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125I诱导的DNA双链断裂:用于中性滤膜洗脱技术的校准及与X射线诱导断裂的比较。

125I-induced DNA double strand breaks: use in calibration of the neutral filter elution technique and comparison with X-ray induced breaks.

作者信息

Radford I R, Hodgson G S

出版信息

Int J Radiat Biol Relat Stud Phys Chem Med. 1985 Oct;48(4):555-66. doi: 10.1080/09553008514551611.

Abstract

The neutral filter elution assay, for measurement of DNA double strand breakage, has been calibrated using mouse L cells and Chinese hamster V79 cells labelled with [125I]dUrd and then held at liquid nitrogen temperature to accumulate decays. The basis of the calibration is the observation that each 125I decay, occurring in DNA, produces a DNA double strand break. Linear relationships between 125I decays per cell and lethal lesions per cell (minus natural logarithm survival) and the level of elution, were found. Using the calibration data, it was calculated that the yield of DNA double strand breaks after X-irradiation of both cell types was from 6 to 9 X 10(-12) DNA double strand breaks per Gy per dalton of DNA, for doses greater than 6 Gy. Neutral filter elution and survival data for X-irradiated and 125I-labelled cells suggested that the relationships between lethal lesions and DNA double strand breakage were significantly different for both cell types. An attempt was made to study the repair kinetics for 125I-induced DNA double strand breaks, but was frustrated by the rapid DNA degradation which occurs in cells that have been killed by the freezing-thawing process.

摘要

用于测量DNA双链断裂的中性滤膜洗脱试验,已使用用[125I]脱氧尿苷标记、然后保存在液氮温度下以累积衰变的小鼠L细胞和中国仓鼠V79细胞进行了校准。校准的基础是观察到发生在DNA中的每一次125I衰变都会产生一个DNA双链断裂。发现了每个细胞的125I衰变与每个细胞的致死损伤(减去自然对数存活)以及洗脱水平之间的线性关系。利用校准数据计算得出,对于大于6 Gy的剂量,两种细胞类型经X射线照射后DNA双链断裂的产率为每戈瑞每道尔顿DNA 6至9×10(-12)个DNA双链断裂。X射线照射和125I标记细胞的中性滤膜洗脱和存活数据表明,两种细胞类型的致死损伤与DNA双链断裂之间的关系存在显著差异。曾尝试研究125I诱导的DNA双链断裂的修复动力学,但由于在经历冻融过程而死亡的细胞中发生的快速DNA降解而受阻。

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