Interaction between DNA and cationic metalloporphyrins in ionic liquid solutions

Author:

Nobuoka Kaoru1,Sumi Kensuke2,Kitagawa Eri2,Sato Kenta2,Nakamura Ayumi2,Kitaoka Satoshi3

Affiliation:

1. Division of Applied Chemistry, Department of Integrated Science and Technology, Faculty of Science and Technology, Oita University, 700 Dannoharu, Oita, 870-1192, Japan

2. Division of Applied Chemistry, Graduate School of Engineering, Oita University, 700 Dannoharu, Oita, 870-1192, Japan

3. Department of Biotechnology and Chemistry, Faculty of Engineering, Kindai University, 1 Takaya Umenobe, Higashi-Hiroshima City, Hiroshima 739-2116, Japan

Abstract

We studied the interaction of water-soluble cationic metalloporphyrins, [Formula: see text]Py and TMPyP, with the DNA double helix in ionic liquid solutions using CD and absorption spectra. The dispersibility of their porphyrin complexes was improved by electrostatic interactions of the anions of the ionic liquid. In the case of Cu(II) and Zn(II) complexes, the [Formula: see text]Py complexes with pyridinium cations attached to the meso-phenyl groups via methylene groups intercalated into the DNA double helix, while the compact TMPyP complexes with pyridinium cations at the meso-position could not interact with DNA. Thus, it was suggested that the solvation behavior by ionic liquids depends on the structure of the porphyrin and also affects its interaction with DNA. Neither Mn(III) complexes with axial ligands could interact with DNA, regardless of the presence of the ionic liquids, due to their steric hindrance.

Funder

JSPS KAKENHI

JST A-STEP

Publisher

World Scientific Pub Co Pte Ltd

Subject

General Chemistry

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