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机构地区:[1]中国科学院生物物理研究所
出 处:《生物物理学报》1994年第2期317-322,共6页Acta Biophysica Sinica
基 金:国家自然科学基金
摘 要:研究了DNA与红细胞膜脂质过氧化产物的相互作用。与无DNA的反应体系相比,DNA的加入明显增加440nm处的荧光强度,这种效应是由于DNA与过氧红细胞膜生成了新的荧光物质,其激发波长315nm,发射波长410nm.维生素E强烈抑制荧光产物的形成。DNA经分离、纯化后用EB作荧光探针研究表明,DNA二级结构发生了改变,DNA—EB复合物荧光光谱,DNA—EB复合物之间的能量转移效率均有明显变化。同时证实DNA损伤具有碱基特异性,即主要是鸟嘌呤受到损伤。Interaction of DNA with peroxidizing erythrocyte membrane was studied. Compated with the system without DNA, the addition of DNA obviously enhance the fluorescence intensity at 440nm.It is due to the formation of new fluorescence product between DNA and peroxidizing erythrocyte membrane, with maximum excitation wavelength at 315um and maximum emission wavelength at 410nm. Vitamin E strongly inhibital the formation of fluorescence product. After DNA was separated and purified, and EB was used as fluoascent probe to detect the higher structure of DNA we found that fluorescent spectrum of DNA-EB changed obviously, and the energy transfer effichacy from DNA tO EB decreased , this showed that DNA was damaged. Among the four usual bases, guanine damage was much more serious than those of the other three.
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