Site‐Selective Photo‐Crosslinking of Stilbene Pairs in a DNA Duplex Mediated by Ruthenium Photocatalyst

Author:

Kashida Hiromu1ORCID,Azuma Hidenori1,Sotome Hikaru2,Miyasaka Hiroshi2,Asanuma Hiroyuki1

Affiliation:

1. Department of Biomolecular Engineering Graduate School of Engineering Nagoya University Furo-cho, Chikusa-ku Nagoya 464-8603 Japan

2. Division of Frontier Materials Science and Center for Advanced Interdisciplinary Research Graduate School of Engineering Science Osaka University 1-3 Machikaneyama, Toyonaka Osaka 560-8531 Japan

Abstract

AbstractWe herein report a method for site‐selective photo‐crosslinking of a DNA duplex. A stilbene pair was introduced into a DNA duplex and a ruthenium complex was conjugated with a triplex‐forming oligonucleotide. We demonstrated that [2+2] photocycloaddition of the stilbene pair occurred upon irradiation with visible light when the ruthenium complex was in close proximity due to triplex formation. No reaction occurred when the ruthenium complex was not in proximity to the stilbene pair. The wavelength of visible light used was of lower energy than the wavelength of UV light necessary for direct excitation of stilbene. Quantum chemical calculation indicated that ruthenium complex catalyzed the photocycloaddition via triplet‐triplet energy transfer. Site selectivity of this photo‐crosslinking system was evaluated using a DNA duplex bearing two stilbene pairs as a substrate; we showed that the site of crosslinking was precisely regulated by the sequence of the oligonucleotide linked to the ruthenium complex. Since this method does not require orthogonal photoresponsive molecules, it will be useful in construction of complex photoresponsive DNA circuits, nanodevices and biological tools.

Funder

Japan Society for the Promotion of Science

Precursory Research for Embryonic Science and Technology

Japan Agency for Medical Research and Development

Publisher

Wiley

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