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彗星试验:机制与技术考量

The comet assay: mechanisms and technical considerations.

作者信息

Klaude M, Eriksson S, Nygren J, Ahnström G

机构信息

Department of Radiobiology, Stockholm University, Sweden.

出版信息

Mutat Res. 1996 Jun 12;363(2):89-96. doi: 10.1016/0921-8777(95)00063-1.

Abstract

The comet assay is frequently used to measure DNA damage in individual cells. In order to better understand the mechanisms behind the technique, we have studied the behaviour of DNA under different electrophoresis conditions in mammalian cells exposed to gamma radiation. The comet tails obtained after neutral electrophoresis seem to consist of DNA loops which are attached to structures in the nucleus, since the DNA cannot move in the second direction after two-dimensional electrophoresis. When the DNA is labelled by a short pulse, microautoradiography reveals that all label appear in the head of the comets when neutral electrophoresis is applied. After chase incubation, the label moves out into the tails. This gives further support to the view that the DNA loops are fixed to some structure in the nucleus where also the DNA synthesis takes place. Under alkaline electrophoresis conditions, however, the entire comet tails move in the new electrophoresis direction. Thus, it appears that the alkaline comet tails consist of free DNA fragments. Further, the effects of alkaline concentration and sodium chloride during unwinding and electrophoresis are discussed. Throughout the study, a protocol for drying and fixation of the comets has been used.

摘要

彗星试验常用于检测单个细胞中的DNA损伤。为了更好地理解该技术背后的机制,我们研究了在受到γ辐射的哺乳动物细胞中,不同电泳条件下DNA的行为。中性电泳后得到的彗星尾似乎由附着于细胞核内结构的DNA环组成,因为在二维电泳后DNA无法在第二个方向移动。当DNA用短脉冲标记时,微放射自显影显示,进行中性电泳时,所有标记都出现在彗星头部。追踪孵育后,标记移至尾部。这进一步支持了DNA环固定于细胞核内DNA合成发生处的某些结构的观点。然而,在碱性电泳条件下,整个彗星尾在新的电泳方向上移动。因此,碱性彗星尾似乎由游离的DNA片段组成。此外,还讨论了在解旋和电泳过程中碱性浓度和氯化钠的影响。在整个研究过程中,采用了一种彗星干燥和固定的方案。

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