Yurika Honda, Aoi Nakano, Mitsunobu Nakamura, Shuya Fan, Kiyohiko Kawai, Mamoru Fujitsuka, Kazushige Yamana
    ChemBioChem, 22(17) 2729-2735, Sep 2, 2021  
  • M. Nakamura, T. Takada, K. Yamana
    ChemBioChem, 20(23) 2949-2954, 2019  Peer-reviewed
    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 π 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.
  • Mitsunobu Nakamura, Yuki Matsui, Tadao Takada, Kazushige Yamana
    ChemistrySelect, 4 1525-1529, 2019  Peer-reviewed
    The construction of zipper-like chromophore-arrays in the major groove of duplex DNA remains a challenge because only a few chromophores for this application have been discovered. To address the challenge, dual-chromophore labeled DNAs having a self-complementary sequence were prepared using a solid-phase, post-synthetic, copper-catalyzed, alkyne-azide cycloaddition. The resulting chromophore-arrays on the labeled DNA duplexes were characterized. The dual-tetraphenylethene (TPE) or dual-pyrene (Py) labeled DNA formed self-complementary B-form duplexes and resulted in the construction of chromophore-arrays in the major groove. The TPE-arrays, in which TPEs were arranged in a zipper-like fashion, slightly destabilized the duplex because of their bulkiness and exhibited aggregation-induced-emission. The Py-arrays, in which Pys were not arranged in a zipper-like fashion, had no effect on duplex stability and exhibited weak excimer emission because Py was sufficiently small for free rotation in the major groove.

Misc.

 10

Books and Other Publications

 6

Presentations

 6

Teaching Experience

 4

Research Projects

 13