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蛋白质是羟基自由基主要的初始细胞靶点。

Proteins are major initial cell targets of hydroxyl free radicals.

作者信息

Du Juan, Gebicki Janusz M

机构信息

Department of Biological Sciences, Macquarie University, Sydney, NSW 2109, Australia.

出版信息

Int J Biochem Cell Biol. 2004 Nov;36(11):2334-43. doi: 10.1016/j.biocel.2004.05.012.

Abstract

The principal aim of the current study was to identify the initial cell targets of hydroxyl free radicals. Our recent report showed that proteins were oxidized before lipids in U937 cells exposed to peroxyl radicals. Extending this finding, we investigated whether a similar oxidation sequence occurs in other lines of cells, whether hydroxyl radicals can also initiate cell protein oxidation, and whether DNA fragmentation is an early event in radical-induced cell damage. Mouse myeloma Sp2/0-Ag14 and U937 cells were exposed to hydroxyl radicals generated in solution by gamma irradiation and the formation of protein peroxides measured by a ferric-xylenol orange assay. No lipid peroxidation or DNA damage was evident by the time of significant formation of protein peroxides. DNA fragmentation was detectable after prolonged incubation at 37 degrees C and was characteristic of enzymatic action rather than of random scission by the radicals. Yields of protein hydroperoxides in the irradiated cells were independent of composition of the medium, suggesting that only the radicals produced within the cells or immediately near the cell surface were effective in oxidizing the cell proteins. The results are consistent with the hypothesis that proteins are major initial targets of free radicals in cells and suggest that treatments leading to the prevention of protein oxidation or to harmless reduction of protein peroxides is likely to result in alleviation of radical-induced biological damage.

摘要

本研究的主要目的是确定羟基自由基的初始细胞靶点。我们最近的报告显示,在暴露于过氧自由基的U937细胞中,蛋白质比脂质先被氧化。基于这一发现,我们研究了在其他细胞系中是否也会出现类似的氧化顺序,羟基自由基是否也能引发细胞蛋白质氧化,以及DNA片段化是否是自由基诱导细胞损伤的早期事件。将小鼠骨髓瘤Sp2/0-Ag14细胞和U937细胞暴露于由γ射线照射在溶液中产生的羟基自由基,并通过铁-二甲苯酚橙测定法测量蛋白质过氧化物的形成。在蛋白质过氧化物大量形成时,未观察到脂质过氧化或DNA损伤。在37℃长时间孵育后可检测到DNA片段化,其具有酶促作用的特征,而非自由基随机断裂的特征。照射后细胞中蛋白质氢过氧化物的产量与培养基成分无关,这表明只有细胞内或细胞表面附近产生的自由基才能有效地氧化细胞蛋白质。这些结果与蛋白质是细胞内自由基主要初始靶点的假设一致,并表明导致预防蛋白质氧化或无害地还原蛋白质过氧化物的处理可能会减轻自由基诱导的生物损伤。

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