Hirakawa Kazutaka, Hirano Toru
Department of Basic Engineering (Chemistry), Faculty of Engineering, Shizuoka University, Shizuoka, Japan.
Photochem Photobiol. 2008 Jan-Feb;84(1):202-8. doi: 10.1111/j.1751-1097.2007.00220.x.
The effect of the interaction between DNA and the photosensitizer on photosensitized singlet oxygen (1O2) generation was investigated using DNA-binding alkaloids, berberine and palmatine. These photosensitizers were bound to DNA by electrostatic force. Near-infrared luminescence measurement demonstrated that the photoexcited alkaloids can generate 1O2 only when the photosensitizers are bound to DNA. A fluorescence decay study showed significant enhancement of the lifetime of their photoexcited state with the DNA binding. A calculation study suggested that the electrostatic interaction with DNA inhibits the quenching of the photoexcited state of these alkaloids via intramolecular electron transfer, leading to the prolongation of the lifetime of their excited state. This effect should enhance their intersystem crossing and the yield of energy transfer to molecular oxygen. The results show that the electrostatic interaction with DNA significantly affects the 1O2 generation activity of a photosensitizer. In addition, this interaction may be applied to the control and the design of photosensitizers for medical applications such as photodynamic therapy.
使用与DNA结合的生物碱黄连素和巴马汀,研究了DNA与光敏剂之间的相互作用对光敏单线态氧(1O2)生成的影响。这些光敏剂通过静电力与DNA结合。近红外发光测量表明,只有当光敏剂与DNA结合时,光激发的生物碱才能产生1O2。荧光衰减研究表明,随着与DNA的结合,它们光激发态的寿命显著延长。一项计算研究表明,与DNA的静电相互作用通过分子内电子转移抑制了这些生物碱光激发态的猝灭,从而延长了它们激发态的寿命。这种效应应该会增强它们的系间窜越以及向分子氧的能量转移产率。结果表明,与DNA的静电相互作用显著影响光敏剂的1O2生成活性。此外,这种相互作用可应用于光动力疗法等医学应用中光敏剂的控制和设计。