The microenvironment of DNA switches the activity of singelt oxygen generation photosensitized by berberine and palmatine

被引:57
作者
Hirakawa, Kazutaka [1 ]
Hirano, Toru [2 ]
机构
[1] Shizuoka Univ, Fac Engn, Dept Basic Engn Chem, Shizuoka, Japan
[2] Univ Hamamatsu Sch Med, Photon Med Res Ctr, Shizuoka, Japan
关键词
D O I
10.1111/j.1751-1097.2007.00220.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effect of the interaction between DNA and the photosensitizer on photosensitized singlet Oxygen (102) 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 102 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 102 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.
引用
收藏
页码:202 / 208
页数:7
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