School of Life Science and Technology, Tokyo Institute of Technology, J2-10 4259, Nagatsuta, Midoriku, Yokohama, 226-8501, Japan.
Sci Rep. 2023 Jan 23;13(1):288. doi: 10.1038/s41598-023-27526-2.
To realize nucleic acid-targeting photodynamic therapy, a photosensitizer should be attached at the optimal position on a complementary oligonucleotide, where a guanine photooxidation is maximized. Here we show the photooxidation of 22 DNA duplexes with varied lengths between a O-generating biphenyl photosensitizer attached at a midchain thymine in a strand and the single guanine reactant in the other strand. The best photooxidation efficiencies are achieved at 9, 10, and 21 base intervals, which coincides with the pitch of 10.5 base pairs per turn in a DNA duplex. The low efficiencies for near and far guanines are due to quenching of the biphenyl by guanine and dilution of O by diffusion, respectively. The O-diffusion mapping along DNA duplex provides clues to the development of efficient and selective photosensitizer agents for nucleic acid-targeting photodynamic therapy, as well as an experimental demonstration of diffusion of a particle along cylindrical surface in molecular level.
为了实现核酸靶向光动力疗法,应该将光敏剂附着在互补寡核苷酸的最佳位置上,在该位置上最大限度地进行鸟嘌呤光氧化。在这里,我们展示了连接在链中中链胸腺嘧啶上的生成 O 的联苯光敏剂与另一条链中单个鸟嘌呤反应物之间的 22 个 DNA 双链体的光氧化。在 9、10 和 21 个碱基间隔处获得最佳的光氧化效率,这与 DNA 双链体每转 10.5 个碱基对的螺距相吻合。近侧和远侧鸟嘌呤的低效率归因于鸟嘌呤对联苯的猝灭和 O 通过扩散的稀释。沿着 DNA 双链体的 O 扩散映射为开发用于核酸靶向光动力疗法的高效和选择性光敏剂提供了线索,同时也在分子水平上展示了粒子沿着圆柱表面的扩散的实验证明。